m6A-centered Crosstalk Information

Mechanism of Crosstalk between m6A Modification and Epigenetic Regulation
Crosstalk ID
M6ACROT05276
 [1]
Non-coding RNA MIR100HG HNRNPA2B1  lncRNA       miRNA   circRNA Direct Enhancement m6A modification TCF7L2 TCF7L2 hnRNPA2B1 : m6A sites
m6A Modification:
m6A Regulator Heterogeneous nuclear ribonucleoproteins A2/B1 (HNRNPA2B1) READER
 Regulator Info 
m6A Target Transcription factor 7-like 2 (TCF7L2)
 Targert Gene 
Epigenetic Regulation that have Cross-talk with This m6A Modification:
Epigenetic Regulation Type Non-coding RNA (ncRNA)
Epigenetic Regulator Mir-100-let-7a-2-mir-125b-1 cluster host gene (MIR100HG) LncRNA View Details
Regulated Target Heterogeneous nuclear ribonucleoprotein A2/B1 (HNRNPA2B1) View Details
Crosstalk Relationship ncRNA  →  m6A Enhancement
Crosstalk Mechanism ncRNAs directly impacts m6A modification through recruiting m6A regulator
Crosstalk Summary MIR100HG maintained mRNA stability of Transcription factor 7-like 2 (TCF7L2), a major transcriptional coactivator of the Wnt/beta-catenin signaling, by interacting with HNRNPA2B1. hnRNPA2B1 recognized the N6-methyladenosine (m6A) site of TCF7L2 mRNA in the presence of MIR100HG.
Responsed Disease Colorectal cancer ICD-11: 2B91
 Disease Info 
Responsed Drug Cetuximab
 Drug Info 
Pathway Response Wnt signaling pathway hsa04310
Cell Process Epithelial-mesenchymal transition
In-vitro Model
 NCI-H508 Cecum adenocarcinoma Homo sapiens CVCL_1564
Caco-2 Colon adenocarcinoma Homo sapiens CVCL_0025
SW403 Colon adenocarcinoma Homo sapiens CVCL_0545
SW948 Colon adenocarcinoma Homo sapiens CVCL_0632
HT29 Colon cancer Mus musculus CVCL_A8EZ
SK-CO-1 Colon adenocarcinoma Homo sapiens CVCL_0626
DLD-1 Colon adenocarcinoma Homo sapiens CVCL_0248
SW480 Colon adenocarcinoma Homo sapiens CVCL_0546
SW837 Rectal adenocarcinoma Homo sapiens CVCL_1729
SW48 Colon adenocarcinoma Homo sapiens CVCL_1724
SW620 Colon adenocarcinoma Homo sapiens CVCL_0547
LoVo Colon adenocarcinoma Homo sapiens CVCL_0399
COLO205
 N.A. Homo sapiens CVCL_F402
T84 Colon adenocarcinoma Homo sapiens CVCL_0555
LS174T Colon adenocarcinoma Homo sapiens CVCL_1384
NCI-H716 Cecum adenocarcinoma Homo sapiens CVCL_1581
HCT 8 Colon adenocarcinoma Homo sapiens CVCL_2478
HCT 15 Colon adenocarcinoma Homo sapiens CVCL_0292
SW1116 Colon adenocarcinoma Homo sapiens CVCL_0544
RKO Colon carcinoma Homo sapiens CVCL_0504
COLO 320DM Colon adenocarcinoma Homo sapiens CVCL_0219
HuTu 80 Duodenal adenocarcinoma Homo sapiens CVCL_1301
LS123 Colon adenocarcinoma Homo sapiens CVCL_1383
HCT 116 Colon carcinoma Homo sapiens CVCL_0291
DiFi Colorectal carcinoma Homo sapiens CVCL_6895
GEO Colon carcinoma Homo sapiens CVCL_0271
LIM1215 Colon adenocarcinoma Homo sapiens CVCL_2574
LIM2405 Cecum adenocarcinoma Homo sapiens CVCL_4437
VACO 9P Rectal adenocarcinoma Homo sapiens CVCL_5413
Full List of Potential Compound(s) Related to This m6A-centered Crosstalk
2B91: Colorectal cancer 25 Compound(s) Regulating the Disease Click to Show/Hide the Full List
 Compound Name Retifanlimab Approved [2]
Synonyms
INCMGA0012; Retifanlimab
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TTD: D0PG5O
 Compound Name Aflibercept Approved [3]
Synonyms
Ziv-Aflibercept; Zaltrap (TN); VEGF Trap; VEGF Trap-Eye
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TTD: D0C9ET
 Compound Name Regorafenib Approved [4]
Synonyms
755037-03-7; BAY 73-4506; Regorafenibum; Stivarga; 4-(4-(3-(4-Chloro-3-(trifluoromethyl)phenyl)ureido)-3-fluorophenoxy)-N-methylpicolinamide; BAY73-4506; Regorafenib (BAY 73-4506); UNII-24T2A1DOYB; 4-[4-({[4-Chloro-3-(trifluoromethyl)phenyl]carbamoyl}amino)-3-fluorophenoxy]-N-methylpyridine-2-carboxamide; BAY-73-4506; 24T2A1DOYB; CHEMBL1946170; CHEBI:68647; Stivarga (TN); BAY73-4506 hydrochloride; Regorafenib [USAN:INN]
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CID: 11167602
TTD: D09GDD
DrugBank: DB08896
 Compound Name Bevacizumab Approved [5]
Synonyms
Bevacizumab (ophthalmic slow-release tissue tablet)
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TTD: D04KBL
 Compound Name SYM-004 Phase 3 [5]
Synonyms
Chimeric IgG1 antibody 1024 (cancer), Symphogen; Chimeric IgG1 antibody 992 (cancer), Symphogen; Chimeric IgG1 antibodies992 + 1024 (cancer), Symphogen
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TTD: D0CR8H
 Compound Name Bevacizumab + Erlotinib Phase 3 [6]
External Link
TTD: D09BKY
 Compound Name CPI-613 Phase 3 [5]
Synonyms
95809-78-2; 6,8-bis(benzylthio)octanoic acid; CPI 613; MLS006010202; SCHEMBL1062218; 6,8-Bis(benzylsulfanyl)octanoic acid; Octanoic acid, 6,8-bis((phenylmethyl)thio)-; Octanoic acid, 6,8-bis[(phenylMethyl)thio]-; 6,8-Bis[(phenylmethyl)thio]octanoic acid; CPI613; CHEMBL3186849; QCR-193; AOB1058; MolPort-023-219-128; HMS3656L06; C22H28O2S2; BCP04663; EX-A2043; s2776; AKOS025142095; BCP9000552; DB12109; RL06062; CS-0961; NCGC00344764-01; SMR004701300; AS-16613; BC261916; AK174899; HY-15453; BCP0726000030; KB-293127; AB0035874
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CID: 24770514
TTD: D07NVI
DrugBank: DB12109
 Compound Name Bevacizumab Approved [3]
External Link
TTD: D0FX3U
 Compound Name AlloStim Phase 2/3 [7]
Synonyms
AlloStim (TN)
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TTD: D0B3CC
 Compound Name Sibrotuzumab Phase 2 [8]
External Link
TTD: DVX3H0
 Compound Name CV301 Phase 2 [9]
External Link
TTD: D9LT5G
 Compound Name Efatutazone Phase 2 [10]
Synonyms
Inolitazone; 223132-37-4; 5-[[4-[[6-(4-amino-3,5-dimethylphenoxy)-1-methyl-1H-benzimidazol-2-yl]methoxy]phenyl]methyl]-2,4-Thiazolidinedione; Efatutazone [INN]; RS5444; CS-7017; SCHEMBL3246054; CHEMBL3545280; JCYNMRJCUYVDBC-UHFFFAOYSA-N; Efatutazone;CS-7017;RS5444; BCP07478; AKOS030526729; DB11894; CS-0778; KB-77905; DA-07988; HY-14792; QC-10456; 4CA-1384; FT-0737589; 5-[4-[6-(4-amino-3 ,5-dimethylphenoxy)-1-methyl-1H-benzimidazol-2-ylmethoxy]benzyl]thiazolidine-2,4-dione
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CID: 9832447
TTD: D0Y8NZ
DrugBank: DB11894
 Compound Name LOR-2040 Phase 2 [11]
External Link
TTD: D0I7NG
 Compound Name RG7221 Phase 2 [12]
External Link
TTD: D06FTM
 Compound Name PEG-SN38 Phase 2 [13]
Synonyms
EZN-2208
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CID: 59443782
TTD: D05UFP
 Compound Name MEGF0444A Phase 2 [14]
External Link
TTD: D01LES
 Compound Name Encapsulated cell therapy Phase 1/2 [15]
External Link
TTD: D0XY8C
 Compound Name AB928 Phase 1/2 [16]
External Link
CID: 135242184
TTD: D04UBI
 Compound Name MGD007 Phase 1 [12]
External Link
TTD: D00PEN
 Compound Name BNC-101 Phase 1 [17]
External Link
TTD: DD6AZ5
 Compound Name Navicixizumab Phase 1 [5]
External Link
TTD: D00IVN
 Compound Name RG7160 Discontinued in Phase 2 [18]
External Link
TTD: D0E2CQ
 Compound Name Nimesulide Terminated [19]
Synonyms
51803-78-2; N-(4-Nitro-2-phenoxyphenyl)methanesulfonamide; Mesulid; Flogovital; Sulidene; Nimed; R-805; 4-NITRO-2-PHENOXYMETHANESULFONANILIDE; Nisulid; Nimesulidum [INN-Latin]; Nimesulida [INN-Spanish]; R 805; UNII-V4TKW1454M; 4-Nitro-2-phenoxy-methanesulfonanilide; 4'-Nitro-2'-phenoxymethanesulfonanilide; Methanesulfonamide, N-(4-nitro-2-phenoxyphenyl)-; EINECS 257-431-4; 4'-Nitro-2'-phenoxymethansulfonanilid; BRN 2421175; CHEMBL56367; MLS000069680; V4TKW1454M; Methanesulfonanilide, 4'-nitro-2'-phenoxy-; CHEBI:44445; Dulanermin
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CID: 4495
TTD: D0C0JT
DrugBank: DB04743
 Compound Name Saracatinib Phase 2 [20]
External Link
CID: 10302451
TTD: D05YTN
DrugBank: DB11805
 Compound Name G3139 + Irinotecan Investigative [21]
External Link
CID: 91865905
TTD: D05IAN
References
Ref 1 Interaction of lncRNA MIR100HG with hnRNPA2B1 facilitates m(6)A-dependent stabilization of TCF7L2 mRNA and colorectal cancer progression. Mol Cancer. 2022 Mar 12;21(1):74. doi: 10.1186/s12943-022-01555-3.
Ref 2 Development of Inhibitors of the Programmed Cell Death-1/Programmed Cell Death-Ligand 1 Signaling Pathway.J Med Chem. 2019 Feb 28;62(4):1715-1730.
Ref 3 Drugs@FDA. U.S. Food and Drug Administration. U.S. Department of Health & Human Services. 2015
Ref 4 URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 5891).
Ref 5 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
Ref 6 ClinicalTrials.gov (NCT00130728) A Study to Evaluate the Efficacy of Bevacizumab in Combination With Tarceva for Advanced Non-Small Cell Lung Cancer
Ref 7 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
Ref 8 ClinicalTrials.gov (NCT02198274) Intravenous BIBH 1 in Patients With Metastatic Colorectal Cancer. U.S. National Institutes of Health.
Ref 9 ClinicalTrials.gov (NCT03547999) A Trial of Perioperative CV301 Vaccination in Combination With Nivolumab and Systemic Chemotherapy for Metastatic CRC. U.S. National Institutes of Health.
Ref 10 ClinicalTrials.gov (NCT02152137) Efatutazone With Paclitaxel Versus Paclitaxel Alone in Treating Patients With Advanced Anaplastic Thyroid Cancer. U.S. National Institutes of Health.
Ref 11 ClinicalTrials.gov (NCT00087165) GTI-2040, Docetaxel, and Prednisone in Treating Patients With Prostate Cancer. U.S. National Institutes of Health.
Ref 12 Clinical pipeline report, company report or official report of the Pharmaceutical Research and Manufacturers of America (PhRMA)
Ref 13 ClinicalTrials.gov (NCT01036113) A Phase 2 Study of EZN-2208 in Patients With Metastatic Breast Cancer. U.S. National Institutes of Health.
Ref 14 ClinicalTrials.gov (NCT00909740) A Study of the Safety and Pharmacokinetics of MEGF0444A Administered to Patients With Advanced Solid Tumors. U.S. National Institutes of Health.
Ref 15 VC-01's Path to the Clinic. Viacyte. 2015.
Ref 16 ClinicalTrials.gov (NCT04660812) An Open Label Study Evaluating the Efficacy and Safety of AB928 Based Treatment Combinations in Patients With Metastatic Colorectal Cancer.. U.S. National Institutes of Health.
Ref 17 ClinicalTrials.gov (NCT02726334) A Phase I, Dose Escalation Study of BNC101 in Patients With Metastatic Colorectal Cancer.. U.S. National Institutes of Health.
Ref 18 Trusted, scientifically sound profiles of drug programs, clinical trials, safety reports, and company deals, written by scientists. Springer. 2015. Adis Insight (drug id 800029052)
Ref 19 Clinical pipeline report, company report or official report of Genentech (2011).
Ref 20 Phase II Study of Saracatinib (AZD0530) in Patients With Previously Treated Metastatic Colorectal Cancer. Invest New Drugs. 2015 Aug;33(4):977-84.
Ref 21 Design and development of antisense drugs. Expert Opin. Drug Discov. 2008 3(10):1189-1207.