Selective Inhibitors of Protein Methyltransferases

被引:115
作者
Kaniskan, H. Uemit [1 ]
Konze, Kyle D. [1 ]
Jin, Jian [1 ,2 ,3 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Struct & Chem Biol, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Dept Oncol Sci, New York, NY 10029 USA
[3] Icahn Sch Med Mt Sinai, Dept Pharmacol & Syst Therapeut, New York, NY 10029 USA
基金
美国国家卫生研究院;
关键词
SMALL-MOLECULE INHIBITORS; EZH2 HISTONE METHYLTRANSFERASE; SET DOMAIN PROTEINS; ARGININE-METHYLTRANSFERASE; LYSINE METHYLTRANSFERASES; DNA METHYLATION; BREAST-CANCER; TRANSCRIPTIONAL ACTIVATION; CHEMICAL PROBE; IN-VIVO;
D O I
10.1021/jm501234a
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Mounting evidence suggests that protein methyltransferases (PMTs), which catalyze methylation of histone and nonhistone proteins, play a crucial role in diverse biological processes and human diseases. In particular, PMTs have been recognized as major players in regulating gene expression and chromatin state. PMTs are divided into two categories: protein lysine methyltransferases (PKMTs) and protein arginine methyltransferases (PRMTs). There has been a steadily growing interest in these enzymes as potential therapeutic targets and therefore discovery of PMT inhibitors has also been pursued increasingly over the past decade. Here, we present a perspective on selective, small-molecule inhibitors of PMTs with an emphasis on their discovery, characterization, and applicability as chemical tools for deciphering the target PMTs physiological functions and involvement in human diseases. We highlight the current state of PMT inhibitors and discuss future directions and opportunities for PMT inhibitor discovery.
引用
收藏
页码:1596 / 1629
页数:34
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