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靶向核受体结合 SET 域蛋白 2(NSD2)的药物发现。

Drug Discovery Targeting Nuclear Receptor Binding SET Domain Protein 2 (NSD2).

机构信息

Chemical Biology Program, Department of Pharmacology and Toxicology, University of Texas Medical Branch (UTMB), Galveston, Texas 77555, United States.

出版信息

J Med Chem. 2023 Aug 24;66(16):10991-11026. doi: 10.1021/acs.jmedchem.3c00948. Epub 2023 Aug 14.

Abstract

Nuclear receptor binding SET domain proteins (NSDs) catalyze the mono- or dimethylation of histone 3 lysine 36 (H3K36me1 and H3K36me2), using -adenosyl-l-methionine (SAM) as a methyl donor. As a key member of the NSD family of proteins, NSD2 plays an important role in the pathogenesis and progression of various diseases such as cancers, inflammations, and infectious diseases, serving as a promising drug target. Developing potent and specific NSD2 inhibitors may provide potential novel therapeutics. Several NSD2 inhibitors and degraders have been discovered while remaining in the early stage of drug development. Excitingly, KTX-1001, a selective NSD2 inhibitor, has entered clinical trials. In this Perspective, the structures and functions of NSD2, its roles in various human diseases, and the recent advances in drug discovery strategies targeting NSD2 have been summarized. The challenges, opportunities, and future directions for developing NSD2 inhibitors and degraders are also discussed.

摘要

核受体结合 SET 域蛋白(NSDs)利用 - 腺苷甲硫氨酸(SAM)作为甲基供体,催化组蛋白 3 赖氨酸 36(H3K36me1 和 H3K36me2)的单甲基化或二甲基化。作为 NSD 家族蛋白的重要成员,NSD2 在癌症、炎症和传染病等多种疾病的发病机制和进展中发挥着重要作用,是一种很有前途的药物靶点。开发有效的、特异性的 NSD2 抑制剂可能为提供潜在的新型治疗方法。尽管处于药物开发的早期阶段,但已经发现了几种 NSD2 抑制剂和降解剂。令人兴奋的是,选择性 NSD2 抑制剂 KTX-1001 已进入临床试验阶段。在本观点中,总结了 NSD2 的结构和功能、它在各种人类疾病中的作用,以及靶向 NSD2 的药物发现策略的最新进展。还讨论了开发 NSD2 抑制剂和降解剂的挑战、机遇和未来方向。

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