RNA甲基化
N6-甲基腺苷
甲基化
甲基转移酶
核糖核酸
生物
癌变
表观遗传学
癌症研究
计算生物学
遗传学
癌症
基因
作者
Zhaolin Chen,Ying Hu,Le Jin,Fan Yang,Haiwen Ding,Lei Zhang,Lili Li,Tingting Pan
标识
DOI:10.3389/fphar.2022.873030
摘要
N6-methyladenosine (m6A) RNA methylation has been considered the most prevalent, abundant, and conserved internal transcriptional modification throughout the eukaryotic mRNAs. Typically, m6A RNA methylation is catalyzed by the RNA methyltransferases (writers), is removed by its demethylases (erasers), and interacts with m6A-binding proteins (readers). Accumulating evidence shows that abnormal changes in the m6A levels of these regulators are increasingly associated with human tumorigenesis and drug resistance. However, the molecular mechanisms underlying m6A RNA methylation in tumor occurrence and development have not been comprehensively clarified. We reviewed the recent findings on biological regulation of m6A RNA methylation and summarized its potential therapeutic strategies in various human cancers.
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