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去泛素化酶抑制剂的治疗潜力。

The therapeutic potential of deubiquitinating enzyme inhibitors.

机构信息

Hybrigenics SA, 3-5 Impasse Reille, 75014 Paris, France.

出版信息

Biochem Soc Trans. 2010 Feb;38(Pt 1):137-43. doi: 10.1042/BST0380137.

Abstract

Proteases play a key role in various pathological processes and several protease inhibitors are already available for treatment. DUBs (deubiquitinating enzymes) constitute one of the largest classes of human proteases and are key effectors of the ubiquitin-proteasome system. This pathway regulating cellular protein turnover has been implicated in the pathogenesis of many human diseases, including neurodegenerative disorders, viral diseases and cancer. The therapeutic efficacy of the proteasome inhibitor Velcade (bortezomib) for treating multiple myeloma and mantle cell lymphoma establishes this system as a valid target for cancer treatment. A promising alternative to targeting the proteasome itself would be to target the upstream, ubiquitin conjugation/deconjugation system, to generate more specific, less toxic anticancer agents. Advances in small molecule-based inhibitors specifically targeting DUBs are presented in this review.

摘要

蛋白酶在各种病理过程中起着关键作用,已有几种蛋白酶抑制剂可用于治疗。DUBs(去泛素化酶)是人类最大的蛋白酶类之一,是泛素-蛋白酶体系统的关键效应因子。这条调节细胞内蛋白质周转的途径与许多人类疾病的发病机制有关,包括神经退行性疾病、病毒疾病和癌症。蛋白酶体抑制剂硼替佐米(Velcade)治疗多发性骨髓瘤和套细胞淋巴瘤的疗效证实了该系统是癌症治疗的有效靶点。与针对蛋白酶体本身相比,针对上游泛素缀合/去缀合系统可能是一种更有前途的方法,可以产生更特异、毒性更小的抗癌药物。本文综述了针对 DUB 的小分子抑制剂的最新进展。

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