Mission Therapeutics Ltd, Moneta, Babraham Research Campus, Cambridge CB22 3AT, UK.
Artios Pharmaceuticals Ltd, Maia, Babraham Research Campus, Cambridge CB22 3AT, UK.
Nat Rev Drug Discov. 2018 Jan;17(1):57-78. doi: 10.1038/nrd.2017.152. Epub 2017 Sep 29.
More than a decade after a Nobel Prize was awarded for the discovery of the ubiquitin-proteasome system and clinical approval of proteasome and ubiquitin E3 ligase inhibitors, first-generation deubiquitylating enzyme (DUB) inhibitors are now approaching clinical trials. However, although our knowledge of the physiological and pathophysiological roles of DUBs has evolved tremendously, the clinical development of selective DUB inhibitors has been challenging. In this Review, we discuss these issues and highlight recent advances in our understanding of DUB enzymology and biology as well as technological improvements that have contributed to the current interest in DUBs as therapeutic targets in diseases ranging from oncology to neurodegeneration.
在因发现泛素-蛋白酶体系统而获得诺贝尔奖以及蛋白酶体和泛素 E3 连接酶抑制剂获得临床批准十多年后,第一代去泛素化酶 (DUB) 抑制剂现已进入临床试验阶段。然而,尽管我们对 DUB 的生理和病理生理作用的了解已经有了巨大的发展,但选择性 DUB 抑制剂的临床开发一直具有挑战性。在这篇综述中,我们讨论了这些问题,并强调了我们在 DUB 酶学和生物学方面的理解以及技术改进方面的最新进展,这些进展促成了目前人们对 DUB 作为从肿瘤学到神经退行性疾病等疾病的治疗靶点的兴趣。