| Literature DB >> 28867248 |
Siwei Wang1, Chunxiao Sun2, Jianhua Li3, Erbao Zhang4, Zhifei Ma1, Weizhang Xu1, Hong Li2, Mantang Qiu5, Youtao Xu6, Wenjia Xia6, Lin Xu7, Rong Yin8.
Abstract
Reversible methylation by means of N6-methyladenosine (m6A) is the most prevalent internal modification in mammalian mRNA. This RNA chemical mark is created by proteins that are m6A "writers" and can be reversed by proteins that are m6A "erasers" (i.e., demethylases). Some other proteins serving as "readers" can recognize m6A-containing mRNA and regulate downstream molecular mechanisms accordingly. Although m6A bases in RNA perform critical functions in important biological processes, their roles in cancer biology and cancer stem cells remain largely unknown. In this review, we focus on the m6A-associated mechanisms and modification landscapes in several major malignant tumors. Global and detailed analyses were both conducted on relevant high-throughput sequencing data. Possible interventions against m6A demethylases are also explored in this review, which may be advantageous for the treatment of m6A related cancers.Entities:
Keywords: Cancer therapy; Human cancers; N6-methyladenosine; RNA methylation; m(6)A
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Year: 2017 PMID: 28867248 DOI: 10.1016/j.canlet.2017.08.030
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679