Inhibitors of Protein Methyltransferases and Demethylases

被引:218
|
作者
Kaniskan, H. Umit [1 ]
Martini, Michael L.
Jin, Jian [1 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Pharmacol Sci, New York, NY 10029 USA
基金
美国国家卫生研究院;
关键词
SMALL-MOLECULE INHIBITORS; NF-KAPPA-B; LINKED MENTAL-RETARDATION; LSD1 HISTONE DEMETHYLASE; ACUTE MYELOID-LEUKEMIA; REPRESSIVE COMPLEX 2; HUMAN CANCER-CELLS; H3; LYSINE-4; METHYLTRANSFERASE; STRUCTURE-BASED OPTIMIZATION; MECHANISM-BASED INACTIVATOR;
D O I
10.1021/acs.chemrev.6b00801
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Post-translational modifications of histones by protein methyltransferases (PMTs) and histone demethylases (KDMs) play an important role in the regulation of gene expression and transcription and are implicated in cancer and many other diseases. Many of these enzymes also target various nonhistone proteins impacting numerous crucial biological pathways. Given their key biological functions and implications in human diseases, there has been a growing interest in assessing these enzymes as potential therapeutic targets. Consequently, discovering and developing inhibitors of these enzymes has become a very active and fast-growing research area over the past decade. In this review, we cover the discovery, characterization, and biological application of inhibitors of PMTs and KDMs with emphasis on key advancements in the field. We also discuss challenges, opportunities, and future directions in this emerging, exciting research field.
引用
收藏
页码:989 / 1068
页数:80
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