m6A-centered Crosstalk Information
Mechanism of Crosstalk between m6A Modification and Epigenetic Regulation
| Crosstalk ID |
M6ACROT05488
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[1] | |||
m6A modification
Circ_1662
Circ_1662
METTL3
Methylation
: m6A sites
Direct
Enhancement
Non-coding RNA
circ1662
YAP1
lncRNA miRNA circRNA
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| m6A Modification: | |||||
|---|---|---|---|---|---|
| m6A Regulator | Methyltransferase-like 3 (METTL3) | WRITER | |||
| m6A Target | Circ_1662 | ||||
| Epigenetic Regulation that have Cross-talk with This m6A Modification: | |||||
| Epigenetic Regulation Type | Non-coding RNA (ncRNA) | ||||
| Epigenetic Regulator | Circ_1662 | circRNA | View Details | ||
| Regulated Target | Transcriptional coactivator YAP1 (YAP1) | View Details | |||
| Crosstalk Relationship | m6A → ncRNA | Enhancement | |||
| Crosstalk Mechanism | m6A regulators directly modulate the functionality of ncRNAs through specific targeting ncRNA | ||||
| Crosstalk Summary | METTL3-induced Circ_1662 promoted colorectal cancer cell invasion and migration by accelerating Transcriptional coactivator YAP1 (YAP1) nuclear transport. Circ1662 enhanced CRC invasion and migration depending on YAP1 and SMAD3. This result implies that circ1662 is a new prognostic and therapeutic marker for CRC metastasis. | ||||
| Responsed Disease | Colorectal cancer | ICD-11: 2B91 | |||
| Cell Process | Cell invasion | ||||
| Cell migration | |||||
| Epithelial-mesenchymal transition | |||||
In-vitro Model |
HCT 116 | Colon carcinoma | Homo sapiens | CVCL_0291 | |
| SW480 | Colon adenocarcinoma | Homo sapiens | CVCL_0546 | ||
| HEK293T | Normal | Homo sapiens | CVCL_0063 | ||
| In-vivo Model | BALB/c nude mice (4 weeks old) were acquired from Vital River Laboratory (Beijing, China). HCT116 cells with stable circ1662 expression (2 × 106 in 100 L of PBS) were injected via the tail vein. After 45 days, the mice were sacrificed. The lung metastatic carcinoma specimens were processed into paraffin-embedded sections for subsequent H&E staining and IHC. | ||||
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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| Aflibercept | Approved | [3] | ||
| Synonyms |
Ziv-Aflibercept; Zaltrap (TN); VEGF Trap; VEGF Trap-Eye
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| 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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| Bevacizumab | Approved | [3] | ||
| External Link | ||||
| AlloStim | Phase 2/3 | [7] | ||
| Synonyms |
AlloStim (TN)
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| 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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| 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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| 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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| Saracatinib | Phase 2 | [20] | ||
| External Link | ||||
| G3139 + Irinotecan | Investigative | [21] | ||
| External Link | ||||
References
: m6A sites