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Title:
m6A writer WTAP targets NRF2 to accelerate bladder cancer malignancy via m6A-dependent ferroptosis regulation | Apoptosis
Description:
Recent evidence have indicated that ferroptosis, a novel iron-dependent form of non-apoptotic cell death, plays a critical role in human cancers. Besides, emerging literatures have revealed the ovel function of N6-methyladenosine (m6A) in bladder cancer physiological. However, the underlying mechanism of m6A on bladder cancer is still unclear. Here, present work revealed that m6A methyltransferase (āwriterā) WTAP up-regulated in bladder cancer tissue and cells, indicating the poor prognosis of bladder cancer patients. Functionally, gain/loss-of-functional experiments illustrated that WTAP promoted the viability of bladder cancer cells and inhibited the erastin-induced ferroptosis. Mechanistically, there was a remarkable m6A modification site on 3ā-UTR of endogenous antioxidant factor NRF2 RNA and WTAP could install its methylation. Moreover, m6A reader YTHDF1 recognized the m6A site on NRF2 mRNA and enhanced its mRNA stability. Therefore, these findings demonstrated potential therapeutic strategyies for bladder cancer via m6A-dependent manner.
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Keywords {š}
article, cancer, pubmed, google, scholar, bladder, wang, cas, ferroptosis, central, cell, zhang, gang, death, nmethyladenosine, mol, wtap, nrf, chen, yang, access, privacy, cookies, content, information, madependent, liang, modification, liu, shaanxi, china, springer, supplementary, material, data, publish, search, manuscript, lin, rna, manner, tang, author, authors, xian, hospital, nature, site, function, log,
Topics {āļø}
month download article/chapter fto/mir-576/cdk6 axis rna n6-methyladenosine modifications autophagy-mediated gpx4 degradation m6a-dependent ferroptosis regulation article apoptosis aims electronic supplementary material nrf2-modulated genes full article pdf m6a rna methylation m6a-dependent manner n6-methyladenosine modification holds exclusive rights privacy choices/manage cookies a-dependent manner bladder cancer physiological bladder cancer tissue bladder cancer patients bladder cancer males bladder cancer cells ferroptosis-related genes related subjects methyltransferase kiaa1429 acts references dobruch main manuscript text apoptotic cell death programmed cell death european economic area functional experiments illustrated digestive system malignancies peripheral blood leukocytes ethics declarations conflict accepted manuscript version iron-dependent form m6a modification conditions privacy policy erastin-induced ferroptosis fin56-induced ferroptosis article wang article log personal data biomedical information engineering additional information publisher accepting optional cookies yarong wang wrote bladder cancer human cancers urological cancers neurological diseases article cite
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headline:m6A writer WTAP targets NRF2 to accelerate bladder cancer malignancy via m6A-dependent ferroptosis regulation
description:Recent evidence have indicated that ferroptosis, a novel iron-dependent form of non-apoptotic cell death, plays a critical role in human cancers. Besides, emerging literatures have revealed the ovel function of N6-methyladenosine (m6A) in bladder cancer physiological. However, the underlying mechanism of m6A on bladder cancer is still unclear. Here, present work revealed that m6A methyltransferase (āwriterā) WTAP up-regulated in bladder cancer tissue and cells, indicating the poor prognosis of bladder cancer patients. Functionally, gain/loss-of-functional experiments illustrated that WTAP promoted the viability of bladder cancer cells and inhibited the erastin-induced ferroptosis. Mechanistically, there was a remarkable m6A modification site on 3ā-UTR of endogenous antioxidant factor NRF2 RNA and WTAP could install its methylation. Moreover, m6A reader YTHDF1 recognized the m6A site on NRF2 mRNA and enhanced its mRNA stability. Therefore, these findings demonstrated potential therapeutic strategyies for bladder cancer via m6A-dependent manner.
datePublished:2023-01-31T00:00:00Z
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WTAP
Ferroptosis
Bladder cancer
NRF2.
Cancer Research
Cell Biology
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Biochemistry
general
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headline:m6A writer WTAP targets NRF2 to accelerate bladder cancer malignancy via m6A-dependent ferroptosis regulation
description:Recent evidence have indicated that ferroptosis, a novel iron-dependent form of non-apoptotic cell death, plays a critical role in human cancers. Besides, emerging literatures have revealed the ovel function of N6-methyladenosine (m6A) in bladder cancer physiological. However, the underlying mechanism of m6A on bladder cancer is still unclear. Here, present work revealed that m6A methyltransferase (āwriterā) WTAP up-regulated in bladder cancer tissue and cells, indicating the poor prognosis of bladder cancer patients. Functionally, gain/loss-of-functional experiments illustrated that WTAP promoted the viability of bladder cancer cells and inhibited the erastin-induced ferroptosis. Mechanistically, there was a remarkable m6A modification site on 3ā-UTR of endogenous antioxidant factor NRF2 RNA and WTAP could install its methylation. Moreover, m6A reader YTHDF1 recognized the m6A site on NRF2 mRNA and enhanced its mRNA stability. Therefore, these findings demonstrated potential therapeutic strategyies for bladder cancer via m6A-dependent manner.
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WTAP
Ferroptosis
Bladder cancer
NRF2.
Cancer Research
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Biochemistry
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