m6A-centered Crosstalk Information
Mechanism of Crosstalk between m6A Modification and Epigenetic Regulation
| Crosstalk ID |
M6ACROT03560
|
[1], [2] | |||
Histone modification
H3K27ac
EP300
LINC01605
Indirect
Enhancement
m6A modification
PTTG3P
PTTG3P
METTL3
Methylation
: m6A sites
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| m6A Modification: | |||||
|---|---|---|---|---|---|
| m6A Regulator | Methyltransferase-like 3 (METTL3) | WRITER | |||
| m6A Target | Putative pituitary tumor-transforming gene 3 protein (PTTG3P) | ||||
| Epigenetic Regulation that have Cross-talk with This m6A Modification: | |||||
| Epigenetic Regulation Type | Histone modification (HistMod) | ||||
| Epigenetic Regulator | Histone acetyltransferase p300 (P300) | WRITER | View Details | ||
| Regulated Target | Histone H3 lysine 27 acetylation (H3K27ac) | View Details | |||
| Downstream Gene | LINC01605 | View Details | |||
| Crosstalk Relationship | Histone modification → m6A | Enhancement | |||
| Crosstalk Mechanism | histone modification indirectly regulates m6A modification through downstream signaling pathways | ||||
| Crosstalk Summary | LINC01605 was regulated by SMYD2-p300-mediated modifications of histone H3K4me3 as well as Histone H3 lysine 27 acetylation (H3K27ac). LINC01605 was found to bind to METTL3 and promote the m6A modification of SPTBN2 mRNA, thereby facilitating the translation of SPTBN2. In colorectal cancer, n6-methyladenosine (m6A) subunit METTL3 increased PTTG3P expression by influencing its stability, while insulin-like growth factor 2 mRNA binding protein 2 (IGF2BP2) could identify Putative pituitary tumor-transforming gene 3 protein (PTTG3P) m6A methylation status and bind to it. | ||||
| Responsed Disease | Colorectal cancer | ICD-11: 2B91 | |||
| Pathway Response | Hippo signaling pathway | hsa04390 | |||
| Cell Process | Cell proliferation and suppression of apoptosis | ||||
In-vitro Model |
HT29 | Colon cancer | Mus musculus | CVCL_A8EZ | |
| SW620 | Colon adenocarcinoma | Homo sapiens | CVCL_0547 | ||
| HCT 8 | Colon adenocarcinoma | Homo sapiens | CVCL_2478 | ||
| SW480 | Colon adenocarcinoma | Homo sapiens | CVCL_0546 | ||
| HCT 116 | Colon carcinoma | Homo sapiens | CVCL_0291 | ||
| FHC | Normal | Homo sapiens | CVCL_3688 | ||
| NCM460 | Normal | Homo sapiens | CVCL_0460 | ||
| In-vivo Model | Indicated cells (1 × 107) were subcutaneously injected into 4-week-old male nude mice. Tumor volume was measured every 5 days. | ||||
Full List of Potential Compound(s) Related to This m6A-centered Crosstalk
| Histone acetyltransferase p300 (P300) | 2 Compound(s) Regulating the Target | Click to Show/Hide the Full List | ||
| CCS1477 | Phase 1/2 | [3] | ||
| Synonyms |
CCS-1477; CBP-IN-1; 2222941-37-7; (S)-1-(3,4-Difluorophenyl)-6-(5-(3,5-dimethylisoxazol-4-yl)-1-((1r,4S)-4-methoxycyclohexyl)-1H-benzo[d]imidazol-2-yl)piperidin-2-one; SCHEMBL20094038; SCHEMBL21515367; SCHEMBL22134021; EX-A3687; NSC818619; NSC-818619; HY-111784; CS-0091862; (S)-1-(3,4-Difluorophenyl)-6-(5-(3,5-dimethylisoxazol-4-yl)-1-(trans-4-methoxycyclohexyl)-1H-benzo[d]imidazol-2-yl)piperidin-2-one
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| MOA | Inhibitor | |||
| External Link | ||||
| FT-7051 | Phase 1 | [4] | ||
| MOA | Inhibitor | |||
| External Link | ||||
| 2B91: Colorectal cancer | 25 Compound(s) Regulating the Disease | Click to Show/Hide the Full List | ||
| Retifanlimab | Approved | [5] | ||
| Synonyms |
INCMGA0012; Retifanlimab
Click to Show/Hide
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| External Link | ||||
| Aflibercept | Approved | [6] | ||
| Synonyms |
Ziv-Aflibercept; Zaltrap (TN); VEGF Trap; VEGF Trap-Eye
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| External Link | ||||
| Regorafenib | Approved | [7] | ||
| 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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| External Link | ||||
| Bevacizumab | Approved | [8] | ||
| Synonyms |
Bevacizumab (ophthalmic slow-release tissue tablet)
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| External Link | ||||
| SYM-004 | Phase 3 | [8] | ||
| Synonyms |
Chimeric IgG1 antibody 1024 (cancer), Symphogen; Chimeric IgG1 antibody 992 (cancer), Symphogen; Chimeric IgG1 antibodies992 + 1024 (cancer), Symphogen
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| External Link | ||||
| Bevacizumab + Erlotinib | Phase 3 | [9] | ||
| External Link | ||||
| CPI-613 | Phase 3 | [8] | ||
| 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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| External Link | ||||
| Bevacizumab | Approved | [6] | ||
| External Link | ||||
| AlloStim | Phase 2/3 | [10] | ||
| Synonyms |
AlloStim (TN)
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| External Link | ||||
| Sibrotuzumab | Phase 2 | [11] | ||
| External Link | ||||
| CV301 | Phase 2 | [12] | ||
| External Link | ||||
| Efatutazone | Phase 2 | [13] | ||
| 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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| External Link | ||||
| LOR-2040 | Phase 2 | [14] | ||
| External Link | ||||
| RG7221 | Phase 2 | [15] | ||
| External Link | ||||
| PEG-SN38 | Phase 2 | [16] | ||
| Synonyms |
EZN-2208
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| External Link | ||||
| MEGF0444A | Phase 2 | [17] | ||
| External Link | ||||
| Encapsulated cell therapy | Phase 1/2 | [18] | ||
| External Link | ||||
| AB928 | Phase 1/2 | [19] | ||
| External Link | ||||
| MGD007 | Phase 1 | [15] | ||
| External Link | ||||
| BNC-101 | Phase 1 | [20] | ||
| External Link | ||||
| Navicixizumab | Phase 1 | [8] | ||
| External Link | ||||
| RG7160 | Discontinued in Phase 2 | [21] | ||
| External Link | ||||
| Nimesulide | Terminated | [22] | ||
| 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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| External Link | ||||
| Saracatinib | Phase 2 | [23] | ||
| External Link | ||||
| G3139 + Irinotecan | Investigative | [24] | ||
| External Link | ||||
References
: m6A sites