General Information of the m6A Regulator (ID: REG00014)
Regulator Name Insulin-like growth factor 2 mRNA-binding protein 3 (IGF2BP3)
Synonyms
IGF2 mRNA-binding protein 3; IMP-3; IGF-II mRNA-binding protein 3; KH domain-containing protein overexpressed in cancer; hKOC; VICKZ family member 3; IMP3; KOC1; VICKZ3
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Gene Name IGF2BP3
Sequence
MNKLYIGNLSENAAPSDLESIFKDAKIPVSGPFLVKTGYAFVDCPDESWALKAIEALSGK
IELHGKPIEVEHSVPKRQRIRKLQIRNIPPHLQWEVLDSLLVQYGVVESCEQVNTDSETA
VVNVTYSSKDQARQALDKLNGFQLENFTLKVAYIPDEMAAQQNPLQQPRGRRGLGQRGSS
RQGSPGSVSKQKPCDLPLRLLVPTQFVGAIIGKEGATIRNITKQTQSKIDVHRKENAGAA
EKSITILSTPEGTSAACKSILEIMHKEAQDIKFTEEIPLKILAHNNFVGRLIGKEGRNLK
KIEQDTDTKITISPLQELTLYNPERTITVKGNVETCAKAEEEIMKKIRESYENDIASMNL
QAHLIPGLNLNALGLFPPTSGMPPPTSGPPSAMTPPYPQFEQSETETVHLFIPALSVGAI
IGKQGQHIKQLSRFAGASIKIAPAEAPDAKVRMVIITGPPEAQFKAQGRIYGKIKEENFV
SPKEEVKLEAHIRVPSFAAGRVIGKGGKTVNELQNLSSAEVVVPRDQTPDENDQVVVKIT
GHFYACQVAQRKIQEILTQVKQHQQQKALQSGPPQSRRK
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Family RRM IMP/VICKZ family
Function
RNA-binding factor that may recruit target transcripts to cytoplasmic protein-RNA complexes (mRNPs). This transcript 'caging' into mRNPs allows mRNA transport and transient storage. It also modulates the rate and location at which target transcripts encounter the translational apparatus and shields them from endonuclease attacks or microRNA-mediated degradation. Binds to the 3'-UTR of CD44 mRNA and stabilizes it, hence promotes cell adhesion and invadopodia formation in cancer cells. Binds to beta-actin/ACTB and MYC transcripts. Binds to the 5'-UTR of the insulin-like growth factor 2 (IGF2) mRNAs.
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Gene ID 10643
Uniprot ID
IF2B3_HUMAN
Regulator Type WRITER ERASER READER
Mechanism Diagram Click to View the Original Diagram
Target Genes Click to View Potential Target Genes of This Regulator
Full List of Target Gene(s) of This m6A Regulator and Corresponding Disease/Drug Response(s)
IGF2BP3 can regulate the m6A methylation of following target genes, and result in corresponding disease/drug response(s). You can browse corresponding disease or drug response(s) resulted from the regulation of certain target gene.
Browse Target Gene related Disease
Browse Target Gene related Drug
ATP-dependent translocase ABCB1 (ABCB1)
Representative RNA-seq result indicating the expression of this target gene regulated by IGF2BP3
Cell Line ES-2 cell line Homo sapiens
Treatment: siIGF2BP3 ES-2 cells
Control: siControl ES-2 cells
GSE109604
Regulation
logFC: -1.30E+00
p-value: 4.65E-03
More Results Click to View More RNA-seq Results
Colorectal cancer [ICD-11: 2B91]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [1]
Responsed Disease Colorectal cancer [ICD-11: 2B91]
Responsed Drug Doxil Approved
Target Regulation Up regulation
Pathway Response ABC transporters hsa02010
Cell Process RNA stability
In-vitro Model
DLD-1 Colon adenocarcinoma Homo sapiens CVCL_0248
HCT 116 Colon carcinoma Homo sapiens CVCL_0291
HCT 15 Colon adenocarcinoma Homo sapiens CVCL_0292
HCT 8 Colon adenocarcinoma Homo sapiens CVCL_2478
HT29 Colon cancer Mus musculus CVCL_A8EZ
SW1463 Rectal adenocarcinoma Homo sapiens CVCL_1718
SW480 Colon adenocarcinoma Homo sapiens CVCL_0546
SW620 Colon adenocarcinoma Homo sapiens CVCL_0547
In-vivo Model HCT8/T xenografts derived from shNC or shIGF2BP3-1 HCT8/T cells were established through subcutaneous inoculation of cells (6×106) into nude mice.
Response Summary IGF2BP3, directly bound to the m6A-modified region of ATP-dependent translocase ABCB1 (ABCB1) mRNA, thereby promoting the stability and expression of ABCB1 mRNA. The expression of IGF2BP3 and ABCB1 was strongly correlated with DOX sensitivity. Targeting IGF2BP3 was an important chemotherapeutic strategy for preventing MDR development in colorectal cancer.
Bax inhibitor 1 (TMBIM6)
Representative RNA-seq result indicating the expression of this target gene regulated by IGF2BP3
Cell Line ES-2 cell line Homo sapiens
Treatment: siIGF2BP3 ES-2 cells
Control: siControl ES-2 cells
GSE109604
Regulation
logFC: -8.65E-01
p-value: 2.88E-02
More Results Click to View More RNA-seq Results
Laryngeal cancer [ICD-11: 2C23]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [2]
Responsed Disease Laryngeal cancer [ICD-11: 2C23]
Target Regulation Up regulation
Cell Process RNA stability
Cell apoptosis
In-vitro Model
AMC-HN-8 Laryngeal squamous cell carcinoma Homo sapiens CVCL_5966
NHBEC (Normal human bronchial epithelial cell)
Tu 177 Laryngeal squamous cell carcinoma Homo sapiens CVCL_4913
Tu 212 Head and neck squamous cell carcinoma Homo sapiens CVCL_4915
In-vivo Model For tumor growth studies, whether in vivo RBM15 knockdown/overexpression experiments or in vivo rescue experiments, each group included six mice. Each mouse was injected with 100 uL of lentivirus-transfected tumor cells.
Response Summary RBM15-mediated m6A modification of Bax inhibitor 1 (TMBIM6) mRNA enhanced TMBIM6 stability through IGF2BP3-dependent. Laryngeal squamous cell cancer cells were transfected with shRBM15 lentivirus for 48h, and the qRT-PCR data indicated that the mRNA levels of CPNE5, TMBIM6, and ATAD3A decreased after RBM15 knockdown.
Hepatoma-derived growth factor (HDGF)
Representative RNA-seq result indicating the expression of this target gene regulated by IGF2BP3
Cell Line ES-2 cell line Homo sapiens
Treatment: siIGF2BP3 ES-2 cells
Control: siControl ES-2 cells
GSE109604
Regulation
logFC: -6.81E-01
p-value: 1.47E-02
More Results Click to View More RNA-seq Results
Gastric cancer [ICD-11: 2B72]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [3]
Responsed Disease Gastric cancer [ICD-11: 2B72]
Target Regulation Up regulation
Pathway Response Glycolysis / Gluconeogenesis hsa00010
Cell Process Glycolysis
In-vitro Model
HGC-27 Gastric carcinoma Homo sapiens CVCL_1279
NCI-N87 Gastric tubular adenocarcinoma Homo sapiens CVCL_1603
SGC-7901 Gastric carcinoma Homo sapiens CVCL_0520
In-vivo Model Mice 8 weeks after splenic portal vein injection of BGC823 cells with METTL3 overexpression or vector-transfected cells.
Response Summary Elevated METTL3 expression promotes tumour angiogenesis and glycolysis in Gastric cancer. P300-mediated H3K27 acetylation activation in the promoter of METTL3 induced METTL3 transcription, which stimulated m6A modification of Hepatoma-derived growth factor (HDGF) mRNA, and the m6A reader IGF2BP3 then directly recognised and bound to the m6A site on HDGF mRNA and enhanced HDGF mRNA stability.
MARCKS-related protein (MARCKSL1)
Representative RIP-seq result supporting the interaction between the target gene and IGF2BP3
Cell Line HEK293T Homo sapiens
Regulation logFC: 1.28E+00 GSE90639
Liver cancer [ICD-11: 2C12]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [4]
Responsed Disease Hepatocellular carcinoma [ICD-11: 2C12.02]
Cell Process RNA decay
In-vitro Model
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
HEK293T Normal Homo sapiens CVCL_0063
HeLa Endocervical adenocarcinoma Homo sapiens CVCL_0030
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
Response Summary In contrast to the mRNA-decay-promoting function of YTH domain-containing family protein 2, IGF2BPs promote the stability and storage of their target mRNAs (for example, MYC) in an m6A-dependent manner under normal and stress conditions and therefore affect gene expression output. Four representative high confidence targets, including MYC, FSCN1, TK1, and MARCKS-related protein (MARCKSL1), exhibit strong binding with IGF2BPs around their m6A motifs in control cells. Knocking down of each individual IGF2BPs in Hela (cervical cancer) and HepG2 (liver cancer) cells significantly repressed MYC expression.
Cervical cancer [ICD-11: 2C77]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [4]
Responsed Disease Cervical cancer [ICD-11: 2C77]
Cell Process RNA decay
In-vitro Model
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
HEK293T Normal Homo sapiens CVCL_0063
HeLa Endocervical adenocarcinoma Homo sapiens CVCL_0030
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
Response Summary In contrast to the mRNA-decay-promoting function of YTH domain-containing family protein 2, IGF2BPs promote the stability and storage of their target mRNAs (for example, MYC) in an m6A-dependent manner under normal and stress conditions and therefore affect gene expression output. Four representative high confidence targets, including MYC, FSCN1, TK1, and MARCKS-related protein (MARCKSL1), exhibit strong binding with IGF2BPs around their m6A motifs in control cells. Knocking down of each individual IGF2BPs in Hela (cervical cancer) and HepG2 (liver cancer) cells significantly repressed MYC expression.
Protein RCC2 (RCC2)
Representative RIP-seq result supporting the interaction between the target gene and IGF2BP3
Cell Line HEK293T Homo sapiens
Regulation logFC: 1.30E+00 GSE90639
Acute myeloid leukaemia [ICD-11: 2A60]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [5]
Responsed Disease Acute myeloid leukaemia [ICD-11: 2A60]
Target Regulation Up regulation
Cell Process Cell apoptosis
In-vitro Model
THP-1 Childhood acute monocytic leukemia Homo sapiens CVCL_0006
SUP-B15 B-lymphoblastic leukemia Homo sapiens CVCL_0103
KG-1 Adult acute myeloid leukemia Homo sapiens CVCL_0374
K-562 Chronic myelogenous leukemia Homo sapiens CVCL_0004
HL-60 Adult acute myeloid leukemia Homo sapiens CVCL_0002
Response Summary IGF2BP3 is required for maintaining AML cell survival in an m6A-dependent manner, and knockdown of IGF2BP3 dramatically suppresses the apoptosis, reduces the proliferation, and impairs the leukemic capacity of AML cells in vitro and in vivo.IGF2BP3 interacts with Protein RCC2 (RCC2) mRNA and stabilizes the expression of m6A-modified RNA.
Y-box-binding protein 1 (YBX1)
Representative RIP-seq result supporting the interaction between the target gene and IGF2BP3
Cell Line HEK293T Homo sapiens
Regulation logFC: 2.22E+00 GSE90639
Malignant haematopoietic neoplasm [ICD-11: 2B33]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [6]
Responsed Disease Myeloid leukaemia [ICD-11: 2B33.1]
Target Regulation Up regulation
Cell Process Cell apoptosis
In-vitro Model
Leukemia stem cell line (Leukemia stem cell line)
Kasumi-1 Myeloid leukemia with maturation Homo sapiens CVCL_0589
MOLM-13 Adult acute myeloid leukemia Homo sapiens CVCL_2119
THP-1 Childhood acute monocytic leukemia Homo sapiens CVCL_0006
MV4-11 Childhood acute monocytic leukemia Homo sapiens CVCL_0064
BV-173 Chronic myelogenous leukemia Homo sapiens CVCL_0181
NOMO-1 Adult acute monocytic leukemia Homo sapiens CVCL_1609
K-562 Chronic myelogenous leukemia Homo sapiens CVCL_0004
KG-1a Adult acute myeloid leukemia Homo sapiens CVCL_1824
Response Summary Y-box-binding protein 1 (YBX1) selectively functions in regulating survival of myeloid leukemia cells. YBX1 interacts with insulin-like growth factor 2 messenger RNA (mRNA)-binding proteins (IGF2BPs) and stabilizes m6A-tagged RNA. YBX1 deficiency dysregulates the expression of apoptosis-related genes and promotes mRNA decay of MYC and BCL2 in an m6A-dependent manner, which contributes to the defective survival that results from deletion of YBX1.
Metastasis associated lung adenocarcinoma transcript 1 (MALAT1)
Representative RIP-seq result supporting the interaction between the target gene and IGF2BP3
Cell Line HEK293T Homo sapiens
Regulation logFC: 2.96E+00 GSE90639
Atopic eczema [ICD-11: EA80]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [7]
Responsed Disease Atopic eczema [ICD-11: EA80]
Target Regulation Up regulation
Pathway Response MAPK signaling pathway hsa04010
Ubiquitin mediated proteolysis hsa04120
Cell Process Inflammation
Proteasome pathway degradation
In-vitro Model
RAW 264.7 Mouse leukemia Mus musculus CVCL_0493
In-vivo Model IMQ-induced psoriatic model was constructed by applying 10 mg per ear 5% IMQ for 8 consecutive days, and 6 ug macrophage-specific control or hsa_circ_0004287 plasmid was topically applied every 2 days (5 mice per group per experiment).
Response Summary CircRNA hsa_circ_0004287 was upregulated in peripheral blood mononuclear cells of both AD and psoriasis patients. hsa_circ_0004287 reduced the stability of its host gene Metastasis associated lung adenocarcinoma transcript 1 (MALAT1) by competitively binding to IGF2BP3 with MALAT1 in an N6-methyladenosine (m6A)-dependent manner.
Apoptosis regulator Bcl-2 (BCL2)
Malignant haematopoietic neoplasm [ICD-11: 2B33]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [6]
Responsed Disease Myeloid leukaemia [ICD-11: 2B33.1]
Target Regulation Up regulation
Cell Process Cell apoptosis
In-vitro Model
Leukemia stem cell line (Leukemia stem cell line)
Kasumi-1 Myeloid leukemia with maturation Homo sapiens CVCL_0589
MOLM-13 Adult acute myeloid leukemia Homo sapiens CVCL_2119
THP-1 Childhood acute monocytic leukemia Homo sapiens CVCL_0006
MV4-11 Childhood acute monocytic leukemia Homo sapiens CVCL_0064
BV-173 Chronic myelogenous leukemia Homo sapiens CVCL_0181
NOMO-1 Adult acute monocytic leukemia Homo sapiens CVCL_1609
K-562 Chronic myelogenous leukemia Homo sapiens CVCL_0004
KG-1a Adult acute myeloid leukemia Homo sapiens CVCL_1824
Response Summary YBX1 selectively functions in regulating survival of myeloid leukemia cells. YBX1 interacts with insulin-like growth factor 2 messenger RNA (mRNA)-binding proteins (IGF2BPs) and stabilizes m6A-tagged RNA. YBX1 deficiency dysregulates the expression of apoptosis-related genes and promotes mRNA decay of MYC and Apoptosis regulator Bcl-2 (BCL2) in an m6A-dependent manner, which contributes to the defective survival that results from deletion of YBX1.
Apoptotic chromatin condensation inducer in the nucleus (ACIN1)
Cervical cancer [ICD-11: 2C77]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [8]
Responsed Disease Cervical cancer [ICD-11: 2C77]
Target Regulation Up regulation
Pathway Response mRNA surveillance pathway hsa03015
RNA degradation hsa03018
Cell Process RNA stability
In-vitro Model
SiHa Cervical squamous cell carcinoma Homo sapiens CVCL_0032
HeLa Endocervical adenocarcinoma Homo sapiens CVCL_0030
End1/E6E7 Normal Homo sapiens CVCL_3684
In-vivo Model 2 × 106 stably transfected HeLa cells were subcutaneously inoculated into the left flank of mice.
Response Summary METTL3 interacts with IGF2BP3 to promote the mRNA stability of Apoptotic chromatin condensation inducer in the nucleus (ACIN1), the overexpression of which induces the aggressiveness of CC cells.
Autophagy protein 5 (ATG5)
Osteosarcoma [ICD-11: 2B51]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [9]
Responsed Disease Osteosarcoma [ICD-11: 2B51]
Responsed Drug Spautin 1 Preclinical
Target Regulation Up regulation
In-vivo Model For tumor growth assay, 2 × 106 OS cells in 100 μL medium were injected into the nude mice subcutaneously. For tumor metastasis assay, we injected medium containing 2 × 106 cells through the caudal vein. An IVIS200 imaging system (Caliper Life Science, USA) was used to image and assess the OS metastasis. For pharmacological inhibition of USP13, mice bearing xenografts were treated with Spautin-1 (40 mg/kg/day i.p.) or vehicle for 2 weeks.
Catenin beta-1 (CTNNB1/Beta-catenin)
Chronic kidney disease [ICD-11: GB61]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [10]
Responsed Disease Chronic kidney disease [ICD-11: GB61]
In-vitro Model
HK-2 [Human kidney] Normal Homo sapiens CVCL_0302
In-vivo Model Mice were injected with empty vector (pcDNA3) or Flag-tagged METTL3 expression vector (pFlag-METTL3) at 2 days after UUO or 4 days after UIRI, respectively. The expression of transgene was validated by Western blotting or immunostaining for Flag-tagged METTL3 fusion protein.
CD44 antigen (CD44)
Renal cell carcinoma [ICD-11: 2C90]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [11]
Responsed Disease Renal cell carcinoma [ICD-11: 2C90]
Responsed Drug Sunitinib Approved
In-vitro Model
ACHN Papillary renal cell carcinoma Homo sapiens CVCL_1067
A-498 Renal cell carcinoma Homo sapiens CVCL_1056
Caki-1 Clear cell renal cell carcinoma Homo sapiens CVCL_0234
OS-RC-2 Clear cell renal cell carcinoma Homo sapiens CVCL_1626
786-O Renal cell carcinoma Homo sapiens CVCL_1051
HK-2 [Human kidney] Normal Homo sapiens CVCL_0302
In-vivo Model A total of 1 × 106 ACHN cells was injected into left renal capsule (n = 5 mice/group). Then, we sutured the wound layer by layer. Tumour size was measured 4 weeks later with in-Vivo FX PRO small animal imaging system (BRUKER). After that, we executed the mice and collected tumours for immunohistochemistry (IHC) assays and Western blotting. For metastasis model construction, 1 × 106 ACHN cells were injected into tail-vein of each mouse (n = 5 mice/group).
Complex I-AGGG (NDUFB2)
Lung cancer [ICD-11: 2C25]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [12]
Responsed Disease Non-small-cell lung carcinoma [ICD-11: 2C25.Y]
Target Regulation Down regulation
Pathway Response Ubiquitin mediated proteolysis hsa04120
Cell Process Tumour immunology
Ubiquitination degradation
In-vitro Model
A-549 Lung adenocarcinoma Homo sapiens CVCL_0023
BEAS-2B Normal Homo sapiens CVCL_0168
NCI-H1299 Lung large cell carcinoma Homo sapiens CVCL_0060
NCI-H1650 Minimally invasive lung adenocarcinoma Homo sapiens CVCL_1483
NCI-H1703 Lung squamous cell carcinoma Homo sapiens CVCL_1490
NCI-H1975 Lung adenocarcinoma Homo sapiens CVCL_1511
NCI-H460 Lung large cell carcinoma Homo sapiens CVCL_0459
HCC827 Lung adenocarcinoma Homo sapiens CVCL_2063
LL/2 (LLC1) Malignant tumors Mus musculus CVCL_4358
In-vivo Model A549 cells were transfected with the pZW1-FCS-circNDUFB2 plasmid or pZW1-FCS-Vector plasmid, and selected with G418 (800 ug/ml) for 4 weeks, and then 2 × 106 A549 cells were subcutaneously injected into the right flank of each mouse.
Response Summary Complex I-AGGG (NDUFB2) interacts with IGF2BP1/2/3 in NSCLC cells. circNDUFB2 participates in the degradation of IGF2BPs and activation of anti-tumor immunity during NSCLC progression via the modulation of both protein ubiquitination and degradation, as well as cellular immune responses.
Cyclin-dependent kinase 4 (CDK4)
Renal cell carcinoma [ICD-11: 2C90]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [13]
Responsed Disease Renal cell carcinoma of kidney [ICD-11: 2C90.0]
Target Regulation Up regulation
Pathway Response Cell cycle hsa04110
Cell Process Accelerating the G1-S transition
Cell invasion and metastasis
In-vitro Model
769-P Renal cell carcinoma Homo sapiens CVCL_1050
786-O Renal cell carcinoma Homo sapiens CVCL_1051
ACHN Papillary renal cell carcinoma Homo sapiens CVCL_1067
Caki-1 Clear cell renal cell carcinoma Homo sapiens CVCL_0234
In-vivo Model Stable DMDRMR knockdown (KD) and control cell lines were injected subcutaneously (s.c.; 1 × 107 cells/inoculum) into the flanks of recipient NOD/SCID/IL2Rγ-null (NSG) mice.
Response Summary DMDRMR is a protumorigenic lncRNA that mediates the stabilization of IGF2BP3 targets in an m6A-dependent manner in clear cell renal cell carcinoma. IGF2BP3 and DMDRMR cooperate to play oncogenic roles. IGF2BP3 cooperates with DMDRMR to regulate Cyclin-dependent kinase 4 (CDK4) by enhancing mRNA stability.
Cystine/glutamate transporter (SLC7A11)
Liver cancer [ICD-11: 2C12]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [14]
Responsed Disease Liver cancer [ICD-11: 2C12]
Target Regulation Up regulation
DNA replication licensing factor MCM5 (MCM5)
Lung cancer [ICD-11: 2C25]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [15]
Responsed Disease Lung adenocarcinoma [ICD-11: 2C25.0]
Target Regulation Up regulation
In-vitro Model
HEK293-FT Normal Homo sapiens CVCL_6911
In-vivo Model Female BALB/c-nu mice (6-8 weeks of age, 18-20 g) were used to investigate the pro-invasive and pro-metastatic effects of IGF2BP3 and MCM5. To assess local invasion, indicated cells were injected subcutaneously into the flanks of mice (1 × 106 cells suspended in 100 μL sterile PBS, A549-Vector left and A549-IGF2BP3 or A549-MCM5 right, n = 5), and the number of mice with local invasion was counted. To determine distant lung dissemination, 1 × 106 indicated cells were injected into the lateral tail vein (n = 5), and metastases were monitored and analyzed by bioluminescent imaging assisted with Spectrum Living Image 4.0 software (Caliper Life Sciences, Hopkinton, MA, USA). Alternatively, vector control or IGF2BP3-overexpressing A549 cells (5 × 105) were intracardiacally injected. At the indicated experimental endpoints, mice were anesthetized and sacrificed, and lung tissues were fixed in picric acid containing 4% formaldehyde. Subcutaneous tumors and lung tissues were resected, sectioned (5 mm in thickness) and histologically examined by H&E staining.
Ephrin type-A receptor 2 (EphA2)
Colorectal cancer [ICD-11: 2B91]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [16]
Responsed Disease Colorectal cancer [ICD-11: 2B91]
Target Regulation Up regulation
Pathway Response PI3K-Akt signaling pathway hsa04151
In-vitro Model
SW620 Colon adenocarcinoma Homo sapiens CVCL_0547
SW480 Colon adenocarcinoma Homo sapiens CVCL_0546
NCM460 Normal Homo sapiens CVCL_0460
LoVo Colon adenocarcinoma Homo sapiens CVCL_0399
HT29 Colon cancer Mus musculus CVCL_A8EZ
HCT 116 Colon carcinoma Homo sapiens CVCL_0291
DLD-1 Colon adenocarcinoma Homo sapiens CVCL_0248
In-vivo Model A total of 8 × 106 wild-type (WT) or METTL3-knockdown cells were injected into the dorsal flanks of 6-week-old nude mice. Seven mice were randomly selected to calculate the volume according to the following formula: V = (width2 × length)/2. Mice were euthanized three weeks after injection and tumors removed, weighed, fixed, and embedded for immunohistochemical analysis.
Response Summary Ephrin type-A receptor 2 (EphA2) and VEGFA targeted by METTL3 via different IGF2BP3-dependent mechanisms were found to promote vasculogenic mimicry (VM) formation via PI3K/AKT/mTOR and ERK1/2 signaling in CRC.
Fascin (FSCN1)
Liver cancer [ICD-11: 2C12]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [4]
Responsed Disease Hepatocellular carcinoma [ICD-11: 2C12.02]
Cell Process RNA decay
In-vitro Model
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
HEK293T Normal Homo sapiens CVCL_0063
HeLa Endocervical adenocarcinoma Homo sapiens CVCL_0030
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
Response Summary In contrast to the mRNA-decay-promoting function of YTH domain-containing family protein 2, IGF2BPs promote the stability and storage of their target mRNAs (for example, MYC) in an m6A-dependent manner under normal and stress conditions and therefore affect gene expression output. Four representative high confidence targets, including MYC, Fascin (FSCN1), TK1, and MARCKSL1, exhibit strong binding with IGF2BPs around their m6A motifs in control cells. Knocking down of each individual IGF2BPs in Hela (cervical cancer) and HepG2 (liver cancer) cells significantly repressed MYC expression.
Cervical cancer [ICD-11: 2C77]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [4]
Responsed Disease Cervical cancer [ICD-11: 2C77]
Cell Process RNA decay
In-vitro Model
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
HEK293T Normal Homo sapiens CVCL_0063
HeLa Endocervical adenocarcinoma Homo sapiens CVCL_0030
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
Response Summary In contrast to the mRNA-decay-promoting function of YTH domain-containing family protein 2, IGF2BPs promote the stability and storage of their target mRNAs (for example, MYC) in an m6A-dependent manner under normal and stress conditions and therefore affect gene expression output. Four representative high confidence targets, including MYC, Fascin (FSCN1), TK1, and MARCKSL1, exhibit strong binding with IGF2BPs around their m6A motifs in control cells. Knocking down of each individual IGF2BPs in Hela (cervical cancer) and HepG2 (liver cancer) cells significantly repressed MYC expression.
Glucose transporter type 1 (GLUT1)
Head and neck squamous carcinoma [ICD-11: 2B6E]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [17]
Responsed Disease Oral squamous cell carcinoma [ICD-11: 2B6E.0]
Target Regulation Up regulation
Colorectal cancer [ICD-11: 2B91]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [18]
Responsed Disease Colorectal cancer [ICD-11: 2B91]
Target Regulation Up regulation
Pathway Response Glycolysis / Gluconeogenesis hsa00010
Cell Process Glucose metabolism
Response Summary METTL3 stabilizes HK2 and Glucose transporter type 1 (SLC2A1) (GLUT1) expression in colorectal cancer through an m6A-IGF2BP2/3- dependent mechanism.
Hexokinase-2 (HK2)
Colorectal cancer [ICD-11: 2B91]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [18]
Responsed Disease Colorectal cancer [ICD-11: 2B91]
Target Regulation Up regulation
Pathway Response Glycolysis / Gluconeogenesis hsa00010
Cell Process Glucose metabolism
Response Summary METTL3 stabilizes Hexokinase-2 (HK2) and SLC2A1 (GLUT1) expression in colorectal cancer through an m6A-IGF2BP2/3- dependent mechanism.
High mobility group protein B1 (HMGB1)
Bladder cancer [ICD-11: 2C94]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [19]
Responsed Disease Bladder cancer [ICD-11: 2C94]
Target Regulation Up regulation
High mobility group protein HMGI-C (HMGA2)
Renal cell carcinoma [ICD-11: 2C90]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [11]
Responsed Disease Renal cell carcinoma [ICD-11: 2C90]
Responsed Drug Sunitinib Approved
In-vitro Model
ACHN Papillary renal cell carcinoma Homo sapiens CVCL_1067
A-498 Renal cell carcinoma Homo sapiens CVCL_1056
Caki-1 Clear cell renal cell carcinoma Homo sapiens CVCL_0234
OS-RC-2 Clear cell renal cell carcinoma Homo sapiens CVCL_1626
786-O Renal cell carcinoma Homo sapiens CVCL_1051
HK-2 [Human kidney] Normal Homo sapiens CVCL_0302
In-vivo Model A total of 1 × 106 ACHN cells was injected into left renal capsule (n = 5 mice/group). Then, we sutured the wound layer by layer. Tumour size was measured 4 weeks later with in-Vivo FX PRO small animal imaging system (BRUKER). After that, we executed the mice and collected tumours for immunohistochemistry (IHC) assays and Western blotting. For metastasis model construction, 1 × 106 ACHN cells were injected into tail-vein of each mouse (n = 5 mice/group).
Hypoxia-inducible factor 1-alpha (HIF-1-Alpha/HIF1A)
Gastric cancer [ICD-11: 2B72]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [20]
Responsed Disease Gastric cancer [ICD-11: 2B72]
Target Regulation Up regulation
Cell Process Cell migration
In-vitro Model
MKN45 Gastric adenocarcinoma Homo sapiens CVCL_0434
HUVEC-C Normal Homo sapiens CVCL_2959
HGC-27 Gastric carcinoma Homo sapiens CVCL_1279
Response Summary IGF2BP3 positively regulated Hypoxia-inducible factor 1-alpha (HIF-1-Alpha/HIF1A) expression by directly binding to a specific m6A site in the coding region of HIF1A mRNA in gastric cancer cells. IGF2BP3 and HIF1A were highly expressed in GC tissues and hypoxia-treated GC cells.
Certain specified diseases of liver [ICD-11: DB99]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [21]
Responsed Disease Certain specified diseases of liver [ICD-11: DB99.7]
Target Regulation Up regulation
In-vitro Model
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
Hep 3B2.1-7 Childhood hepatocellular carcinoma Homo sapiens CVCL_0326
Intercellular adhesion molecule 1 (ICAM1)
Thyroid Cancer [ICD-11: 2D10]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [22]
Responsed Disease Thyroid Cancer [ICD-11: 2D10]
L-glutamine amidohydrolase (GLS2)
Cervical cancer [ICD-11: 2C77]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [23]
Responsed Disease Cervical cancer [ICD-11: 2C77]
Target Regulation Up regulation
Myc proto-oncogene protein (MYC)
Brain cancer [ICD-11: 2A00]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [24]
Responsed Disease Glioma [ICD-11: 2A00.0]
Responsed Drug Linsitinib Phase 3
Target Regulation Up regulation
Pathway Response RNA degradation hsa03018
Cell Process RNA stability
In-vitro Model
()
HNP1 (A human neural progenitor cell)
NHA (Normal human astrocytes)
NSC11 (Pluripotent derived neural progenitor cell)
In-vivo Model For in vivo drug treatment studies, intracranial xenografts were generated by implanting 5000 patient-derived GSCs (387 and 4121) into the right cerebral cortex of NSG mice as described above.
Response Summary The m6A reader YTHDF2 stabilized Myc proto-oncogene protein (MYC) mRNA specifically in cancer stem cells. Given the challenge of targeting MYC, YTHDF2 presents a therapeutic target to perturb MYC signaling in glioblastoma. The IGF1/IGF1R inhibitor linsitinib preferentially targeted YTHDF2-expressing cells, inhibiting GSC viability without affecting NSCs and impairing in vivo glioblastoma growth. YTHDF2 links RNA epitranscriptomic modifications and GSC growth, laying the foundation for the YTHDF2-MYC-IGFBP3 axis as a specific and novel therapeutic target in glioblastoma.
Malignant haematopoietic neoplasm [ICD-11: 2B33]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [6]
Responsed Disease Myeloid leukaemia [ICD-11: 2B33.1]
Target Regulation Up regulation
Cell Process Cell apoptosis
In-vitro Model
Leukemia stem cell line (Leukemia stem cell line)
Kasumi-1 Myeloid leukemia with maturation Homo sapiens CVCL_0589
MOLM-13 Adult acute myeloid leukemia Homo sapiens CVCL_2119
THP-1 Childhood acute monocytic leukemia Homo sapiens CVCL_0006
MV4-11 Childhood acute monocytic leukemia Homo sapiens CVCL_0064
BV-173 Chronic myelogenous leukemia Homo sapiens CVCL_0181
NOMO-1 Adult acute monocytic leukemia Homo sapiens CVCL_1609
K-562 Chronic myelogenous leukemia Homo sapiens CVCL_0004
KG-1a Adult acute myeloid leukemia Homo sapiens CVCL_1824
Response Summary YBX1 selectively functions in regulating survival of myeloid leukemia cells. YBX1 interacts with insulin-like growth factor 2 messenger RNA (mRNA)-binding proteins (IGF2BPs) and stabilizes m6A-tagged RNA. YBX1 deficiency dysregulates the expression of apoptosis-related genes and promotes mRNA decay of Myc proto-oncogene protein (MYC) and BCL2 in an m6A-dependent manner, which contributes to the defective survival that results from deletion of YBX1.
Gastric cancer [ICD-11: 2B72]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [25]
Responsed Disease Gastric cancer [ICD-11: 2B72]
Target Regulation Up regulation
In-vitro Model
AGS Gastric adenocarcinoma Homo sapiens CVCL_0139
MKN1 Gastric adenosquamous carcinoma Homo sapiens CVCL_1415
SGC-7901 Gastric carcinoma Homo sapiens CVCL_0520
BGC-823 Gastric carcinoma Homo sapiens CVCL_3360
MGC-803 Gastric mucinous adenocarcinoma Homo sapiens CVCL_5334
GES-1 Normal Homo sapiens CVCL_EQ22
In-vivo Model The cell mass (5 × 106) was dissolved in 200 μl PBS and subcutaneously injected into the left side of each mouse.
Liver cancer [ICD-11: 2C12]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [4]
Responsed Disease Hepatocellular carcinoma [ICD-11: 2C12.02]
Cell Process RNA decay
In-vitro Model
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
HEK293T Normal Homo sapiens CVCL_0063
HeLa Endocervical adenocarcinoma Homo sapiens CVCL_0030
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
Response Summary In contrast to the mRNA-decay-promoting function of YTH domain-containing family protein 2, IGF2BPs promote the stability and storage of their target mRNAs (for example, MYC) in an m6A-dependent manner under normal and stress conditions and therefore affect gene expression output. Four representative high confidence targets, including Myc proto-oncogene protein (MYC), FSCN1, TK1, and MARCKSL1, exhibit strong binding with IGF2BPs around their m6A motifs in control cells. Knocking down of each individual IGF2BPs in Hela (cervical cancer) and HepG2 (liver cancer) cells significantly repressed MYC expression.
Cervical cancer [ICD-11: 2C77]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [4]
Responsed Disease Cervical cancer [ICD-11: 2C77]
Cell Process RNA decay
In-vitro Model
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
HEK293T Normal Homo sapiens CVCL_0063
HeLa Endocervical adenocarcinoma Homo sapiens CVCL_0030
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
Response Summary In contrast to the mRNA-decay-promoting function of YTH domain-containing family protein 2, IGF2BPs promote the stability and storage of their target mRNAs (for example, MYC) in an m6A-dependent manner under normal and stress conditions and therefore affect gene expression output. Four representative high confidence targets, including Myc proto-oncogene protein (MYC), FSCN1, TK1, and MARCKSL1, exhibit strong binding with IGF2BPs around their m6A motifs in control cells. Knocking down of each individual IGF2BPs in Hela (cervical cancer) and HepG2 (liver cancer) cells significantly repressed MYC expression.
Myt1 kinase (PKMYT1)
Gastric cancer [ICD-11: 2B72]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [26]
Responsed Disease Gastric cancer [ICD-11: 2B72]
Target Regulation Up regulation
Cell Process Cell invasion
Cell migration
In-vitro Model
SGC-7901 Gastric carcinoma Homo sapiens CVCL_0520
HGC-27 Gastric carcinoma Homo sapiens CVCL_1279
BGC-823 Gastric carcinoma Homo sapiens CVCL_3360
In-vivo Model After randomly assignment and anesthetization, nude mice were injected with 5 × 106 cells suspended in 100 uL PBS into the tail vein (n = 5 per group).
Response Summary Myt1 kinase (PKMYT1), as a downstream target of ALKBH5, promoted invasion and migration in GC. Moreover IGF2BP3 helped stabilize the mRNA stability of PKMYT1 via its m6A modification site.
NAD-dependent protein deacetylase sirtuin-1 (SIRT1)
Presbycusis [ICD-11: AB54]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [27]
Responsed Disease Presbycusis [ICD-11: AB54]
Target Regulation Up regulation
Programmed cell death 1 ligand 1 (CD274/PD-L1)
Breast cancer [ICD-11: 2C60]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [28]
Responsed Disease Breast cancer [ICD-11: 2C60]
Target Regulation Up regulation
Pathway Response PD-L1 expression and PD-1 checkpoint pathway in cancer hsa05235
Cell Process Tumor immune escape
In-vitro Model
SK-BR-3 Breast adenocarcinoma Homo sapiens CVCL_0033
MDA-MB-231 Breast adenocarcinoma Homo sapiens CVCL_0062
MCF-10A Normal Homo sapiens CVCL_0598
HCC38 Breast ductal carcinoma Homo sapiens CVCL_1267
4T1 Normal Mus musculus CVCL_0125
In-vivo Model For subcutaneous xenograft experiments in B-NDG mice, approximately 1 × 106 MDA-MB-231 and there was subcutaneous injection of the cells that resuspended in 100 uL PBS into the left flank of the mice and were divided into 11 groups randomly (each containing 5 mice). After the treatment Atezolizumab (Selleck, Shanghai, China) or corresponding iso control antibody (Selleck, Shanghai, China) was injected intratumorally on day 3, 6, 9, 12, 15 post-MDA-MB-231 inoculations, and 5 × 106 cytokine-induced killer (CIK) cells were injected in the tail vein on day 7, 14, 21.
Response Summary Programmed cell death 1 ligand 1 (CD274/PD-L1) was a downstream target of METTL3-mediated m6A modification in breast cancer cells. METTL3-mediated PD-L1 mRNA activation was m6A-IGF2BP3-dependent. PD-L1 expression was also positively correlated with METTL3 and IGF2BP3 expression in breast cancer tissues.
Stearoyl-CoA desaturase (SCD)
Cervical cancer [ICD-11: 2C77]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [29]
Responsed Disease Cervical cancer [ICD-11: 2C77]
In-vitro Model
HeLa Endocervical adenocarcinoma Homo sapiens CVCL_0030
SiHa Cervical squamous cell carcinoma Homo sapiens CVCL_0032
SUMO specific peptidase 1 (SENP1)
Acute myeloid leukaemia [ICD-11: 2A60]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [30]
Responsed Disease Acute myeloid leukaemia [ICD-11: 2A60]
Target Regulation Up regulation
Thymidine kinase, cytosolic (TK1)
Liver cancer [ICD-11: 2C12]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [4]
Responsed Disease Hepatocellular carcinoma [ICD-11: 2C12.02]
Cell Process RNA decay
In-vitro Model
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
HEK293T Normal Homo sapiens CVCL_0063
HeLa Endocervical adenocarcinoma Homo sapiens CVCL_0030
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
Response Summary In contrast to the mRNA-decay-promoting function of YTH domain-containing family protein 2, IGF2BPs promote the stability and storage of their target mRNAs (for example, MYC) in an m6A-dependent manner under normal and stress conditions and therefore affect gene expression output. Four representative high confidence targets, including MYC, FSCN1, Thymidine kinase, cytosolic (TK1), and MARCKSL1, exhibit strong binding with IGF2BPs around their m6A motifs in control cells. Knocking down of each individual IGF2BPs in Hela (cervical cancer) and HepG2 (liver cancer) cells significantly repressed MYC expression.
Cervical cancer [ICD-11: 2C77]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [4]
Responsed Disease Cervical cancer [ICD-11: 2C77]
Cell Process RNA decay
In-vitro Model
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
HEK293T Normal Homo sapiens CVCL_0063
HeLa Endocervical adenocarcinoma Homo sapiens CVCL_0030
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
Response Summary In contrast to the mRNA-decay-promoting function of YTH domain-containing family protein 2, IGF2BPs promote the stability and storage of their target mRNAs (for example, MYC) in an m6A-dependent manner under normal and stress conditions and therefore affect gene expression output. Four representative high confidence targets, including MYC, FSCN1, Thymidine kinase, cytosolic (TK1), and MARCKSL1, exhibit strong binding with IGF2BPs around their m6A motifs in control cells. Knocking down of each individual IGF2BPs in Hela (cervical cancer) and HepG2 (liver cancer) cells significantly repressed MYC expression.
TNF receptor-associated factor 5 (TRAF5)
Liver cancer [ICD-11: 2C12]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [31]
Responsed Disease Liver cancer [ICD-11: 2C12]
Target Regulation Up regulation
In-vitro Model
THLE-3 Normal Homo sapiens CVCL_3804
HCCLM3 Adult hepatocellular carcinoma Homo sapiens CVCL_6832
Hep 3B2.1-7 Childhood hepatocellular carcinoma Homo sapiens CVCL_0326
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
Huh-7 Adult hepatocellular carcinoma Homo sapiens CVCL_0336
Vang-like protein 1 (VANGL1)
Lung cancer [ICD-11: 2C25]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [32]
Responsed Disease Lung adenocarcinoma [ICD-11: 2C25.0]
Target Regulation Up regulation
Pathway Response Nucleotide excision repair hsa03420
Cell Process DNA repair
In-vitro Model
A-549 Lung adenocarcinoma Homo sapiens CVCL_0023
NCI-H1299 Lung large cell carcinoma Homo sapiens CVCL_0060
In-vivo Model Two hundred milliliters of A549 cells (1 × 106) were injected into the left flank of the back of each mouse.
Response Summary Up-regulation of Vang-like protein 1 (VANGL1) by IGF2BPs and miR-29b-3p attenuates the detrimental effect of irradiation on lung adenocarcinoma. Increased m6A level of VANGL1 and reduced miR-29b-3p took the responsibility of VANGL1 overexpression upon irradiation.
Vascular endothelial growth factor A (VEGFA)
Colon cancer [ICD-11: 2B90]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [33]
Responsed Disease Colon cancer [ICD-11: 2B90]
Target Regulation Up regulation
Pathway Response Cell cycle hsa04110
VEGF signaling pathway hsa04370
Cell Process Arrest cell cycle at S phase
In-vitro Model
SW620 Colon adenocarcinoma Homo sapiens CVCL_0547
SW480 Colon adenocarcinoma Homo sapiens CVCL_0546
SW1116 Colon adenocarcinoma Homo sapiens CVCL_0544
RKO Colon carcinoma Homo sapiens CVCL_0504
LoVo Colon adenocarcinoma Homo sapiens CVCL_0399
HT29 Colon cancer Mus musculus CVCL_A8EZ
HCT 116 Colon carcinoma Homo sapiens CVCL_0291
In-vivo Model All the mice (n = 12) were equally and randomly divided into the HCT-scr and HCT-shMETTL3 group. 3 × 106 HCT-scr or HCT-shIGF2BP3 cells suspended in 100 uL PBS were injected subcutaneously from the axilla of each nude mice. After 1 weeks, the long (L) and short (S) diameter of the tumors were measured with vernier caliper every 3 days (tumor volume = L*S2/2). The growth curve of subcutaneous tumors was drawn on the basis of the measured tumor volume. All mice were killed after 17 days since injection of colon cancer cells and subcutaneous tumors were removed completely.
Response Summary Knockdown of IGF2BP3 repressed DNA replication in the S phase of cell cycle and angiogenesis via reading m6A modification of CCND1 and Vascular endothelial growth factor A (VEGFA) respectively. Knockdown of IGF2BP3 repressed angiogenesis in colon cancer via regulating VEGF.
Colorectal cancer [ICD-11: 2B91]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [16]
Responsed Disease Colorectal cancer [ICD-11: 2B91]
Target Regulation Up regulation
Pathway Response PI3K-Akt signaling pathway hsa04151
In-vitro Model
SW620 Colon adenocarcinoma Homo sapiens CVCL_0547
SW480 Colon adenocarcinoma Homo sapiens CVCL_0546
NCM460 Normal Homo sapiens CVCL_0460
LoVo Colon adenocarcinoma Homo sapiens CVCL_0399
HT29 Colon cancer Mus musculus CVCL_A8EZ
HCT 116 Colon carcinoma Homo sapiens CVCL_0291
DLD-1 Colon adenocarcinoma Homo sapiens CVCL_0248
In-vivo Model A total of 8 × 106 wild-type (WT) or METTL3-knockdown cells were injected into the dorsal flanks of 6-week-old nude mice. Seven mice were randomly selected to calculate the volume according to the following formula: V = (width2 × length)/2. Mice were euthanized three weeks after injection and tumors removed, weighed, fixed, and embedded for immunohistochemical analysis.
Response Summary EphA2 and Vascular endothelial growth factor A (VEGFA) targeted by METTL3 via different IGF2BP3-dependent mechanisms were found to promote vasculogenic mimicry (VM) formation via PI3K/AKT/mTOR and ERK1/2 signaling in CRC.
Placental development [ICD-11: XA90F8]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [34]
Responsed Disease Placental development [ICD-11: XA90F8]
In-vitro Model
JEG-3 Gestational choriocarcinoma Homo sapiens CVCL_0363
BeWo Gestational choriocarcinoma Homo sapiens CVCL_0044
HEK293T Normal Homo sapiens CVCL_0063
In-vivo Model Sexually mature mice (older than 8 weeks of age) were mated and the vaginal plugs were confirmed the following morning. The day that a vaginal plug was observed was considered 0.5 days post coitum (0.5 dpc) or embryonic day 0.5 (E0.5). The uterus was cut along the side bearing the embryos and then cut open on the side opposite the placenta. Forceps were used to gently separate the uterus and the maternal surface of the placenta, and then the fetal surface of the placenta and the amniotic sac were separated. Dissected placentas and fetuses were photographed and weighted individually.
KCNMB2 antisense RNA 1 (KCNMB2-AS1)
Cervical cancer [ICD-11: 2C77]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [35]
Responsed Disease Cervical cancer [ICD-11: 2C77]
Target Regulation Up regulation
Cell Process Cell proliferation
Cell apoptosis
In-vitro Model
HeLa Endocervical adenocarcinoma Homo sapiens CVCL_0030
SiHa Cervical squamous cell carcinoma Homo sapiens CVCL_0032
In-vivo Model A total of 1 × 107 control or KCNMB2-AS1-depleted SiHa cells were resuspended in 0.1 ml phosphate-buffered saline and inoculated into the armpit of 5-week-old male BALB/c nude mice.
Response Summary KCNMB2 antisense RNA 1 (KCNMB2-AS1) and IGF2BP3 formed a positive regulatory circuit that enlarged the tumorigenic effect of KCNMB2-AS1 in cervical cancer.
hsa_circ_0004287
Atopic eczema [ICD-11: EA80]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [7]
Responsed Disease Atopic eczema [ICD-11: EA80]
Target Regulation Up regulation
Pathway Response MAPK signaling pathway hsa04010
Ubiquitin mediated proteolysis hsa04120
Cell Process Inflammation
Proteasome pathway degradation
In-vitro Model
RAW 264.7 Mouse leukemia Mus musculus CVCL_0493
In-vivo Model IMQ-induced psoriatic model was constructed by applying 10 mg per ear 5% IMQ for 8 consecutive days, and 6 ug macrophage-specific control or hsa_circ_0004287 plasmid was topically applied every 2 days (5 mice per group per experiment).
Response Summary hsa_circ_0004287 was upregulated in peripheral blood mononuclear cells of both AD and psoriasis patients. hsa_circ_0004287 reduced the stability of its host gene metastasis associated lung adenocarcinoma transcript 1 (MALAT1) by competitively binding to IGF2BP3 with MALAT1 in an N6-methyladenosine (m6A)-dependent manner.
5-hydroxytryptamine receptor 3A (HTR3A)
Esophageal cancer [ICD-11: 2B70]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [36]
Responsed Disease Esophageal Squamous Cell Carcinoma [ICD-11: 2B70.1]
Target Regulation Up regulation
In-vitro Model
KYSE-180 Esophageal squamous cell carcinoma Homo sapiens CVCL_1349
TE-5 Esophageal squamous cell carcinoma Homo sapiens CVCL_1764
KYSE-150 Esophageal squamous cell carcinoma Homo sapiens CVCL_1348
KYSE-510 Esophageal squamous cell carcinoma Homo sapiens CVCL_1354
KYSE-140 Esophageal squamous cell carcinoma Homo sapiens CVCL_1347
Anillin (ANLN)
Placental development [ICD-11: XA90F8]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [34]
Responsed Disease Placental development [ICD-11: XA90F8]
In-vitro Model
JEG-3 Gestational choriocarcinoma Homo sapiens CVCL_0363
BeWo Gestational choriocarcinoma Homo sapiens CVCL_0044
HEK293T Normal Homo sapiens CVCL_0063
In-vivo Model Sexually mature mice (older than 8 weeks of age) were mated and the vaginal plugs were confirmed the following morning. The day that a vaginal plug was observed was considered 0.5 days post coitum (0.5 dpc) or embryonic day 0.5 (E0.5). The uterus was cut along the side bearing the embryos and then cut open on the side opposite the placenta. Forceps were used to gently separate the uterus and the maternal surface of the placenta, and then the fetal surface of the placenta and the amniotic sac were separated. Dissected placentas and fetuses were photographed and weighted individually.
Calpain-15 (CAPN15)
Renal cell carcinoma [ICD-11: 2C90]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [11]
Responsed Disease Renal cell carcinoma [ICD-11: 2C90]
Responsed Drug Sunitinib Approved
In-vitro Model
ACHN Papillary renal cell carcinoma Homo sapiens CVCL_1067
A-498 Renal cell carcinoma Homo sapiens CVCL_1056
Caki-1 Clear cell renal cell carcinoma Homo sapiens CVCL_0234
OS-RC-2 Clear cell renal cell carcinoma Homo sapiens CVCL_1626
786-O Renal cell carcinoma Homo sapiens CVCL_1051
HK-2 [Human kidney] Normal Homo sapiens CVCL_0302
In-vivo Model A total of 1 × 106 ACHN cells was injected into left renal capsule (n = 5 mice/group). Then, we sutured the wound layer by layer. Tumour size was measured 4 weeks later with in-Vivo FX PRO small animal imaging system (BRUKER). After that, we executed the mice and collected tumours for immunohistochemistry (IHC) assays and Western blotting. For metastasis model construction, 1 × 106 ACHN cells were injected into tail-vein of each mouse (n = 5 mice/group).
Claudin-4 (CLDN4)
Gallbladder cancer [ICD-11: 2C13]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [37]
Responsed Disease Gallbladder cancer [ICD-11: 2C13]
Target Regulation Up regulation
Pathway Response NF-kappa B signaling pathway hsa04064
In-vitro Model
GBC-SD Human gallbladder Homo sapiens CVCL_6903
NOZ Gallbladder carcinoma Homo sapiens CVCL_3079
THP-1 Childhood acute monocytic leukemia Homo sapiens CVCL_0006
In-vivo Model NOZ cells (2 × 106 cells) transfected with sh-IGF2BP3 or sh-NC were injected into the flanks of mice (n = 5) according to previously described criteria [23]. After 2 weeks of injection, the tumor volume was measured every 3 days. The tumor volume was calculated by volume = 1 / 2 × long × width2. On day 26, we weighed the tumor.
Collagen alpha-1 (COL6A1)
Renal cell carcinoma [ICD-11: 2C90]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [13]
Responsed Disease Renal cell carcinoma of kidney [ICD-11: 2C90.0]
Target Regulation Up regulation
Cysteine methyltransferase DNMT3A (DNMT3A)
Gastric cancer [ICD-11: 2B72]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [39]
Responsed Disease Gastric cancer [ICD-11: 2B72]
Target Regulation Up regulation
Renal cell carcinoma [ICD-11: 2C90]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [13]
Responsed Disease Renal cell carcinoma of kidney [ICD-11: 2C90.0]
Target Regulation Up regulation
Pathway Response Cell cycle hsa04110
Cell Process Accelerating the G1-S transition
Cell invasion and metastasis
In-vitro Model
769-P Renal cell carcinoma Homo sapiens CVCL_1050
786-O Renal cell carcinoma Homo sapiens CVCL_1051
ACHN Papillary renal cell carcinoma Homo sapiens CVCL_1067
Caki-1 Clear cell renal cell carcinoma Homo sapiens CVCL_0234
In-vivo Model Stable DMDRMR knockdown (KD) and control cell lines were injected subcutaneously (s.c.; 1 × 107 cells/inoculum) into the flanks of recipient NOD/SCID/IL2Rγ-null (NSG) mice.
Response Summary DMDRMR is a protumorigenic lncRNA that mediates the stabilization of IGF2BP3 targets in an m6A-dependent manner in clear cell renal cell carcinoma. IGF2BP3 and DMDRMR cooperate to play oncogenic roles. IGF2BP3 cooperates with DMDRMR to regulate CDK4 by enhancing mRNA stability.
E3 ubiquitin-protein ligase ZNRF3 (ZNRF3)
Brain cancer [ICD-11: 2A00]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [40]
Responsed Disease Brain cancer [ICD-11: 2A00]
Responsed Drug Temozolomide Approved
Target Regulation Up regulation
In-vitro Model
LN-229 Glioblastoma Homo sapiens CVCL_0393
In-vivo Model Mice were randomly divided into control, sh-NC, and sh-RMRP groups by a researcher who was blinded to our experimental design. Each group contains 6 mice. U251/TMZ cells (1 × 107 cells/mouse), U251/TMZ cells infected with sh-NC (1 × 107 cells/mouse), or U251/TMZ cells infected with sh-RMRP (1 × 107 cells/mouse) were injected subcutaneously into the right-back of mice in the control, sh-NC, or sh-RMRP group, respectively. TMZ (25 mg/kg body weight) was intraperitoneally injected into mice every other day for 14 days when tumor volumes reached approximately 100 mm3.
Erythropoietin receptor (EPOR)
Acute myeloid leukaemia [ICD-11: 2A60]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [41]
Responsed Disease Acute myeloid leukaemia [ICD-11: 2A60]
Target Regulation Up regulation
In-vitro Model
KG-1a Adult acute myeloid leukemia Homo sapiens CVCL_1824
THP-1 Childhood acute monocytic leukemia Homo sapiens CVCL_0006
Fibronectin (FN1)
Renal cell carcinoma [ICD-11: 2C90]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [13]
Responsed Disease Renal cell carcinoma of kidney [ICD-11: 2C90.0]
Target Regulation Up regulation
Glutamate dehydrogenase 1, mitochondrial (GLUD1)
Cervical cancer [ICD-11: 2C77]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [23]
Responsed Disease Cervical cancer [ICD-11: 2C77]
Target Regulation Up regulation
Glutaminase kidney isoform, mitochondrial (GLS)
Gastric cancer [ICD-11: 2B72]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [42]
Responsed Disease Gastric cancer [ICD-11: 2B72]
Target Regulation Up regulation
In-vitro Model
GES-1 Normal Homo sapiens CVCL_EQ22
HGC-27 Gastric carcinoma Homo sapiens CVCL_1279
MKN28 Gastric tubular adenocarcinoma Homo sapiens CVCL_1416
MKN45 Gastric adenocarcinoma Homo sapiens CVCL_0434
AGS Gastric adenocarcinoma Homo sapiens CVCL_0139
SNU-1 Gastric adenocarcinoma Homo sapiens CVCL_0099
HEK293T Normal Homo sapiens CVCL_0063
Hexokinase-3 (HK3)
Renal cell carcinoma [ICD-11: 2C90]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [43]
Responsed Disease Renal cell carcinoma [ICD-11: 2C90]
Target Regulation Up regulation
In-vitro Model
A-498 Renal cell carcinoma Homo sapiens CVCL_1056
769-P Renal cell carcinoma Homo sapiens CVCL_1050
ACHN Papillary renal cell carcinoma Homo sapiens CVCL_1067
HK-2 [Human kidney] Normal Homo sapiens CVCL_0302
HEK293T Normal Homo sapiens CVCL_0063
THP-1 Childhood acute monocytic leukemia Homo sapiens CVCL_0006
In-vivo Model Xenograft mouse models were established by subcutaneously inoculating 1 × 107 transfected ACHN cells into mouse left flank.
Histone deacetylase 3 (HDAC3)
Acute ischemic stroke [ICD-11: 8B11]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [44]
Responsed Disease Acute ischemic stroke [ICD-11: 8B11]
Target Regulation Up regulation
Histone deacetylase 9 (HDAC9)
Acute laryngitis or tracheitis [ICD-11: CA05]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [45]
Responsed Disease Acute laryngitis or tracheitis [ICD-11: CA05]
In-vitro Model
TPC-1 Thyroid gland papillary carcinoma Homo sapiens CVCL_6298
B-CPAP Thyroid gland carcinoma Homo sapiens CVCL_0153
Histone-lysine N-methyltransferase SETMAR (SETMAR)
Thyroid Cancer [ICD-11: 2D10]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [46]
Responsed Disease Thyroid Cancer [ICD-11: 2D10]
Target Regulation Up regulation
Homeobox protein Hox-C10 (HOXC10)
Head and neck squamous carcinoma [ICD-11: 2B6E]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [47]
Responsed Disease Head and neck squamous carcinoma [ICD-11: 2B6E]
Target Regulation Up regulation
Pathway Response Wnt signaling pathway hsa04310
In-vitro Model
FaDu Hypopharyngeal squamous cell carcinoma Homo sapiens CVCL_1218
HuLa-PC
N.A. Homo sapiens CVCL_UC74
In-vivo Model Animals had free access to standard rodent chow and water. For the subcutaneous xenograft tumor model, transfected cells (5×106) were injected on the sides of the flanks of mice (n=5 per group). Subsequently, 30 days later, the mice were euthanized by cervical dislocation following anesthesia induced by intraperitoneal injection of 0.3% sodium pentobarbital (30 mg/kg). Euthanasia was confirmed by verifying respiratory and cardiac arrest, along with pupil dilation, for a minimum of 10 min. Tumor size and tumor weight were measured (max tumor diameter, 9.6 mm; max area, 82.56 mm2; max volume, 355.01 mm3). For the pulmonary metastasis model, transfected cells (2×106) were injected into the mouse tail veins (n=5 per group). Subsequently, 60 days later, the mice were sacrificed, and lungs were obtained. Finally, lung and tumor tissues were available for H&E staining at room temperature for 5 min or immunohistochemistry staining.
Hyaluronan synthase 2 (HAS2)
Breast cancer [ICD-11: 2C60]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [48]
Responsed Disease Breast cancer [ICD-11: 2C60]
Target Regulation Up regulation
In-vitro Model
MDA-MB-231 Breast adenocarcinoma Homo sapiens CVCL_0062
MDA-MB-157 Breast carcinoma Homo sapiens CVCL_0618
MCF-10A Normal Homo sapiens CVCL_0598
Hypoxia up-regulated protein 1 (HYOU1)
Breast cancer [ICD-11: 2C60]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [49]
Responsed Disease Breast cancer [ICD-11: 2C60]
Responsed Drug Doxil Approved
Target Regulation Up regulation
In-vitro Model
MCF-7 Invasive breast carcinoma Homo sapiens CVCL_0031
MDA-MB-231 Breast adenocarcinoma Homo sapiens CVCL_0062
JmjC domain-containing protein 8 (JMJD8)
Colorectal cancer [ICD-11: 2B91]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [50]
Responsed Disease Colorectal cancer [ICD-11: 2B91]
In-vitro Model
SW480 Colon adenocarcinoma Homo sapiens CVCL_0546
SW620 Colon adenocarcinoma Homo sapiens CVCL_0547
Laminin subunit alpha-5 (LAMA5)
Renal cell carcinoma [ICD-11: 2C90]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [13]
Responsed Disease Renal cell carcinoma of kidney [ICD-11: 2C90.0]
Target Regulation Up regulation
long intergenic non-protein coding RNA 632 (LINC00632)
Melanoma [ICD-11: 2C30]
In total 3 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [51]
Responsed Disease Melanoma [ICD-11: 2C30]
Responsed Drug ML-210 Investigative
Target Regulation Up regulation
In-vitro Model
451Lu Cutaneous melanoma Homo sapiens CVCL_6357
501-mel Melanoma Homo sapiens CVCL_4633
A-375 Amelanotic melanoma Homo sapiens CVCL_0132
SK-MEL-147 Melanoma Homo sapiens CVCL_3876
SK-MEL-173 Melanoma Homo sapiens CVCL_6090
SK-MEL-2 Melanoma Homo sapiens CVCL_0069
SK-MEL-239 Melanoma Homo sapiens CVCL_6122
SK-MEL-28 Cutaneous melanoma Homo sapiens CVCL_0526
WM115 Melanoma Homo sapiens CVCL_0040
WM1361A Cutaneous melanoma Homo sapiens CVCL_6788
WM1552C Cutaneous melanoma Homo sapiens CVCL_6472
WM266-4 Melanoma Homo sapiens CVCL_2765
WM278 Cutaneous melanoma Homo sapiens CVCL_6473
WM35 Melanoma Homo sapiens CVCL_0580
WM793b (Immunodeficient mice Cell Type melanocyte)
WM902B Melanoma Homo sapiens CVCL_6807
In-vivo Model 4-6 weeks old NOD/Shi-scid/IL-2Rgamma null (NOD.Cg-PrkdcscidIl2rgtm1Wjl/SzJ (NSG)) mice (female).
Response Summary CDR1 antisense RNA (CDR1-AS) a regulator of miR-7, as a hallmark of melanoma progression. CDR1as depletion results from epigenetic silencing of LINC00632, its originating long non-coding RNA (lncRNA) and promotes invasion in vitro and metastasis in vivo through a miR-7-independent, IGF2BP3-mediated mechanism. IGF2BP3 interacts with CDR1as and mediates invasion induced by CDR1as depletion. CDR1asHigh melanoma cell lines were strikingly more sensitive to three different GPX4 inhibitors, which are known to elicit ferroptotic cell death.
Experiment 2 Reporting the m6A-centered Disease Response of This Target Gene [51]
Responsed Disease Melanoma [ICD-11: 2C30]
Responsed Drug ML162 Investigative
Target Regulation Up regulation
In-vitro Model
451Lu Cutaneous melanoma Homo sapiens CVCL_6357
501-mel Melanoma Homo sapiens CVCL_4633
A-375 Amelanotic melanoma Homo sapiens CVCL_0132
SK-MEL-147 Melanoma Homo sapiens CVCL_3876
SK-MEL-173 Melanoma Homo sapiens CVCL_6090
SK-MEL-2 Melanoma Homo sapiens CVCL_0069
SK-MEL-239 Melanoma Homo sapiens CVCL_6122
SK-MEL-28 Cutaneous melanoma Homo sapiens CVCL_0526
WM115 Melanoma Homo sapiens CVCL_0040
WM1361A Cutaneous melanoma Homo sapiens CVCL_6788
WM1552C Cutaneous melanoma Homo sapiens CVCL_6472
WM266-4 Melanoma Homo sapiens CVCL_2765
WM278 Cutaneous melanoma Homo sapiens CVCL_6473
WM35 Melanoma Homo sapiens CVCL_0580
WM793b (Immunodeficient mice Cell Type melanocyte)
WM902B Melanoma Homo sapiens CVCL_6807
In-vivo Model 4-6 weeks old NOD/Shi-scid/IL-2Rgamma null (NOD.Cg-PrkdcscidIl2rgtm1Wjl/SzJ (NSG)) mice (female).
Response Summary CDR1 antisense RNA (CDR1-AS) a regulator of miR-7, as a hallmark of melanoma progression. CDR1as depletion results from epigenetic silencing of LINC00632, its originating long non-coding RNA (lncRNA) and promotes invasion in vitro and metastasis in vivo through a miR-7-independent, IGF2BP3-mediated mechanism. IGF2BP3 interacts with CDR1as and mediates invasion induced by CDR1as depletion. CDR1asHigh melanoma cell lines were strikingly more sensitive to three different GPX4 inhibitors, which are known to elicit ferroptotic cell death.
Experiment 3 Reporting the m6A-centered Disease Response of This Target Gene [51]
Responsed Disease Melanoma [ICD-11: 2C30]
Responsed Drug RSL3 Investigative
Target Regulation Up regulation
In-vitro Model
451Lu Cutaneous melanoma Homo sapiens CVCL_6357
501-mel Melanoma Homo sapiens CVCL_4633
A-375 Amelanotic melanoma Homo sapiens CVCL_0132
SK-MEL-147 Melanoma Homo sapiens CVCL_3876
SK-MEL-173 Melanoma Homo sapiens CVCL_6090
SK-MEL-2 Melanoma Homo sapiens CVCL_0069
SK-MEL-239 Melanoma Homo sapiens CVCL_6122
SK-MEL-28 Cutaneous melanoma Homo sapiens CVCL_0526
WM115 Melanoma Homo sapiens CVCL_0040
WM1361A Cutaneous melanoma Homo sapiens CVCL_6788
WM1552C Cutaneous melanoma Homo sapiens CVCL_6472
WM266-4 Melanoma Homo sapiens CVCL_2765
WM278 Cutaneous melanoma Homo sapiens CVCL_6473
WM35 Melanoma Homo sapiens CVCL_0580
WM793b (Immunodeficient mice Cell Type melanocyte)
WM902B Melanoma Homo sapiens CVCL_6807
In-vivo Model 4-6 weeks old NOD/Shi-scid/IL-2Rgamma null (NOD.Cg-PrkdcscidIl2rgtm1Wjl/SzJ (NSG)) mice (female).
Response Summary CDR1 antisense RNA (CDR1-AS) a regulator of miR-7, as a hallmark of melanoma progression. CDR1as depletion results from epigenetic silencing of LINC00632, its originating long non-coding RNA (lncRNA) and promotes invasion in vitro and metastasis in vivo through a miR-7-independent, IGF2BP3-mediated mechanism. IGF2BP3 interacts with CDR1as and mediates invasion induced by CDR1as depletion. CDR1asHigh melanoma cell lines were strikingly more sensitive to three different GPX4 inhibitors, which are known to elicit ferroptotic cell death.
Long intergenic non-protein coding RNA 662 (LINC00662)
Pancreatic cancer [ICD-11: 2C10]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [52]
Responsed Disease Pancreatic cancer [ICD-11: 2C10]
Target Regulation Up regulation
In-vitro Model
PANC-1 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0480
BxPC-3 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0186
MIA PaCa-2 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0428
COLO 357 Pancreatic adenosquamous carcinoma Homo sapiens CVCL_0221
CFPAC-1 Cystic fibrosis Homo sapiens CVCL_1119
Human Pancreatic Nestin-Expressing cells (Human Pancreatic Nestin-Expressing cells)
In-vivo Model For the tumor growth study, nude mice were subcutaneously inoculated into the flanks with PC cells (3 × 106) suspended in 0.1 mL PBS. Tumor volumes were calculated as 1/2 (length × width2) weekly. After 4 weeks, the xenograft tumors were harvested for analysis. To examine the role of the FAK inhibitor in tumor growth, nude mice were inoculated subcutaneously into the flanks with 3 × 106 stable cells suspended in 0.1 mL PBS. After 1 week, pre-established tumor xenografts were treated with Y15 (0.5 mg/kg, 2 ×/week × 3) (MCE, New Jersey, China). After another 3 weeks, the xenograft tumors were harvested for analysis. In the metastasis model, PC cells (2 × 106) in 0.1 mL PBS were injected into nude mice through their tail veins. Six weeks later, the lungs were removed for the evaluation of lung metastasis using hematoxylin and eosin (H&E) staining.
M-phase inducer phosphatase 1 (CDC25A)
Malignant neoplasms of oesophagogastric junction [ICD-11: 2B71]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [53]
Responsed Disease Malignant neoplasms of oesophagogastric junction [ICD-11: 2B71.0]
In-vitro Model
OE19 Esophageal adenocarcinoma Homo sapiens CVCL_1622
N-myc proto-oncogene protein (MYCN)
Brain cancer [ICD-11: 2A00]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [54]
Responsed Disease Neuroblastoma [ICD-11: 2A00.11]
Target Regulation Up regulation
In-vitro Model
SK-N-BE(2) Neuroblastoma Homo sapiens CVCL_0528
IMR-32 Neuroblastoma Homo sapiens CVCL_0346
SK-N-BE(2) Neuroblastoma Homo sapiens CVCL_0528
SK-N-SH Neuroblastoma Homo sapiens CVCL_0531
SH-SY5Y Neuroblastoma Homo sapiens CVCL_0019
In-vivo Model Male 5-week-old BALB/c-nu mice were provided by Shanghai SLAC Laboratory Animal CO. LTD. Cells (5 × 106 cells suspended in 0.1 mL PBS) were injected subcutaneously from the axilla of each nude mouse. After 12 days, the long (L) and short (S) diameters of the tumors were measured with vernier caliper every 3 days (0.5 × L × S2). The growth curve of subcutaneous tumors was drawn on the basis of the measured tumor volume. The experimental subjects were killed 33 days after the injection of cells, and subcutaneous tumors were removed completely.
Neurofibromin (NF1)
Triple-negative breast cancer [ICD-11: 2C6Z]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [55]
Responsed Disease Triple-negative breast cancer [ICD-11: 2C6Z]
Target Regulation Down regulation
In-vitro Model
MCF-7 Invasive breast carcinoma Homo sapiens CVCL_0031
BT-474 Invasive breast carcinoma Homo sapiens CVCL_0179
ZR-75-1 Invasive breast carcinoma Homo sapiens CVCL_0588
SK-BR-3 Breast adenocarcinoma Homo sapiens CVCL_0033
MDA-MB-453 Breast adenocarcinoma Homo sapiens CVCL_0418
HCC1806 Breast squamous cell carcinoma Homo sapiens CVCL_1258
MDA-MB-231 Breast adenocarcinoma Homo sapiens CVCL_0062
BT-549 Invasive breast carcinoma Homo sapiens CVCL_1092
In-vivo Model BALB/c nude mice (4-6 weeks) were randomly divided into four groups. Stable shRNA-NC, shIGF2BP3, shRNA-NC + siNF1 and shIGF2BP3 + siNF1 MDA-MB-231 cells were injected into each group of mice (1 × 107 cells/mouse). In addition, tumour volumes were recorded every 4 days.
Pirin (PIR)
Melanoma of uvea [ICD-11: 2D0Y]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [56]
Responsed Disease Melanoma of uvea [ICD-11: 2D0Y]
Target Regulation Up regulation
Protein diaphanous homolog 3 (DIAPH3)
Liver cancer [ICD-11: 2C12]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [57]
Responsed Disease Liver cancer [ICD-11: 2C12]
Target Regulation Up regulation
In-vitro Model
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
SK-HEP-1 Liver and intrahepatic bile duct epithelial neoplasm Homo sapiens CVCL_0525
Huh-7 Adult hepatocellular carcinoma Homo sapiens CVCL_0336
SNU-387 Adult hepatocellular carcinoma Homo sapiens CVCL_0250
SNU-182 Adult hepatocellular carcinoma Homo sapiens CVCL_0090
HEK293 Normal Homo sapiens CVCL_0045
In-vivo Model A total of 5×106 SK-Hep-1 cells (shNC, sh1089-1, or sh1089-2) into fossa axillaries of 5-week-old male nude BALB/c mice (Vital River Laboratory; n = 5 per group).in vivo, we injected a total of 2×107 SK-Hep-1 cells with stable LINC01089-KD (shNC, sh1089-1, or sh1089-2) or LINC01089-OE (NC or lnc1089) into the middle of the lower abdomen of male nude BALB/c mice (Vital River Laboratory; n = 6 per group).To investigate the involvement of LINC01089 in hematogenous metastases, a total of 1×107 SK-Hep-1 cells with stable firefly luciferase expression (shNC, sh1089-1, sh1089-2, NC, or lnc1089) were injected into tail vein of male nude BALB/c mice (Vital River Laboratory; n = 4 per group).
Semaphorin-3F (SEMA3F)
Prostate cancer [ICD-11: 2C82]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [58]
Responsed Disease Prostate cancer [ICD-11: 2C82]
In-vitro Model
RWPE-1 Normal Homo sapiens CVCL_3791
DU145 Prostate carcinoma Homo sapiens CVCL_0105
PC-3 Prostate carcinoma Homo sapiens CVCL_0035
22Rv1 Prostate carcinoma Homo sapiens CVCL_1045
LNCaP Prostate carcinoma Homo sapiens CVCL_0395
LNCaP C4-2B Prostate carcinoma Homo sapiens CVCL_4784
VCaP Prostate carcinoma Homo sapiens CVCL_2235
HEK293T Normal Homo sapiens CVCL_0063
In-vivo Model All the animal studies and protocols followed the institutional guidelines of the First Affiliated Hospital, School of Medicine, Zhejiang University.
Translation machinery-associated protein 7 (TMA7)
Laryngeal cancer [ICD-11: 2C23]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [59]
Responsed Disease Laryngeal cancer [ICD-11: 2C23]
Responsed Drug Cisplatin Approved
Target Regulation Up regulation
In-vitro Model
Tu 212 Head and neck squamous cell carcinoma Homo sapiens CVCL_4915
Tu 177 Laryngeal squamous cell carcinoma Homo sapiens CVCL_4913
AMC-HN-8 Laryngeal squamous cell carcinoma Homo sapiens CVCL_5966
In-vivo Model Male BALB/c nude mice (4-weeks-old; body weight 20-25 g; n=15) were obtained from Vital River Laboratories (Beijing, China) and maintained at 20-26 °C and 40-70% humidity with specific pathogen-free conditions. The mice were divided into control, TMA7 KD, and TMA7 KD+UBA2 OE groups. Each nude mouse was injected with 100 μL (1.0x107 cells) of lentivirus-transfected LSCC cells. The formula length×width 2×0.5 was used to calculate the tumor volume. 34 days after inoculation, the xenografts were excised, and their volume was determined.
Trinucleotide repeat-containing gene 6A protein (TNRC6A)
Renal cell carcinoma [ICD-11: 2C90]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [11]
Responsed Disease Renal cell carcinoma [ICD-11: 2C90]
Responsed Drug Sunitinib Approved
In-vitro Model
ACHN Papillary renal cell carcinoma Homo sapiens CVCL_1067
A-498 Renal cell carcinoma Homo sapiens CVCL_1056
Caki-1 Clear cell renal cell carcinoma Homo sapiens CVCL_0234
OS-RC-2 Clear cell renal cell carcinoma Homo sapiens CVCL_1626
786-O Renal cell carcinoma Homo sapiens CVCL_1051
HK-2 [Human kidney] Normal Homo sapiens CVCL_0302
In-vivo Model A total of 1 × 106 ACHN cells was injected into left renal capsule (n = 5 mice/group). Then, we sutured the wound layer by layer. Tumour size was measured 4 weeks later with in-Vivo FX PRO small animal imaging system (BRUKER). After that, we executed the mice and collected tumours for immunohistochemistry (IHC) assays and Western blotting. For metastasis model construction, 1 × 106 ACHN cells were injected into tail-vein of each mouse (n = 5 mice/group).
Zinc finger MIZ domain-containing protein 2 (ZMIZ2)
Renal cell carcinoma [ICD-11: 2C90]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [11]
Responsed Disease Renal cell carcinoma [ICD-11: 2C90]
Responsed Drug Sunitinib Approved
In-vitro Model
ACHN Papillary renal cell carcinoma Homo sapiens CVCL_1067
A-498 Renal cell carcinoma Homo sapiens CVCL_1056
Caki-1 Clear cell renal cell carcinoma Homo sapiens CVCL_0234
OS-RC-2 Clear cell renal cell carcinoma Homo sapiens CVCL_1626
786-O Renal cell carcinoma Homo sapiens CVCL_1051
HK-2 [Human kidney] Normal Homo sapiens CVCL_0302
In-vivo Model A total of 1 × 106 ACHN cells was injected into left renal capsule (n = 5 mice/group). Then, we sutured the wound layer by layer. Tumour size was measured 4 weeks later with in-Vivo FX PRO small animal imaging system (BRUKER). After that, we executed the mice and collected tumours for immunohistochemistry (IHC) assays and Western blotting. For metastasis model construction, 1 × 106 ACHN cells were injected into tail-vein of each mouse (n = 5 mice/group).
Unspecific Target Gene
Pancreatic cancer [ICD-11: 2C10]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [60]
Responsed Disease Pancreatic cancer [ICD-11: 2C10]
Responsed Drug Gemcitabine Approved
Pathway Response Adipocytokine signaling pathway hsa04920
Cell Process Epithelial-mesenchymal transition
In-vitro Model
BxPC-3 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0186
HDE-CT cell line (A normal human pancreatic cell line)
MIA PaCa-2 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0428
Response Summary Lasso regression identified a six-m6A-regulator-signature prognostic model (KIAA1429, HNRNPC, METTL3, YTHDF1, IGF2BP2, and IGF2BP3). Gene set enrichment analysis revealed m6A regulators (KIAA1429, HNRNPC, and IGF2BP2) were related to multiple biological behaviors in pancreatic cancer, including adipocytokine signaling, the well vs. poorly differentiated tumor pathway, tumor metastasis pathway, epithelial mesenchymal transition pathway, gemcitabine resistance pathway, and stemness pathway.
Lung cancer [ICD-11: 2C25]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [61]
Responsed Disease Lung adenocarcinoma [ICD-11: 2C25.0]
Response Summary IGF2BP3 is an oncogene and potential prognostic biomarker of LUAD.
Breast cancer [ICD-11: 2C60]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [62]
Responsed Disease Breast cancer [ICD-11: 2C60]
Osteoarthritis [ICD-11: FA05]
In total 1 item(s) under this disease
Experiment 1 Reporting the m6A-centered Disease Response of This Target Gene [63]
Responsed Disease Osteoarthritis [ICD-11: FA05]
ATP-dependent translocase ABCB1 (ABCB1)
Representative RNA-seq result indicating the expression of this target gene regulated by IGF2BP3
Cell Line ES-2 cell line Homo sapiens
Treatment: siIGF2BP3 ES-2 cells
Control: siControl ES-2 cells
GSE109604
Regulation
logFC: -1.30E+00
p-value: 4.65E-03
More Results Click to View More RNA-seq Results
Doxil [Approved]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [1]
Responsed Disease Colorectal cancer ICD-11: 2B91
Target Regulation Up regulation
Pathway Response ABC transporters hsa02010
Cell Process RNA stability
In-vitro Model DLD-1 Colon adenocarcinoma Homo sapiens CVCL_0248
HCT 116 Colon carcinoma Homo sapiens CVCL_0291
HCT 15 Colon adenocarcinoma Homo sapiens CVCL_0292
HCT 8 Colon adenocarcinoma Homo sapiens CVCL_2478
HT29 Colon cancer Mus musculus CVCL_A8EZ
SW1463 Rectal adenocarcinoma Homo sapiens CVCL_1718
SW480 Colon adenocarcinoma Homo sapiens CVCL_0546
SW620 Colon adenocarcinoma Homo sapiens CVCL_0547
In-vivo Model HCT8/T xenografts derived from shNC or shIGF2BP3-1 HCT8/T cells were established through subcutaneous inoculation of cells (6×106) into nude mice.
Response Summary IGF2BP3, directly bound to the m6A-modified region of ATP-dependent translocase ABCB1 (ABCB1) mRNA, thereby promoting the stability and expression of ABCB1 mRNA. The expression of IGF2BP3 and ABCB1 was strongly correlated with DOX sensitivity. Targeting IGF2BP3 was an important chemotherapeutic strategy for preventing MDR development in colorectal cancer.
Autophagy protein 5 (ATG5)
Spautin 1 [Preclinical]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [9]
Responsed Disease Osteosarcoma ICD-11: 2B51
Target Regulation Up regulation
In-vivo Model For tumor growth assay, 2 × 106 OS cells in 100 μL medium were injected into the nude mice subcutaneously. For tumor metastasis assay, we injected medium containing 2 × 106 cells through the caudal vein. An IVIS200 imaging system (Caliper Life Science, USA) was used to image and assess the OS metastasis. For pharmacological inhibition of USP13, mice bearing xenografts were treated with Spautin-1 (40 mg/kg/day i.p.) or vehicle for 2 weeks.
CD44 antigen (CD44)
Sunitinib [Approved]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [11]
Responsed Disease Renal cell carcinoma ICD-11: 2C90
In-vitro Model ACHN Papillary renal cell carcinoma Homo sapiens CVCL_1067
A-498 Renal cell carcinoma Homo sapiens CVCL_1056
Caki-1 Clear cell renal cell carcinoma Homo sapiens CVCL_0234
OS-RC-2 Clear cell renal cell carcinoma Homo sapiens CVCL_1626
786-O Renal cell carcinoma Homo sapiens CVCL_1051
HK-2 [Human kidney] Normal Homo sapiens CVCL_0302
In-vivo Model A total of 1 × 106 ACHN cells was injected into left renal capsule (n = 5 mice/group). Then, we sutured the wound layer by layer. Tumour size was measured 4 weeks later with in-Vivo FX PRO small animal imaging system (BRUKER). After that, we executed the mice and collected tumours for immunohistochemistry (IHC) assays and Western blotting. For metastasis model construction, 1 × 106 ACHN cells were injected into tail-vein of each mouse (n = 5 mice/group).
High mobility group protein HMGI-C (HMGA2)
Sunitinib [Approved]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [11]
Responsed Disease Renal cell carcinoma ICD-11: 2C90
In-vitro Model ACHN Papillary renal cell carcinoma Homo sapiens CVCL_1067
A-498 Renal cell carcinoma Homo sapiens CVCL_1056
Caki-1 Clear cell renal cell carcinoma Homo sapiens CVCL_0234
OS-RC-2 Clear cell renal cell carcinoma Homo sapiens CVCL_1626
786-O Renal cell carcinoma Homo sapiens CVCL_1051
HK-2 [Human kidney] Normal Homo sapiens CVCL_0302
In-vivo Model A total of 1 × 106 ACHN cells was injected into left renal capsule (n = 5 mice/group). Then, we sutured the wound layer by layer. Tumour size was measured 4 weeks later with in-Vivo FX PRO small animal imaging system (BRUKER). After that, we executed the mice and collected tumours for immunohistochemistry (IHC) assays and Western blotting. For metastasis model construction, 1 × 106 ACHN cells were injected into tail-vein of each mouse (n = 5 mice/group).
Myc proto-oncogene protein (MYC)
Linsitinib [Phase 3]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [24]
Responsed Disease Glioma ICD-11: 2A00.0
Target Regulation Up regulation
Pathway Response RNA degradation hsa03018
Cell Process RNA stability
In-vitro Model ()
HNP1 (A human neural progenitor cell)
NHA (Normal human astrocytes)
NSC11 (Pluripotent derived neural progenitor cell)
In-vivo Model For in vivo drug treatment studies, intracranial xenografts were generated by implanting 5000 patient-derived GSCs (387 and 4121) into the right cerebral cortex of NSG mice as described above.
Response Summary The m6A reader YTHDF2 stabilized Myc proto-oncogene protein (MYC) mRNA specifically in cancer stem cells. Given the challenge of targeting MYC, YTHDF2 presents a therapeutic target to perturb MYC signaling in glioblastoma. The IGF1/IGF1R inhibitor linsitinib preferentially targeted YTHDF2-expressing cells, inhibiting GSC viability without affecting NSCs and impairing in vivo glioblastoma growth. YTHDF2 links RNA epitranscriptomic modifications and GSC growth, laying the foundation for the YTHDF2-MYC-IGFBP3 axis as a specific and novel therapeutic target in glioblastoma.
Calpain-15 (CAPN15)
Sunitinib [Approved]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [11]
Responsed Disease Renal cell carcinoma ICD-11: 2C90
In-vitro Model ACHN Papillary renal cell carcinoma Homo sapiens CVCL_1067
A-498 Renal cell carcinoma Homo sapiens CVCL_1056
Caki-1 Clear cell renal cell carcinoma Homo sapiens CVCL_0234
OS-RC-2 Clear cell renal cell carcinoma Homo sapiens CVCL_1626
786-O Renal cell carcinoma Homo sapiens CVCL_1051
HK-2 [Human kidney] Normal Homo sapiens CVCL_0302
In-vivo Model A total of 1 × 106 ACHN cells was injected into left renal capsule (n = 5 mice/group). Then, we sutured the wound layer by layer. Tumour size was measured 4 weeks later with in-Vivo FX PRO small animal imaging system (BRUKER). After that, we executed the mice and collected tumours for immunohistochemistry (IHC) assays and Western blotting. For metastasis model construction, 1 × 106 ACHN cells were injected into tail-vein of each mouse (n = 5 mice/group).
Cullin-1 (CUL1)
Etoposide [Approved]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [38]
Target Regulation Down regulation
Pathway Response Wnt signaling pathway hsa04310
In-vitro Model BEAS-2B Normal Homo sapiens CVCL_0168
NCI-H1299 Lung large cell carcinoma Homo sapiens CVCL_0060
NCI-H1975 Lung adenocarcinoma Homo sapiens CVCL_1511
A-549 Lung adenocarcinoma Homo sapiens CVCL_0023
PC-9 Lung adenocarcinoma Homo sapiens CVCL_B260
BEL-7404 Endocervical adenocarcinoma Homo sapiens CVCL_6568
BEL-7402 Endocervical adenocarcinoma Homo sapiens CVCL_5492
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
SW1990 Pancreatic adenocarcinoma Homo sapiens CVCL_1723
PANC-1 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0480
MKN45 Gastric adenocarcinoma Homo sapiens CVCL_0434
MGC-803 Gastric mucinous adenocarcinoma Homo sapiens CVCL_5334
HCT 116 Colon carcinoma Homo sapiens CVCL_0291
HT29 Colon cancer Mus musculus CVCL_A8EZ
In-vivo Model For the generation of PDX mouse models, fresh LUSC specimens (2-3 mm3), which were from Shanghai Chest Hospital, were implanted into 4- to 6-week-old athymic nude mice (Jiesijie, Shanghai, China). After successful tumor growth was confirmed, the tumor tissues were passaged and implanted into the next generation of mice. The third to fifth generations of PDX-bearing mice were used for drug administration. When tumors reached approximately 200 mm3, mice were injected daily with DMSO (no. ST038, Beyotime Biotechnology, Shanghai, China) with or without MIT (no. S2485, 5 mg/kg, Selleck, Houston, TX) or HYD (no. S1896, 20 mg/kg, Selleck) (n = 5 mice/group). Tumor growth was monitored, and sizes were calculated by 0.5 × L × W2 (L indicating length and W indicating width). The mice were euthanized at day 28 after implantation. All animal experiments were approved by the institutional ethics committee of Shanghai Chest Hospital (approval number KS(Y)21383).
Hydroxyurea [Approved]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [38]
Target Regulation Down regulation
Pathway Response Wnt signaling pathway hsa04310
In-vitro Model BEAS-2B Normal Homo sapiens CVCL_0168
NCI-H1299 Lung large cell carcinoma Homo sapiens CVCL_0060
NCI-H1975 Lung adenocarcinoma Homo sapiens CVCL_1511
A-549 Lung adenocarcinoma Homo sapiens CVCL_0023
PC-9 Lung adenocarcinoma Homo sapiens CVCL_B260
BEL-7404 Endocervical adenocarcinoma Homo sapiens CVCL_6568
BEL-7402 Endocervical adenocarcinoma Homo sapiens CVCL_5492
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
SW1990 Pancreatic adenocarcinoma Homo sapiens CVCL_1723
PANC-1 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0480
MKN45 Gastric adenocarcinoma Homo sapiens CVCL_0434
MGC-803 Gastric mucinous adenocarcinoma Homo sapiens CVCL_5334
HCT 116 Colon carcinoma Homo sapiens CVCL_0291
HT29 Colon cancer Mus musculus CVCL_A8EZ
In-vivo Model For the generation of PDX mouse models, fresh LUSC specimens (2-3 mm3), which were from Shanghai Chest Hospital, were implanted into 4- to 6-week-old athymic nude mice (Jiesijie, Shanghai, China). After successful tumor growth was confirmed, the tumor tissues were passaged and implanted into the next generation of mice. The third to fifth generations of PDX-bearing mice were used for drug administration. When tumors reached approximately 200 mm3, mice were injected daily with DMSO (no. ST038, Beyotime Biotechnology, Shanghai, China) with or without MIT (no. S2485, 5 mg/kg, Selleck, Houston, TX) or HYD (no. S1896, 20 mg/kg, Selleck) (n = 5 mice/group). Tumor growth was monitored, and sizes were calculated by 0.5 × L × W2 (L indicating length and W indicating width). The mice were euthanized at day 28 after implantation. All animal experiments were approved by the institutional ethics committee of Shanghai Chest Hospital (approval number KS(Y)21383).
Mitoxantrone [Approved]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [38]
Target Regulation Down regulation
Pathway Response Wnt signaling pathway hsa04310
In-vitro Model BEAS-2B Normal Homo sapiens CVCL_0168
NCI-H1299 Lung large cell carcinoma Homo sapiens CVCL_0060
NCI-H1975 Lung adenocarcinoma Homo sapiens CVCL_1511
A-549 Lung adenocarcinoma Homo sapiens CVCL_0023
PC-9 Lung adenocarcinoma Homo sapiens CVCL_B260
BEL-7404 Endocervical adenocarcinoma Homo sapiens CVCL_6568
BEL-7402 Endocervical adenocarcinoma Homo sapiens CVCL_5492
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
SW1990 Pancreatic adenocarcinoma Homo sapiens CVCL_1723
PANC-1 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0480
MKN45 Gastric adenocarcinoma Homo sapiens CVCL_0434
MGC-803 Gastric mucinous adenocarcinoma Homo sapiens CVCL_5334
HCT 116 Colon carcinoma Homo sapiens CVCL_0291
HT29 Colon cancer Mus musculus CVCL_A8EZ
In-vivo Model For the generation of PDX mouse models, fresh LUSC specimens (2-3 mm3), which were from Shanghai Chest Hospital, were implanted into 4- to 6-week-old athymic nude mice (Jiesijie, Shanghai, China). After successful tumor growth was confirmed, the tumor tissues were passaged and implanted into the next generation of mice. The third to fifth generations of PDX-bearing mice were used for drug administration. When tumors reached approximately 200 mm3, mice were injected daily with DMSO (no. ST038, Beyotime Biotechnology, Shanghai, China) with or without MIT (no. S2485, 5 mg/kg, Selleck, Houston, TX) or HYD (no. S1896, 20 mg/kg, Selleck) (n = 5 mice/group). Tumor growth was monitored, and sizes were calculated by 0.5 × L × W2 (L indicating length and W indicating width). The mice were euthanized at day 28 after implantation. All animal experiments were approved by the institutional ethics committee of Shanghai Chest Hospital (approval number KS(Y)21383).
Oxaliplatin [Approved]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [38]
Target Regulation Down regulation
Pathway Response Wnt signaling pathway hsa04310
In-vitro Model BEAS-2B Normal Homo sapiens CVCL_0168
NCI-H1299 Lung large cell carcinoma Homo sapiens CVCL_0060
NCI-H1975 Lung adenocarcinoma Homo sapiens CVCL_1511
A-549 Lung adenocarcinoma Homo sapiens CVCL_0023
PC-9 Lung adenocarcinoma Homo sapiens CVCL_B260
BEL-7404 Endocervical adenocarcinoma Homo sapiens CVCL_6568
BEL-7402 Endocervical adenocarcinoma Homo sapiens CVCL_5492
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
SW1990 Pancreatic adenocarcinoma Homo sapiens CVCL_1723
PANC-1 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0480
MKN45 Gastric adenocarcinoma Homo sapiens CVCL_0434
MGC-803 Gastric mucinous adenocarcinoma Homo sapiens CVCL_5334
HCT 116 Colon carcinoma Homo sapiens CVCL_0291
HT29 Colon cancer Mus musculus CVCL_A8EZ
In-vivo Model For the generation of PDX mouse models, fresh LUSC specimens (2-3 mm3), which were from Shanghai Chest Hospital, were implanted into 4- to 6-week-old athymic nude mice (Jiesijie, Shanghai, China). After successful tumor growth was confirmed, the tumor tissues were passaged and implanted into the next generation of mice. The third to fifth generations of PDX-bearing mice were used for drug administration. When tumors reached approximately 200 mm3, mice were injected daily with DMSO (no. ST038, Beyotime Biotechnology, Shanghai, China) with or without MIT (no. S2485, 5 mg/kg, Selleck, Houston, TX) or HYD (no. S1896, 20 mg/kg, Selleck) (n = 5 mice/group). Tumor growth was monitored, and sizes were calculated by 0.5 × L × W2 (L indicating length and W indicating width). The mice were euthanized at day 28 after implantation. All animal experiments were approved by the institutional ethics committee of Shanghai Chest Hospital (approval number KS(Y)21383).
Raltitrexed [Approved]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [38]
Target Regulation Down regulation
Pathway Response Wnt signaling pathway hsa04310
In-vitro Model BEAS-2B Normal Homo sapiens CVCL_0168
NCI-H1299 Lung large cell carcinoma Homo sapiens CVCL_0060
NCI-H1975 Lung adenocarcinoma Homo sapiens CVCL_1511
A-549 Lung adenocarcinoma Homo sapiens CVCL_0023
PC-9 Lung adenocarcinoma Homo sapiens CVCL_B260
BEL-7404 Endocervical adenocarcinoma Homo sapiens CVCL_6568
BEL-7402 Endocervical adenocarcinoma Homo sapiens CVCL_5492
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
SW1990 Pancreatic adenocarcinoma Homo sapiens CVCL_1723
PANC-1 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0480
MKN45 Gastric adenocarcinoma Homo sapiens CVCL_0434
MGC-803 Gastric mucinous adenocarcinoma Homo sapiens CVCL_5334
HCT 116 Colon carcinoma Homo sapiens CVCL_0291
HT29 Colon cancer Mus musculus CVCL_A8EZ
In-vivo Model For the generation of PDX mouse models, fresh LUSC specimens (2-3 mm3), which were from Shanghai Chest Hospital, were implanted into 4- to 6-week-old athymic nude mice (Jiesijie, Shanghai, China). After successful tumor growth was confirmed, the tumor tissues were passaged and implanted into the next generation of mice. The third to fifth generations of PDX-bearing mice were used for drug administration. When tumors reached approximately 200 mm3, mice were injected daily with DMSO (no. ST038, Beyotime Biotechnology, Shanghai, China) with or without MIT (no. S2485, 5 mg/kg, Selleck, Houston, TX) or HYD (no. S1896, 20 mg/kg, Selleck) (n = 5 mice/group). Tumor growth was monitored, and sizes were calculated by 0.5 × L × W2 (L indicating length and W indicating width). The mice were euthanized at day 28 after implantation. All animal experiments were approved by the institutional ethics committee of Shanghai Chest Hospital (approval number KS(Y)21383).
E3 ubiquitin-protein ligase ZNRF3 (ZNRF3)
Temozolomide [Approved]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [40]
Responsed Disease Brain cancer ICD-11: 2A00
Target Regulation Up regulation
In-vitro Model LN-229 Glioblastoma Homo sapiens CVCL_0393
In-vivo Model Mice were randomly divided into control, sh-NC, and sh-RMRP groups by a researcher who was blinded to our experimental design. Each group contains 6 mice. U251/TMZ cells (1 × 107 cells/mouse), U251/TMZ cells infected with sh-NC (1 × 107 cells/mouse), or U251/TMZ cells infected with sh-RMRP (1 × 107 cells/mouse) were injected subcutaneously into the right-back of mice in the control, sh-NC, or sh-RMRP group, respectively. TMZ (25 mg/kg body weight) was intraperitoneally injected into mice every other day for 14 days when tumor volumes reached approximately 100 mm3.
Hypoxia up-regulated protein 1 (HYOU1)
Doxil [Approved]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [49]
Responsed Disease Breast cancer ICD-11: 2C60
Target Regulation Up regulation
In-vitro Model MCF-7 Invasive breast carcinoma Homo sapiens CVCL_0031
MDA-MB-231 Breast adenocarcinoma Homo sapiens CVCL_0062
long intergenic non-protein coding RNA 632 (LINC00632)
ML-210 [Investigative]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [51]
Responsed Disease Melanoma ICD-11: 2C30
Target Regulation Up regulation
In-vitro Model 451Lu Cutaneous melanoma Homo sapiens CVCL_6357
501-mel Melanoma Homo sapiens CVCL_4633
A-375 Amelanotic melanoma Homo sapiens CVCL_0132
SK-MEL-147 Melanoma Homo sapiens CVCL_3876
SK-MEL-173 Melanoma Homo sapiens CVCL_6090
SK-MEL-2 Melanoma Homo sapiens CVCL_0069
SK-MEL-239 Melanoma Homo sapiens CVCL_6122
SK-MEL-28 Cutaneous melanoma Homo sapiens CVCL_0526
WM115 Melanoma Homo sapiens CVCL_0040
WM1361A Cutaneous melanoma Homo sapiens CVCL_6788
WM1552C Cutaneous melanoma Homo sapiens CVCL_6472
WM266-4 Melanoma Homo sapiens CVCL_2765
WM278 Cutaneous melanoma Homo sapiens CVCL_6473
WM35 Melanoma Homo sapiens CVCL_0580
WM793b (Immunodeficient mice Cell Type melanocyte)
WM902B Melanoma Homo sapiens CVCL_6807
In-vivo Model 4-6 weeks old NOD/Shi-scid/IL-2Rgamma null (NOD.Cg-PrkdcscidIl2rgtm1Wjl/SzJ (NSG)) mice (female).
Response Summary CDR1 antisense RNA (CDR1-AS) a regulator of miR-7, as a hallmark of melanoma progression. CDR1as depletion results from epigenetic silencing of LINC00632, its originating long non-coding RNA (lncRNA) and promotes invasion in vitro and metastasis in vivo through a miR-7-independent, IGF2BP3-mediated mechanism. IGF2BP3 interacts with CDR1as and mediates invasion induced by CDR1as depletion. CDR1asHigh melanoma cell lines were strikingly more sensitive to three different GPX4 inhibitors, which are known to elicit ferroptotic cell death.
ML162 [Investigative]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [51]
Responsed Disease Melanoma ICD-11: 2C30
Target Regulation Up regulation
In-vitro Model 451Lu Cutaneous melanoma Homo sapiens CVCL_6357
501-mel Melanoma Homo sapiens CVCL_4633
A-375 Amelanotic melanoma Homo sapiens CVCL_0132
SK-MEL-147 Melanoma Homo sapiens CVCL_3876
SK-MEL-173 Melanoma Homo sapiens CVCL_6090
SK-MEL-2 Melanoma Homo sapiens CVCL_0069
SK-MEL-239 Melanoma Homo sapiens CVCL_6122
SK-MEL-28 Cutaneous melanoma Homo sapiens CVCL_0526
WM115 Melanoma Homo sapiens CVCL_0040
WM1361A Cutaneous melanoma Homo sapiens CVCL_6788
WM1552C Cutaneous melanoma Homo sapiens CVCL_6472
WM266-4 Melanoma Homo sapiens CVCL_2765
WM278 Cutaneous melanoma Homo sapiens CVCL_6473
WM35 Melanoma Homo sapiens CVCL_0580
WM793b (Immunodeficient mice Cell Type melanocyte)
WM902B Melanoma Homo sapiens CVCL_6807
In-vivo Model 4-6 weeks old NOD/Shi-scid/IL-2Rgamma null (NOD.Cg-PrkdcscidIl2rgtm1Wjl/SzJ (NSG)) mice (female).
Response Summary CDR1 antisense RNA (CDR1-AS) a regulator of miR-7, as a hallmark of melanoma progression. CDR1as depletion results from epigenetic silencing of LINC00632, its originating long non-coding RNA (lncRNA) and promotes invasion in vitro and metastasis in vivo through a miR-7-independent, IGF2BP3-mediated mechanism. IGF2BP3 interacts with CDR1as and mediates invasion induced by CDR1as depletion. CDR1asHigh melanoma cell lines were strikingly more sensitive to three different GPX4 inhibitors, which are known to elicit ferroptotic cell death.
RSL3 [Investigative]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [51]
Responsed Disease Melanoma ICD-11: 2C30
Target Regulation Up regulation
In-vitro Model 451Lu Cutaneous melanoma Homo sapiens CVCL_6357
501-mel Melanoma Homo sapiens CVCL_4633
A-375 Amelanotic melanoma Homo sapiens CVCL_0132
SK-MEL-147 Melanoma Homo sapiens CVCL_3876
SK-MEL-173 Melanoma Homo sapiens CVCL_6090
SK-MEL-2 Melanoma Homo sapiens CVCL_0069
SK-MEL-239 Melanoma Homo sapiens CVCL_6122
SK-MEL-28 Cutaneous melanoma Homo sapiens CVCL_0526
WM115 Melanoma Homo sapiens CVCL_0040
WM1361A Cutaneous melanoma Homo sapiens CVCL_6788
WM1552C Cutaneous melanoma Homo sapiens CVCL_6472
WM266-4 Melanoma Homo sapiens CVCL_2765
WM278 Cutaneous melanoma Homo sapiens CVCL_6473
WM35 Melanoma Homo sapiens CVCL_0580
WM793b (Immunodeficient mice Cell Type melanocyte)
WM902B Melanoma Homo sapiens CVCL_6807
In-vivo Model 4-6 weeks old NOD/Shi-scid/IL-2Rgamma null (NOD.Cg-PrkdcscidIl2rgtm1Wjl/SzJ (NSG)) mice (female).
Response Summary CDR1 antisense RNA (CDR1-AS) a regulator of miR-7, as a hallmark of melanoma progression. CDR1as depletion results from epigenetic silencing of LINC00632, its originating long non-coding RNA (lncRNA) and promotes invasion in vitro and metastasis in vivo through a miR-7-independent, IGF2BP3-mediated mechanism. IGF2BP3 interacts with CDR1as and mediates invasion induced by CDR1as depletion. CDR1asHigh melanoma cell lines were strikingly more sensitive to three different GPX4 inhibitors, which are known to elicit ferroptotic cell death.
RNA component of 7SK nuclear ribonucleoprotein (RN7SK)
Etoposide [Approved]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [38]
Target Regulation Up regulation
Pathway Response Wnt signaling pathway hsa04310
In-vitro Model BEAS-2B Normal Homo sapiens CVCL_0168
NCI-H1299 Lung large cell carcinoma Homo sapiens CVCL_0060
NCI-H1975 Lung adenocarcinoma Homo sapiens CVCL_1511
A-549 Lung adenocarcinoma Homo sapiens CVCL_0023
PC-9 Lung adenocarcinoma Homo sapiens CVCL_B260
BEL-7404 Endocervical adenocarcinoma Homo sapiens CVCL_6568
BEL-7402 Endocervical adenocarcinoma Homo sapiens CVCL_5492
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
SW1990 Pancreatic adenocarcinoma Homo sapiens CVCL_1723
PANC-1 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0480
MKN45 Gastric adenocarcinoma Homo sapiens CVCL_0434
MGC-803 Gastric mucinous adenocarcinoma Homo sapiens CVCL_5334
HCT 116 Colon carcinoma Homo sapiens CVCL_0291
HT29 Colon cancer Mus musculus CVCL_A8EZ
MCF-7 Invasive breast carcinoma Homo sapiens CVCL_0031
In-vivo Model For the generation of PDX mouse models, fresh LUSC specimens (2-3 mm3), which were from Shanghai Chest Hospital, were implanted into 4- to 6-week-old athymic nude mice (Jiesijie, Shanghai, China). After successful tumor growth was confirmed, the tumor tissues were passaged and implanted into the next generation of mice. The third to fifth generations of PDX-bearing mice were used for drug administration. When tumors reached approximately 200 mm3, mice were injected daily with DMSO (no. ST038, Beyotime Biotechnology, Shanghai, China) with or without MIT (no. S2485, 5 mg/kg, Selleck, Houston, TX) or HYD (no. S1896, 20 mg/kg, Selleck) (n = 5 mice/group). Tumor growth was monitored, and sizes were calculated by 0.5 × L × W2 (L indicating length and W indicating width). The mice were euthanized at day 28 after implantation. All animal experiments were approved by the institutional ethics committee of Shanghai Chest Hospital (approval number KS(Y)21380).
Hydroxyurea [Approved]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [38]
Target Regulation Up regulation
Pathway Response Wnt signaling pathway hsa04310
In-vitro Model BEAS-2B Normal Homo sapiens CVCL_0168
NCI-H1299 Lung large cell carcinoma Homo sapiens CVCL_0060
NCI-H1975 Lung adenocarcinoma Homo sapiens CVCL_1511
A-549 Lung adenocarcinoma Homo sapiens CVCL_0023
PC-9 Lung adenocarcinoma Homo sapiens CVCL_B260
BEL-7404 Endocervical adenocarcinoma Homo sapiens CVCL_6568
BEL-7402 Endocervical adenocarcinoma Homo sapiens CVCL_5492
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
SW1990 Pancreatic adenocarcinoma Homo sapiens CVCL_1723
PANC-1 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0480
MKN45 Gastric adenocarcinoma Homo sapiens CVCL_0434
MGC-803 Gastric mucinous adenocarcinoma Homo sapiens CVCL_5334
HCT 116 Colon carcinoma Homo sapiens CVCL_0291
HT29 Colon cancer Mus musculus CVCL_A8EZ
MCF-7 Invasive breast carcinoma Homo sapiens CVCL_0031
In-vivo Model For the generation of PDX mouse models, fresh LUSC specimens (2-3 mm3), which were from Shanghai Chest Hospital, were implanted into 4- to 6-week-old athymic nude mice (Jiesijie, Shanghai, China). After successful tumor growth was confirmed, the tumor tissues were passaged and implanted into the next generation of mice. The third to fifth generations of PDX-bearing mice were used for drug administration. When tumors reached approximately 200 mm3, mice were injected daily with DMSO (no. ST038, Beyotime Biotechnology, Shanghai, China) with or without MIT (no. S2485, 5 mg/kg, Selleck, Houston, TX) or HYD (no. S1896, 20 mg/kg, Selleck) (n = 5 mice/group). Tumor growth was monitored, and sizes were calculated by 0.5 × L × W2 (L indicating length and W indicating width). The mice were euthanized at day 28 after implantation. All animal experiments were approved by the institutional ethics committee of Shanghai Chest Hospital (approval number KS(Y)21380).
Mitoxantrone [Approved]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [38]
Target Regulation Up regulation
Pathway Response Wnt signaling pathway hsa04310
In-vitro Model BEAS-2B Normal Homo sapiens CVCL_0168
NCI-H1299 Lung large cell carcinoma Homo sapiens CVCL_0060
NCI-H1975 Lung adenocarcinoma Homo sapiens CVCL_1511
A-549 Lung adenocarcinoma Homo sapiens CVCL_0023
PC-9 Lung adenocarcinoma Homo sapiens CVCL_B260
BEL-7404 Endocervical adenocarcinoma Homo sapiens CVCL_6568
BEL-7402 Endocervical adenocarcinoma Homo sapiens CVCL_5492
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
SW1990 Pancreatic adenocarcinoma Homo sapiens CVCL_1723
PANC-1 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0480
MKN45 Gastric adenocarcinoma Homo sapiens CVCL_0434
MGC-803 Gastric mucinous adenocarcinoma Homo sapiens CVCL_5334
HCT 116 Colon carcinoma Homo sapiens CVCL_0291
HT29 Colon cancer Mus musculus CVCL_A8EZ
MCF-7 Invasive breast carcinoma Homo sapiens CVCL_0031
In-vivo Model For the generation of PDX mouse models, fresh LUSC specimens (2-3 mm3), which were from Shanghai Chest Hospital, were implanted into 4- to 6-week-old athymic nude mice (Jiesijie, Shanghai, China). After successful tumor growth was confirmed, the tumor tissues were passaged and implanted into the next generation of mice. The third to fifth generations of PDX-bearing mice were used for drug administration. When tumors reached approximately 200 mm3, mice were injected daily with DMSO (no. ST038, Beyotime Biotechnology, Shanghai, China) with or without MIT (no. S2485, 5 mg/kg, Selleck, Houston, TX) or HYD (no. S1896, 20 mg/kg, Selleck) (n = 5 mice/group). Tumor growth was monitored, and sizes were calculated by 0.5 × L × W2 (L indicating length and W indicating width). The mice were euthanized at day 28 after implantation. All animal experiments were approved by the institutional ethics committee of Shanghai Chest Hospital (approval number KS(Y)21380).
Oxaliplatin [Approved]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [38]
Target Regulation Up regulation
Pathway Response Wnt signaling pathway hsa04310
In-vitro Model BEAS-2B Normal Homo sapiens CVCL_0168
NCI-H1299 Lung large cell carcinoma Homo sapiens CVCL_0060
NCI-H1975 Lung adenocarcinoma Homo sapiens CVCL_1511
A-549 Lung adenocarcinoma Homo sapiens CVCL_0023
PC-9 Lung adenocarcinoma Homo sapiens CVCL_B260
BEL-7404 Endocervical adenocarcinoma Homo sapiens CVCL_6568
BEL-7402 Endocervical adenocarcinoma Homo sapiens CVCL_5492
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
SW1990 Pancreatic adenocarcinoma Homo sapiens CVCL_1723
PANC-1 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0480
MKN45 Gastric adenocarcinoma Homo sapiens CVCL_0434
MGC-803 Gastric mucinous adenocarcinoma Homo sapiens CVCL_5334
HCT 116 Colon carcinoma Homo sapiens CVCL_0291
HT29 Colon cancer Mus musculus CVCL_A8EZ
MCF-7 Invasive breast carcinoma Homo sapiens CVCL_0031
In-vivo Model For the generation of PDX mouse models, fresh LUSC specimens (2-3 mm3), which were from Shanghai Chest Hospital, were implanted into 4- to 6-week-old athymic nude mice (Jiesijie, Shanghai, China). After successful tumor growth was confirmed, the tumor tissues were passaged and implanted into the next generation of mice. The third to fifth generations of PDX-bearing mice were used for drug administration. When tumors reached approximately 200 mm3, mice were injected daily with DMSO (no. ST038, Beyotime Biotechnology, Shanghai, China) with or without MIT (no. S2485, 5 mg/kg, Selleck, Houston, TX) or HYD (no. S1896, 20 mg/kg, Selleck) (n = 5 mice/group). Tumor growth was monitored, and sizes were calculated by 0.5 × L × W2 (L indicating length and W indicating width). The mice were euthanized at day 28 after implantation. All animal experiments were approved by the institutional ethics committee of Shanghai Chest Hospital (approval number KS(Y)21380).
Raltitrexed [Approved]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [38]
Target Regulation Up regulation
Pathway Response Wnt signaling pathway hsa04310
In-vitro Model BEAS-2B Normal Homo sapiens CVCL_0168
NCI-H1299 Lung large cell carcinoma Homo sapiens CVCL_0060
NCI-H1975 Lung adenocarcinoma Homo sapiens CVCL_1511
A-549 Lung adenocarcinoma Homo sapiens CVCL_0023
PC-9 Lung adenocarcinoma Homo sapiens CVCL_B260
BEL-7404 Endocervical adenocarcinoma Homo sapiens CVCL_6568
BEL-7402 Endocervical adenocarcinoma Homo sapiens CVCL_5492
Hep-G2 Hepatoblastoma Homo sapiens CVCL_0027
SW1990 Pancreatic adenocarcinoma Homo sapiens CVCL_1723
PANC-1 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0480
MKN45 Gastric adenocarcinoma Homo sapiens CVCL_0434
MGC-803 Gastric mucinous adenocarcinoma Homo sapiens CVCL_5334
HCT 116 Colon carcinoma Homo sapiens CVCL_0291
HT29 Colon cancer Mus musculus CVCL_A8EZ
MCF-7 Invasive breast carcinoma Homo sapiens CVCL_0031
In-vivo Model For the generation of PDX mouse models, fresh LUSC specimens (2-3 mm3), which were from Shanghai Chest Hospital, were implanted into 4- to 6-week-old athymic nude mice (Jiesijie, Shanghai, China). After successful tumor growth was confirmed, the tumor tissues were passaged and implanted into the next generation of mice. The third to fifth generations of PDX-bearing mice were used for drug administration. When tumors reached approximately 200 mm3, mice were injected daily with DMSO (no. ST038, Beyotime Biotechnology, Shanghai, China) with or without MIT (no. S2485, 5 mg/kg, Selleck, Houston, TX) or HYD (no. S1896, 20 mg/kg, Selleck) (n = 5 mice/group). Tumor growth was monitored, and sizes were calculated by 0.5 × L × W2 (L indicating length and W indicating width). The mice were euthanized at day 28 after implantation. All animal experiments were approved by the institutional ethics committee of Shanghai Chest Hospital (approval number KS(Y)21380).
Translation machinery-associated protein 7 (TMA7)
Cisplatin [Approved]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [59]
Responsed Disease Laryngeal cancer ICD-11: 2C23
Target Regulation Up regulation
In-vitro Model Tu 212 Head and neck squamous cell carcinoma Homo sapiens CVCL_4915
Tu 177 Laryngeal squamous cell carcinoma Homo sapiens CVCL_4913
AMC-HN-8 Laryngeal squamous cell carcinoma Homo sapiens CVCL_5966
In-vivo Model Male BALB/c nude mice (4-weeks-old; body weight 20-25 g; n=15) were obtained from Vital River Laboratories (Beijing, China) and maintained at 20-26 °C and 40-70% humidity with specific pathogen-free conditions. The mice were divided into control, TMA7 KD, and TMA7 KD+UBA2 OE groups. Each nude mouse was injected with 100 μL (1.0x107 cells) of lentivirus-transfected LSCC cells. The formula length×width 2×0.5 was used to calculate the tumor volume. 34 days after inoculation, the xenografts were excised, and their volume was determined.
Trinucleotide repeat-containing gene 6A protein (TNRC6A)
Sunitinib [Approved]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [11]
Responsed Disease Renal cell carcinoma ICD-11: 2C90
In-vitro Model ACHN Papillary renal cell carcinoma Homo sapiens CVCL_1067
A-498 Renal cell carcinoma Homo sapiens CVCL_1056
Caki-1 Clear cell renal cell carcinoma Homo sapiens CVCL_0234
OS-RC-2 Clear cell renal cell carcinoma Homo sapiens CVCL_1626
786-O Renal cell carcinoma Homo sapiens CVCL_1051
HK-2 [Human kidney] Normal Homo sapiens CVCL_0302
In-vivo Model A total of 1 × 106 ACHN cells was injected into left renal capsule (n = 5 mice/group). Then, we sutured the wound layer by layer. Tumour size was measured 4 weeks later with in-Vivo FX PRO small animal imaging system (BRUKER). After that, we executed the mice and collected tumours for immunohistochemistry (IHC) assays and Western blotting. For metastasis model construction, 1 × 106 ACHN cells were injected into tail-vein of each mouse (n = 5 mice/group).
Zinc finger MIZ domain-containing protein 2 (ZMIZ2)
Sunitinib [Approved]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [11]
Responsed Disease Renal cell carcinoma ICD-11: 2C90
In-vitro Model ACHN Papillary renal cell carcinoma Homo sapiens CVCL_1067
A-498 Renal cell carcinoma Homo sapiens CVCL_1056
Caki-1 Clear cell renal cell carcinoma Homo sapiens CVCL_0234
OS-RC-2 Clear cell renal cell carcinoma Homo sapiens CVCL_1626
786-O Renal cell carcinoma Homo sapiens CVCL_1051
HK-2 [Human kidney] Normal Homo sapiens CVCL_0302
In-vivo Model A total of 1 × 106 ACHN cells was injected into left renal capsule (n = 5 mice/group). Then, we sutured the wound layer by layer. Tumour size was measured 4 weeks later with in-Vivo FX PRO small animal imaging system (BRUKER). After that, we executed the mice and collected tumours for immunohistochemistry (IHC) assays and Western blotting. For metastasis model construction, 1 × 106 ACHN cells were injected into tail-vein of each mouse (n = 5 mice/group).
Unspecific Target Gene
Gemcitabine [Approved]
In total 1 item(s) under this drug
Experiment 1 Reporting the m6A-centered Drug Response of This Target Gene [60]
Responsed Disease Pancreatic cancer ICD-11: 2C10
Pathway Response Adipocytokine signaling pathway hsa04920
Cell Process Epithelial-mesenchymal transition
In-vitro Model BxPC-3 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0186
HDE-CT cell line (A normal human pancreatic cell line)
MIA PaCa-2 Pancreatic ductal adenocarcinoma Homo sapiens CVCL_0428
Response Summary Lasso regression identified a six-m6A-regulator-signature prognostic model (KIAA1429, HNRNPC, METTL3, YTHDF1, IGF2BP2, and IGF2BP3). Gene set enrichment analysis revealed m6A regulators (KIAA1429, HNRNPC, and IGF2BP2) were related to multiple biological behaviors in pancreatic cancer, including adipocytokine signaling, the well vs. poorly differentiated tumor pathway, tumor metastasis pathway, epithelial mesenchymal transition pathway, gemcitabine resistance pathway, and stemness pathway.
Full List of Crosstalk(s) between m6A Modification and Epigenetic Regulation Related to This Regulator
RNA modification
m6A Target: Glutaminase kidney isoform, mitochondrial (GLS)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT00072
Epigenetic Regulator RNA cytosine C(5)-methyltransferase NSUN2 (NSUN2)
Regulated Target TNFRSF10A divergent transcript (TNFRSF10A-DT)
Crosstalk relationship m5C → m6A
Disease Gastric cancer
m6A Target: Cellular tumor antigen p53 (TP53/p53)
In total 2 item(s) under this m6A target
Crosstalk ID: M6ACROT00431
Epigenetic Regulator Methyltransferase-like protein 1 (METTL1)
Regulated Target MicroRNA 125a (MIR125A)
Crosstalk relationship m7G → m6A
Crosstalk ID: M6ACROT00436
Epigenetic Regulator Double-stranded RNA-specific editase 1 (ADARB1)
Regulated Target MicroRNA 214 (MIR214)
Crosstalk relationship A-to-I → m6A
m6A Target: Cyclin-dependent kinase 6 (CDK6)
In total 2 item(s) under this m6A target
Crosstalk ID: M6ACROT00453
Epigenetic Regulator Interferon-inducible protein 4 (ADAR1)
Regulated Target MicroRNA 149 (MIR149)
Crosstalk relationship A-to-I → m6A
Crosstalk ID: M6ACROT00454
Epigenetic Regulator Methyltransferase-like protein 1 (METTL1)
Regulated Target MicroRNA 149 (MIR149)
Crosstalk relationship m7G → m6A
m6A Target: Glucose transporter type 1 (GLUT1)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT00490
Epigenetic Regulator Fat mass and obesity-associated protein (FTO)
Regulated Target hsa-mir-22
Crosstalk relationship m6Am → m6A
m6A Target: Cyclin-dependent kinase inhibitor 1B (CDKN1B/p27)
In total 2 item(s) under this m6A target
Crosstalk ID: M6ACROT00495
Epigenetic Regulator Double-stranded RNA-specific editase 1 (ADARB1)
Regulated Target MicroRNA 222 (MIR222)
Crosstalk relationship A-to-I → m6A
Crosstalk ID: M6ACROT00496
Epigenetic Regulator Interferon-inducible protein 4 (ADAR1)
Regulated Target MicroRNA 222 (MIR222)
Crosstalk relationship A-to-I → m6A
m6A Target: Hypoxia-inducible factor 1-alpha (HIF-1-Alpha/HIF1A)
In total 2 item(s) under this m6A target
Crosstalk ID: M6ACROT00526
Epigenetic Regulator Double-stranded RNA-specific editase 1 (ADARB1)
Regulated Target MicroRNA 142 (MIR142)
Crosstalk relationship A-to-I → m6A
Crosstalk ID: M6ACROT00530
Epigenetic Regulator Fat mass and obesity-associated protein (FTO)
Regulated Target MicroRNA 576 (MIR576)
Crosstalk relationship m6Am → m6A
m6A Target: Insulin-like growth factor 2 (IGF2)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT00538
Epigenetic Regulator Interferon-inducible protein 4 (ADAR1)
Regulated Target MicroRNA 432 (MIR432)
Crosstalk relationship A-to-I → m6A
m6A Target: Fascin (FSCN1)
In total 2 item(s) under this m6A target
Crosstalk ID: M6ACROT00548
Epigenetic Regulator Interferon-inducible protein 4 (ADAR1)
Regulated Target MicroRNA 200b (MIR200B)
Crosstalk relationship A-to-I → m6A
Crosstalk ID: M6ACROT00549
Epigenetic Regulator Y-box-binding protein 1 (YBX1)
Regulated Target MicroRNA 200b (MIR200B)
Crosstalk relationship m5C → m6A
DNA modification
m6A Target: Semaphorin-3F (SEMA3F)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT02017
Epigenetic Regulator DNA (cytosine-5)-methyltransferase 1 (DNMT1)
Regulated Target Semaphorin-3F (SEMA3F)
Crosstalk relationship m6A → DNA modification
Disease Prostate cancer
Drug Docetaxel
m6A Target: Cysteine methyltransferase DNMT3A (DNMT3A)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT02107
Epigenetic Regulator Cysteine methyltransferase DNMT3A (DNMT3A)
Crosstalk relationship m6A → DNA modification
Disease Gastric cancer
Drug Decitabine
Histone modification
m6A Target: JmjC domain-containing protein 8 (JMJD8)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT03103
Epigenetic Regulator Histone deacetylase 2 (HDAC2)
Regulated Target Histone H3 lysine 27 acetylation (H3K27ac)
Crosstalk relationship Histone modification → m6A
Disease Colorectal cancer
m6A Target: Histone-lysine N-methyltransferase SETMAR (SETMAR)
In total 3 item(s) under this m6A target
Crosstalk ID: M6ACROT03112
Epigenetic Regulator Histone-lysine N-methyltransferase SETMAR (SETMAR)
Regulated Target Histone H3 lysine 36 dimethylation (H3K36me2)
Crosstalk relationship m6A → Histone modification
Disease Thyroid Cancer
Crosstalk ID: M6ACROT03114
Epigenetic Regulator Probable global transcription activator SNF2L2 (SMARCA2)
Regulated Target Histone H3 lysine 27 acetylation (H3K27ac)
Crosstalk relationship m6A → Histone modification
Disease Thyroid Cancer
Crosstalk ID: M6ACROT05849
Epigenetic Regulator Probable global transcription activator SNF2L2 (SMARCA2)
Regulated Target Histone H3 lysine 27 acetylation (H3K27ac)
Crosstalk relationship m6A → Histone modification
Disease Thyroid Cancer
m6A Target: SUMO specific peptidase 1 (SENP1)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT03115
Epigenetic Regulator Histone deacetylase 2 (HDAC2)
Regulated Target Epidermal growth factor receptor (EGFR)
Crosstalk relationship m6A → Histone modification
Disease Acute myeloid leukaemia
m6A Target: Histone deacetylase 9 (HDAC9)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT03188
Epigenetic Regulator Histone deacetylase 9 (HDAC9)
Regulated Target Histone H4 lysine 12 acetylation (H4K12ac)
Crosstalk relationship m6A → Histone modification
Disease Acute laryngitis or tracheitis
m6A Target: Histone deacetylase 3 (HDAC3)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT03207
Epigenetic Regulator Histone deacetylase 3 (HDAC3)
Crosstalk relationship m6A → Histone modification
Disease Acute ischemic stroke
m6A Target: Homeobox protein Hox-A13 (HOXA13)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT03230
Epigenetic Regulator PHD finger protein 20 (PHF20)
Regulated Target Histone H3 lysine 4 trimethylation (H3K4me3)
Crosstalk relationship Histone modification → m6A
m6A Target: Pirin (PIR)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT03234
Epigenetic Regulator WD repeat-containing protein 5 (WDR5)
Regulated Target Histone H3 lysine 4 trimethylation (H3K4me3)
Crosstalk relationship m6A → Histone modification
Disease Melanoma of uvea
m6A Target: Hexokinase-2 (HK2)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT03369
Epigenetic Regulator Histone deacetylase 2 (HDAC2)
Regulated Target Histone H3 lysine 27 acetylation (H3K27ac)
Crosstalk relationship Histone modification → m6A
Disease Colorectal cancer
Non-coding RNA
m6A Target: TNF receptor-associated factor 5 (TRAF5)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT05006
Epigenetic Regulator Long intergenic non-protein coding RNA 467 (LINC00467)
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Liver cancer
m6A Target: E3 ubiquitin-protein ligase ZNRF3 (ZNRF3)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT05007
Epigenetic Regulator RMRP
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Brain cancer
Drug Temozolomide
m6A Target: Thymidine kinase, cytosolic (TK1)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT05011
Epigenetic Regulator DARS1 antisense RNA 1 (DARS1-AS1)
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Cervical cancer
m6A Target: Myc proto-oncogene protein (MYC)
In total 2 item(s) under this m6A target
Crosstalk ID: M6ACROT05012
Epigenetic Regulator DARS1 antisense RNA 1 (DARS1-AS1)
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Cervical cancer
Crosstalk ID: M6ACROT05216
Epigenetic Regulator LOC101929709
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Gastric cancer
m6A Target: Fascin (FSCN1)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT05013
Epigenetic Regulator DARS1 antisense RNA 1 (DARS1-AS1)
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Cervical cancer
m6A Target: MARCKS-related protein (MARCKSL1)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT05014
Epigenetic Regulator DARS1 antisense RNA 1 (DARS1-AS1)
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Cervical cancer
m6A Target: KCNMB2 antisense RNA 1 (KCNMB2-AS1)
In total 6 item(s) under this m6A target
Crosstalk ID: M6ACROT05015
Epigenetic Regulator DARS1 antisense RNA 1 (DARS1-AS1)
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Cervical cancer
Crosstalk ID: M6ACROT05331
Epigenetic Regulator KCNMB2 antisense RNA 1 (KCNMB2-AS1)
Regulated Target hsa-miR-130b-5p
Crosstalk relationship ncRNA → m6A
Disease Cervical cancer
Crosstalk ID: M6ACROT05332
Epigenetic Regulator KCNMB2 antisense RNA 1 (KCNMB2-AS1)
Regulated Target hsa-miR-4294
Crosstalk relationship ncRNA → m6A
Disease Cervical cancer
Crosstalk ID: M6ACROT05333
Epigenetic Regulator hsa-miR-130b-5p
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Cervical cancer
Crosstalk ID: M6ACROT05334
Epigenetic Regulator hsa-miR-4294
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Cervical cancer
Crosstalk ID: M6ACROT05448
Epigenetic Regulator KCNMB2 antisense RNA 1 (KCNMB2-AS1)
Regulated Target hsa-miR-130b-5p
Crosstalk relationship m6A → ncRNA
Disease Cervical cancer
m6A Target: Apoptotic chromatin condensation inducer in the nucleus (ACIN1)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT05016
Epigenetic Regulator DARS1 antisense RNA 1 (DARS1-AS1)
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Cervical cancer
m6A Target: Glutaminase kidney isoform, mitochondrial (GLS)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT05017
Epigenetic Regulator DARS1 antisense RNA 1 (DARS1-AS1)
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Cervical cancer
m6A Target: Glutamate dehydrogenase 1, mitochondrial (GLUD1)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT05018
Epigenetic Regulator DARS1 antisense RNA 1 (DARS1-AS1)
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Cervical cancer
m6A Target: Stearoyl-CoA desaturase (SCD)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT05019
Epigenetic Regulator DARS1 antisense RNA 1 (DARS1-AS1)
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Cervical cancer
m6A Target: 5-hydroxytryptamine receptor 3A (HTR3A)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT05022
Epigenetic Regulator Long intergenic non-protein coding RNA 1305 (LINC01305)
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Esophageal Squamous Cell Carcinoma
m6A Target: Protein diaphanous homolog 3 (DIAPH3)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT05126
Epigenetic Regulator Long intergenic non-protein coding RNA 1089 (LINC01089)
Regulated Target Heterogeneous nuclear ribonucleoprotein M (HNRNPM)
Crosstalk relationship ncRNA → m6A
Disease Liver cancer
m6A Target: Hexokinase-3 (HK3)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT05229
Epigenetic Regulator Circ_ZBTB44
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Renal cell carcinoma
m6A Target: High mobility group protein B1 (HMGB1)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT05266
Epigenetic Regulator hsa-miR-320a-3p
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Bladder cancer
Drug Glycyrrhizin
m6A Target: Cystine/glutamate transporter (SLC7A11)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT05273
Epigenetic Regulator Long intergenic non-protein coding RNA 942 (LINC00942)
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Liver cancer
m6A Target: Metastasis associated lung adenocarcinoma transcript 1 (MALAT1)
In total 3 item(s) under this m6A target
Crosstalk ID: M6ACROT05275
Epigenetic Regulator hsa_circ_0004287 (Circ_MALAT1)
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Atopic eczema
Crosstalk ID: M6ACROT05638
Epigenetic Regulator Metastasis associated lung adenocarcinoma transcript 1 (MALAT1)
Regulated Target Protein S100-A8 (S100A8)
Crosstalk relationship m6A → ncRNA
Disease Atopic eczema
Crosstalk ID: M6ACROT06028
Epigenetic Regulator Metastasis associated lung adenocarcinoma transcript 1 (MALAT1)
Regulated Target Protein S100-A9 (S100A9)
Crosstalk relationship m6A → ncRNA
Disease Atopic eczema
m6A Target: Collagen alpha-1 (COL6A1)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT05298
Epigenetic Regulator DMDRMR
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Renal cell carcinoma of kidney
m6A Target: Laminin subunit alpha-5 (LAMA5)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT05299
Epigenetic Regulator DMDRMR
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Renal cell carcinoma of kidney
m6A Target: Fibronectin (FN1)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT05300
Epigenetic Regulator DMDRMR
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Renal cell carcinoma of kidney
m6A Target: Glucose transporter type 1 (SLC2A1)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT05341
Epigenetic Regulator Circ_FOXK2
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship ncRNA → m6A
Disease Oral squamous cell carcinoma
m6A Target: long intergenic non-protein coding RNA 632 (LINC00632)
In total 3 item(s) under this m6A target
Crosstalk ID: M6ACROT05413
Epigenetic Regulator Long intergenic non-protein coding RNA 632 (LINC00632)
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship m6A → ncRNA
Disease Non-small cell lung cancer
Drug Cisplatin
Crosstalk ID: M6ACROT05414
Epigenetic Regulator Long intergenic non-protein coding RNA 632 (LINC00632)
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship m6A → ncRNA
Disease Esophageal cancer
Drug Cisplatin
Crosstalk ID: M6ACROT05415
Epigenetic Regulator Long intergenic non-protein coding RNA 632 (LINC00632)
Regulated Target Insulin like growth factor 2 mRNA binding protein 3 (IGF2BP3)
Crosstalk relationship m6A → ncRNA
Disease Esophageal cancer
Drug Cisplatin
m6A Target: DMDRMR
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT05454
Epigenetic Regulator DMDRMR
Crosstalk relationship m6A → ncRNA
Disease Renal cell carcinoma
m6A Target: hsa_circ_0004287
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT05637
Epigenetic Regulator hsa_circ_0004287 (Circ_MALAT1)
Regulated Target Metastasis associated lung adenocarcinoma transcript 1 (MALAT1)
Crosstalk relationship m6A → ncRNA
Disease Atopic eczema
m6A Target: RNA component of 7SK nuclear ribonucleoprotein (RN7SK)
In total 5 item(s) under this m6A target
Crosstalk ID: M6ACROT05659
Epigenetic Regulator RNA component of 7SK nuclear ribonucleoprotein (RN7SK)
Regulated Target Cullin 1 (CUL1)
Crosstalk relationship m6A → ncRNA
Drug mitoxantrone (MIT)
Crosstalk ID: M6ACROT06029
Epigenetic Regulator RNA component of 7SK nuclear ribonucleoprotein (RN7SK)
Regulated Target Cullin 1 (CUL1)
Crosstalk relationship m6A → ncRNA
Drug hydroxyurea (HYD)
Crosstalk ID: M6ACROT06032
Epigenetic Regulator RNA component of 7SK nuclear ribonucleoprotein (RN7SK)
Regulated Target Cullin 1 (CUL1)
Crosstalk relationship m6A → ncRNA
Drug raltitrexed (RAL)
Crosstalk ID: M6ACROT06035
Epigenetic Regulator RNA component of 7SK nuclear ribonucleoprotein (RN7SK)
Regulated Target Cullin 1 (CUL1)
Crosstalk relationship m6A → ncRNA
Drug oxaliplatin (OXA)
Crosstalk ID: M6ACROT06038
Epigenetic Regulator RNA component of 7SK nuclear ribonucleoprotein (RN7SK)
Regulated Target Cullin 1 (CUL1)
Crosstalk relationship m6A → ncRNA
Drug etoposide (ETO)
m6A Target: Long intergenic non-protein coding RNA 662 (LINC00662)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT05700
Epigenetic Regulator Long intergenic non-protein coding RNA 662 (LINC00662)
Regulated Target Integrin subunit alpha 1 (ITGA1)
Crosstalk relationship m6A → ncRNA
Disease Pancreatic cancer
m6A Target: Cysteine methyltransferase DNMT3A (DNMT3A)
In total 1 item(s) under this m6A target
Crosstalk ID: M6ACROT05962
Epigenetic Regulator Long intergenic non-protein coding RNA 942 (LINC00942)
Regulated Target Methyltransferase-like protein 3 (METTL3)
Crosstalk relationship ncRNA → m6A
Disease Gastric cancer
Drug Decitabine
Xenobiotics Compound(s) Regulating the m6A Methylation Regulator
Compound Name Linsitinib Phase 3
Synonyms
Linsitinib; 867160-71-2; OSI-906; Linsitinib(OSI-906); OSI906; OSI 906; OSI-906AA; OSI-906 (Linsitinib); UNII-15A52GPT8T; Kinome_3532; ASP-7487; 3-[8-amino-1-(2-phenylquinolin-7-yl)imidazo[1,5-a]pyrazin-3-yl]-1-methylcyclobutan-1-ol; 15A52GPT8T; CHEMBL1091644; MMV676605; cis-3-[8-Amino-1-(2-phenyl-7-quinolinyl)imidazo[1,5-a]pyrazin-3-yl]-1-methylcyclobutanol; C26H23N5O; cis-3-(8-amino-1-(2-phenyl-7-quinolinyl)imidazo(1,5-a)pyrazin-3-yl)-1-methylcyclobutanol; Linsitinib [USAN:INN]; OSI906/Linsitinib/; Linsitinib; OSI-906
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Description
The m6A reader YTHDF2 stabilizedMYC mRNA specifically in cancer stem cells. Given the challenge of targeting MYC, YTHDF2 presents a therapeutic target to perturb MYC signaling in glioblastoma. The IGF1/IGF1R inhibitor linsitinib preferentially targeted YTHDF2-expressing cells, inhibiting GSC viability without affecting NSCs and impairing in vivoglioblastoma growth. YTHDF2 links RNA epitranscriptomic modifications and GSC growth, laying the foundation for the YTHDF2-MYC-IGFBP3 axis as a specific and novel therapeutic target in glioblastoma.
[24]
Compound Name PMID29703820-Compound-JQ1 Investigative
Description
The bromodomain and extraterminal domain inhibitor (BETi) JQ1 decreased IGF2BP3 expression.
[64]
References
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