Balance-Based Drug Discovery Laboratory, School of Pharmaceutical Sciences, Sun Yat-Sen University, Guangzhou 510006, China.
J Med Chem. 2023 Jul 13;66(13):8407-8427. doi: 10.1021/acs.jmedchem.3c00250. Epub 2023 Jun 27.
As a predominant type II protein arginine methyltransferase, PRMT5 plays critical roles in various normal cellular processes by catalyzing the mono- and symmetrical dimethylation of a wide range of histone and nonhistone substrates. Clinical studies have revealed that high expression of PRMT5 is observed in different solid tumors and hematological malignancies and is closely associated with cancer initiation and progression. Accordingly, PRMT5 is becoming a promising anticancer target and has received great attention in both the pharmaceutical industry and the academic community. In this Perspective, we comprehensively summarize recent advances in the development of first-generation PRMT5 enzymatic inhibitors and highlight novel strategies targeting PRMT5 in the past 5 years. We also discuss the challenges and opportunities of PRMT5 inhibition, with the aim of shedding light on future PRMT5 drug discovery.
作为主要的 II 型蛋白精氨酸甲基转移酶,PRMT5 通过催化广泛的组蛋白和非组蛋白底物的单甲基化和对称二甲基化,在各种正常细胞过程中发挥关键作用。临床研究表明,PRMT5 在不同的实体瘤和血液恶性肿瘤中高表达,与癌症的发生和发展密切相关。因此,PRMT5 正在成为一个有前途的抗癌靶点,在制药行业和学术界都受到了极大的关注。在本观点中,我们全面总结了第一代 PRMT5 酶抑制剂开发的最新进展,并重点介绍了过去 5 年中靶向 PRMT5 的新策略。我们还讨论了 PRMT5 抑制的挑战和机遇,旨在为未来的 PRMT5 药物发现提供思路。