4.7 Review

N-6-Methyladenosine modification: a novel pharmacological target for anti-cancer drug development

期刊

ACTA PHARMACEUTICA SINICA B
卷 8, 期 6, 页码 833-843

出版社

INST MATERIA MEDICA, CHINESE ACAD MEDICAL SCIENCES
DOI: 10.1016/j.apsb.2018.06.001

关键词

N-6-Methyladenosine; Human cancer; Pharmacological target; m(6)A modification regulator; Drug development

资金

  1. National Natural Science Foundation of China [31701114]
  2. National for University-Key Cultivation Project of Young Teacher in Sun Yat-Sen University [17ykzd11]

向作者/读者索取更多资源

N-6-Methyladenosine (m(6)A) modification is the most pervasive modification of human mRNA molecules. It is reversible via regulation of m(6)A modification methyltransferase, demethylase and proteins that preferentially recognize m(6)A modification as writers, erasers and readers, respectively. Altered expression levels of the m(6)A modification key regulators substantially affect their function, leading to significant phenotype changes in the cell and organism. Recent studies have proved that the m(6)A modification plays significant roles in regulation of metabolism, stem cell self-renewal, and metastasis in a variety of human cancers. In this review, we describe the potential roles of m(6)A modification in human cancers and summarize their underlying molecular mechanisms. Moreover, we will highlight potential therapeutic approaches by targeting the key m(6)A modification regulators for cancer drug development. (C) 2018 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据