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      SETD2 as a regulator of N6-methyladenosine RNA methylation and modifiers in cancer.

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          Abstract

          Cancer is an unpleasant, painful disease. It is one of the most devastating diseases worldwide diminishing many lives. Many genetic and epigenetic changes occur before cancer develops. Mutation in SETD2 gene is one such example. RNA splicing, DNA damage repair, DNA methylation and histone methylation are some of the biological processes mediated by SETD2. SETD2 (histone H3 lysine 36 methyltransferase) is a frequently mutated gene in different types of cancer. Loss of SETD2 is associated with worse prognosis and aggressive phenotypes. Histone modification is one of the epigenetic regulation having a significant effect on gene regulation. N6-methyladenosine (m6A) mRNA modification is a well-known posttranscriptional modification playing a pivotal role in many normal and pathological processes affecting RNA metabolism. SETD2 catalyses H3K36 trimethylation and in turn H3K36me3 guides the deposition of m6A on nascent RNA transcripts. Finally, this review summarizes the deep understanding of the role of SETD2 in RNA methylation/modification and how SETD2 mutation contributes to tumour development.

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          Author and article information

          Journal
          Eur J Cancer Prev
          European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP)
          Ovid Technologies (Wolters Kluwer Health)
          1473-5709
          0959-8278
          November 2020
          : 29
          : 6
          Affiliations
          [1 ] Department of Life Science, National Institute of Technology, Rourkela, India.
          Article
          00008469-202011000-00013
          10.1097/CEJ.0000000000000587
          33021769
          0b9eee07-0722-4c5f-833e-3bf272bb3043
          History

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