Protein Arginine Methyltransferase 5 (PRMT5) as an Anticancer Target and Its Inhibitor Discovery

被引:89
|
作者
Wang, Yuanxiang [1 ]
Hu, Wenhao [1 ]
Yuan, Yanqiu [1 ]
机构
[1] Sun Yat Sen Univ, Sch Pharmaceut Sci, Guangzhou 510006, Guangdong, Peoples R China
关键词
SELECTIVE INHIBITORS; KINETIC MECHANISM; SM PROTEINS; METHYLATION; BINDING; GROWTH; EXPRESSION; RESIDUES; REPEAT; POTENT;
D O I
10.1021/acs.jmedchem.8b00598
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
PRA/ITS is a major enzyme responsible for symmetric dimethylation of arginine residues on both histone and non-histone proteins, regulating many biological pathways in mammalian cells. PRMT5 has been suggested as a therapeutic target in a variety of diseases including infectious disease, heart disease, and cancer. Many PRMT5 inhibitors have been discovered in the past 5 years, and one entered clinical trial in 2015 for the treatment of solid tumor and mantle cell lymphoma (MCL). The aim of this review is to summarize the current understanding of the roles of PRA/ITS in cancer and the discovery of PRMT5 enzymatic inhibitors. By reviewing the structure-activity relationship (SAR) of known inhibitors of PRMT5, we hope to provide guidance for future drug designs and inhibitor optimization. Opportunities and limitations of PRMT5 inhibitors for the treatment are also discussed.
引用
收藏
页码:9429 / 9441
页数:13
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