m6A-centered Crosstalk Information
Mechanism of Crosstalk between m6A Modification and Epigenetic Regulation
| Crosstalk ID |
M6ACROT03283
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[1], [2] | |||
Histone modification
H3K4me3
KDM5C
METTL14
Direct
Inhibition
m6A modification
ARRDC4
ARRDC4
METTL14
Methylation
: m6A sites
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| m6A Modification: | |||||
|---|---|---|---|---|---|
| m6A Regulator | Methyltransferase-like 14 (METTL14) | WRITER | |||
| m6A Target | Arrestin domain-containing protein 4 (ARRDC4) | ||||
| Epigenetic Regulation that have Cross-talk with This m6A Modification: | |||||
| Epigenetic Regulation Type | Histone modification (HistMod) | ||||
| Epigenetic Regulator | Lysine-specific demethylase 5C (KDM5C) | ERASER | View Details | ||
| Regulated Target | Histone H3 lysine 4 trimethylation (H3K4me3) | View Details | |||
| Downstream Gene | METTL14 | View Details | |||
| Crosstalk Relationship | Histone modification → m6A | Inhibition | |||
| Crosstalk Mechanism | histone modification directly impacts m6A modification through modulating the level of m6A regulator | ||||
| Crosstalk Summary | Both the univariate and multivariate Cox regression analysis indicated that METTL14 was an independent prognostic factor in CRC. Moreover, KDM5C-mediated demethylation of Histone H3 lysine 36 trimethylation (H3K36me3) in the promoter of METTL14 inhibited METTL14 transcription. Knockdown of METTL14 significantly enhanced Arrestin domain-containing protein 4 (ARRDC4) mRNA stability relying on the "reader" protein YHTDF2 dependent manner in colorectal cancer. | ||||
| Responsed Disease | Colorectal cancer | ICD-11: 2B91 | |||
| Pathway Response | mRNA surveillance pathway | hsa03015), RNA degradation | |||
| Cell Process | RNA stability | ||||
In-vitro Model |
NCM460 | Normal | Homo sapiens | CVCL_0460 | |
| HCT 116 | Colon carcinoma | Homo sapiens | CVCL_0291 | ||
| HCT 8 | Colon adenocarcinoma | Homo sapiens | CVCL_2478 | ||
| SW620 | Colon adenocarcinoma | Homo sapiens | CVCL_0547 | ||
| SW480 | Colon adenocarcinoma | Homo sapiens | CVCL_0546 | ||
| HT29 | Colon cancer | Mus musculus | CVCL_A8EZ | ||
| DLD-1 | Colon adenocarcinoma | Homo sapiens | CVCL_0248 | ||
| In-vivo Model | All animal experiments were approved by the animal care Committee of Nanjing First Hospital, Nanjing Medial University (acceptance No. SYXK 20160006). 2 × 106 transfected HCT116 cells in 0.2 ml PBS were injected into the tail vein of nude mice which were randomly divided into nine groups (eight mice per group). After 2 months of injection, mice were sacrificed, and their lungs were removed and stained by Hematoxylin and Eosin (HE) Staining. | ||||
Full List of Potential Compound(s) Related to This m6A-centered Crosstalk
| Lysine-specific demethylase 5C (KDM5C) | 2 Compound(s) Regulating the Target | Click to Show/Hide the Full List | ||
| PBIT | Investigative | [3] | ||
| Synonyms |
2514-30-9; 2-(4-methylphenyl)-1,2-benzisothiazol-3(2H)-one; 2-(4-methylphenyl)-1,2-benzothiazol-3-one; MLS000583746; 2-(p-Tolyl)benzo[d]isothiazol-3(2H)-one; 2-(p-tolyl)-1,2-benzothiazol-3-one; SMR000200989; 2-(4-methylphenyl)-1,2-benzothiazol-3(2H)-one; 1,2-Benzisothiazol-3(2H)-one, 2-(4-methylphenyl)-; 2-(4-methylphenyl)-2,3-dihydro-1,2-benzothiazol-3-one; ChemDiv3_007090; AC1LIP69; cid_935415; SCHEMBL2443755; GTPL7026; CHEMBL1336959; CTK0J4356; BDBM34737; AOB6896; DTXSID10359056; MolPort-002-285-696; HMS2576N21
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| MOA | Inhibitor | |||
| External Link | ||||
| IOX2 | Investigative | [4] | ||
| Synonyms |
compound 6
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| 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
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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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| 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