m6A-centered Crosstalk Information
Mechanism of Crosstalk between m6A Modification and Epigenetic Regulation
| Crosstalk ID |
M6ACROT05537
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[1] | |||
m6A modification
ZFAS1
ZFAS1
IMP2
: m6A sites
Direct
Enhancement
Non-coding RNA
ZFAS1
OLA1
lncRNA miRNA circRNA
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| m6A Modification: | |||||
|---|---|---|---|---|---|
| m6A Regulator | Insulin-like growth factor 2 mRNA-binding protein 2 (IGF2BP2) | READER | |||
| m6A Target | ZNFX1 antisense RNA 1 (ZFAS1) | ||||
| Epigenetic Regulation that have Cross-talk with This m6A Modification: | |||||
| Epigenetic Regulation Type | Non-coding RNA (ncRNA) | ||||
| Epigenetic Regulator | ZNFX1 antisense RNA 1 (ZFAS1) | LncRNA | View Details | ||
| Regulated Target | Obg-like ATPase 1 (OLA1) | View Details | |||
| Crosstalk Relationship | m6A → ncRNA | Enhancement | |||
| Crosstalk Mechanism | m6A regulators directly modulate the functionality of ncRNAs through specific targeting ncRNA | ||||
| Crosstalk Summary | The critical modulation network underlying m6A readers stabilizes lncRNAs, and they jointly promote mitochondrial energy metabolism in the pathogenesis of colorectal cancer. N6-methyladenosine reader stabilizes the ZNFX1 antisense RNA 1 (ZFAS1)/Obg-like ATPase 1 (OLA1) axis. Thus, direct interaction between the KH3-4 domain of IMP2 and ZFAS1 where IMP2 serves as a reader for m6A-modified ZFAS1 and promotes the RNA stability of ZFAS1 is critical for CRC development. | ||||
| Responsed Disease | Colorectal cancer | ICD-11: 2B91 | |||
| Cell Process | Cell proliferation | ||||
| Cell colony formation | |||||
| Cell apoptosis | |||||
In-vitro Model |
SW480 | Colon adenocarcinoma | Homo sapiens | CVCL_0546 | |
| SW620 | Colon adenocarcinoma | Homo sapiens | CVCL_0547 | ||
| HCT 116 | Colon carcinoma | Homo sapiens | CVCL_0291 | ||
| SW48 | Colon adenocarcinoma | Homo sapiens | CVCL_1724 | ||
| RKO | Colon carcinoma | Homo sapiens | CVCL_0504 | ||
| Caco-2 | Colon adenocarcinoma | Homo sapiens | CVCL_0025 | ||
| LoVo | Colon adenocarcinoma | Homo sapiens | CVCL_0399 | ||
| HT-29 | Colon adenocarcinoma | Homo sapiens | CVCL_0320 | ||
| In-vivo Model | The 4-week-old BALB/c-nu mice (half of the female and half of the male),They were randomized into groups with approximately equivalent numbers before tumor cell inoculation. The investigator was blinded to the group allocation of the animals during the experiment; 5 × 106 HCT116 cells were injected subcutaneously into the right armpit region. | ||||
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 | ||
| Retifanlimab | Approved | [2] | ||
| Synonyms |
INCMGA0012; Retifanlimab
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| External Link | ||||
| Aflibercept | Approved | [3] | ||
| Synonyms |
Ziv-Aflibercept; Zaltrap (TN); VEGF Trap; VEGF Trap-Eye
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| External Link | ||||
| 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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| Bevacizumab | Approved | [5] | ||
| Synonyms |
Bevacizumab (ophthalmic slow-release tissue tablet)
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| External Link | ||||
| 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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| Bevacizumab + Erlotinib | Phase 3 | [6] | ||
| External Link | ||||
| 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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| External Link | ||||
| Bevacizumab | Approved | [3] | ||
| External Link | ||||
| AlloStim | Phase 2/3 | [7] | ||
| Synonyms |
AlloStim (TN)
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| External Link | ||||
| Sibrotuzumab | Phase 2 | [8] | ||
| External Link | ||||
| CV301 | Phase 2 | [9] | ||
| External Link | ||||
| 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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| External Link | ||||
| LOR-2040 | Phase 2 | [11] | ||
| External Link | ||||
| RG7221 | Phase 2 | [12] | ||
| External Link | ||||
| PEG-SN38 | Phase 2 | [13] | ||
| Synonyms |
EZN-2208
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| External Link | ||||
| MEGF0444A | Phase 2 | [14] | ||
| External Link | ||||
| Encapsulated cell therapy | Phase 1/2 | [15] | ||
| External Link | ||||
| AB928 | Phase 1/2 | [16] | ||
| External Link | ||||
| MGD007 | Phase 1 | [12] | ||
| External Link | ||||
| BNC-101 | Phase 1 | [17] | ||
| External Link | ||||
| Navicixizumab | Phase 1 | [5] | ||
| External Link | ||||
| RG7160 | Discontinued in Phase 2 | [18] | ||
| External Link | ||||
| 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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| External Link | ||||
| Saracatinib | Phase 2 | [20] | ||
| External Link | ||||
| G3139 + Irinotecan | Investigative | [21] | ||
| External Link | ||||
References
: m6A sites