m6A-centered Drug Response Information

General Information of the Drug (ID: M6APDG04184)
Name
CXA10
Status
Phase 2
TTD Drug ID
DF1JO7
Target Gene(s) and Their Upstream m6A Regulator, Together with the Effect of Target Gene(s) in Drug Response
The target genes involved in drug-target interaction (such as drug-metabolizing enzymes, drug transporters and therapeutic targets) and drug-mediated cell death signaling (including modulating DNA damage and repair capacity, escaping from drug-induced apoptosis, autophagy, cellular metabolic reprogramming, oncogenic bypass signaling, cell microenvironment, cell stemness, etc.) could be regulated by m6A regulator(s) and affected their corresponding drug response. You can browse detailed information on drug-related target gene(s) mediated by m6A regulators.
Cysteines of Keap1 (KEAP1 Cysteines)
Methyltransferase-like 3 (METTL3)
In total 1 mechanisms lead to this potential drug response
 Regulator Info 
Response Summary Cysteines of Keap1 (KEAP1 Cysteines) is a therapeutic target for CXA10. The Methyltransferase-like 3 (METTL3) has potential in affecting the response of CXA10 through regulating the expression of Cysteines of Keap1 (KEAP1 Cysteines). [1], [2]
YTH domain-containing family protein 1 (YTHDF1)
In total 1 mechanisms lead to this potential drug response
 Regulator Info 
Response Summary Cysteines of Keap1 (KEAP1 Cysteines) is a therapeutic target for CXA10. The YTH domain-containing family protein 1 (YTHDF1) has potential in affecting the response of CXA10 through regulating the expression of Cysteines of Keap1 (KEAP1 Cysteines). [2], [3]
Nuclear factor erythroid 2-related factor 2 (Nrf2)
Fat mass and obesity-associated protein (FTO)
In total 1 mechanisms lead to this potential drug response
 Regulator Info 
Response Summary Nuclear factor erythroid 2-related factor 2 (Nrf2) is a therapeutic target for CXA10. The Fat mass and obesity-associated protein (FTO) has potential in affecting the response of CXA10 through regulating the expression of Nuclear factor erythroid 2-related factor 2 (Nrf2). [2], [4]
Methyltransferase-like 3 (METTL3)
In total 1 mechanisms lead to this potential drug response
 Regulator Info 
Response Summary Nuclear factor erythroid 2-related factor 2 (Nrf2) is a therapeutic target for CXA10. The Methyltransferase-like 3 (METTL3) has potential in affecting the response of CXA10 through regulating the expression of Nuclear factor erythroid 2-related factor 2 (Nrf2). [1], [2]
YTH domain-containing family protein 1 (YTHDF1)
In total 1 mechanisms lead to this potential drug response
 Regulator Info 
Response Summary Nuclear factor erythroid 2-related factor 2 (Nrf2) is a therapeutic target for CXA10. The YTH domain-containing family protein 1 (YTHDF1) has potential in affecting the response of CXA10 through regulating the expression of Nuclear factor erythroid 2-related factor 2 (Nrf2). [2], [3]
YTH domain-containing protein 2 (YTHDC2)
In total 1 mechanisms lead to this potential drug response
 Regulator Info 
Response Summary Nuclear factor erythroid 2-related factor 2 (Nrf2) is a therapeutic target for CXA10. The YTH domain-containing protein 2 (YTHDC2) has potential in affecting the response of CXA10 through regulating the expression of Nuclear factor erythroid 2-related factor 2 (Nrf2). [2], [4]
References
Ref 1 METTL3-mediated M6A methylation modification is involved in colistin-induced nephrotoxicity through apoptosis mediated by Keap1/Nrf2 signaling pathway. Toxicology. 2021 Oct;462:152961. doi: 10.1016/j.tox.2021.152961. Epub 2021 Sep 21.
Ref 2 Recent progress in the development of small molecule Nrf2 modulators: a patent review (2012-2016). Expert Opin Ther Pat. 2017 Jul;27(7):763-785. doi: 10.1080/13543776.2017.1325464. Epub 2017 May 10.
Ref 3 YTHDF1 links hypoxia adaptation and non-small cell lung cancer progression. Nat Commun. 2019 Oct 25;10(1):4892. doi: 10.1038/s41467-019-12801-6.
Ref 4 Increased m6A RNA modification is related to the inhibition of the Nrf2-mediated antioxidant response in di-(2-ethylhexyl) phthalate-induced prepubertal testicular injury. Environ Pollut. 2020 Apr;259:113911. doi: 10.1016/j.envpol.2020.113911. Epub 2020 Jan 6.