A patent review of PRMT5 inhibitors to treat cancer (2018-present)

被引:7
|
作者
Gao, Jing [1 ]
Yang, Jie [1 ]
Xue, Shengyu [2 ,3 ]
Ding, Hong [3 ]
Lin, Hua [1 ]
Luo, Cheng [2 ,3 ,4 ,5 ]
机构
[1] Fujian Normal Univ, Coll Life Sci, Biomed Res Ctr South China, Fuzhou 350117, Peoples R China
[2] Nanjing Univ Chinese Med, Sch Chinese Mat Med, Nanjing, Peoples R China
[3] Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai, Peoples R China
[4] Chinese Acad Sci, Shanghai Inst Mat Med, Zhongshan Inst Drug Discovery, Zhongshan, Peoples R China
[5] Univ Chinese Acad Sci, Sch Pharmaceut Sci & Technol, Hangzhou Inst Adv Study, Hangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
PRMT5; inhibitor; epigenetic target; cancer treatment; combined treatment; METHYLTRANSFERASE; 5; PRMT5; PROTEIN ARGININE METHYLTRANSFERASES; SYMMETRIC DIMETHYLATION; METHYLATION; DISCOVERY; OPPORTUNITIES; DEGRADATION; METHYLOSOME; TARGET; GROWTH;
D O I
10.1080/13543776.2023.2201436
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
IntroductionProtein arginine methyltransferase 5 (PRMT5) belongs to type II arginine methyltransferases. Since PRMT5 plays an essential role in mammalian cells, it can regulate various physiological functions, including cell growth and differentiation, DNA damage repair, and cell signal transduction. It is an epigenetic target with significant clinical potential and may become a powerful drug target for treating cancers and other diseases.Areas coveredThis review provides an overview of small-molecule inhibitors and their associated combined treatment strategies targeting PRMT5 in cancer treatment patents published since 2018, and also summarizes the progress made by several biopharmaceutical companies in the development, application, and clinical trials of small-molecule PRMT5 inhibitors. The data in this review come from WIPO, UniProt, PubChem, RCSB PDB, National Cancer Institute, and so on.Expert opinionMany PRMT5 inhibitors have been developed with good inhibitory activities, but most of them lack selectivities and are associated with adverse clinical responses. In addition, the progress was almost all based on the previously established skeleton, and more research and development of a new skeleton still needs to be done. The development of PRMT5 inhibitors with high activities and selectivities is still an essential aspect of research in recent years.
引用
收藏
页码:265 / 292
页数:28
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