Moore Bradley S, Eustáquio Alessandra S, McGlinchey Ryan P
Center for Marine Biotechnology and Biomedicine, Scripps Institution of Oceanography, University of California at San Diego, La Jolla, CA 92093, USA.
Curr Opin Chem Biol. 2008 Aug;12(4):434-40. doi: 10.1016/j.cbpa.2008.06.033. Epub 2008 Jul 24.
With the recent US Food and Drug Administration approval of bortezomib (Velcade) for the treatment of relapsed multiple myeloma, the proteasome has emerged as a new therapeutic target with diverse pathology. Drug discovery programs in academia and the pharmaceutical industry have developed a range of low nanomolar synthetic and natural inhibitors of the 20S proteasome core particle that have entered human clinical trials as significant anti-cancer and anti-inflammatory leads. Moreover, proteasome inhibitors continue to serve as valuable research tools in cellular biology through the elucidation of important biological processes associated with the ubiquitin-proteasome pathway of protein degradation. This review will highlight recent advances in the development and application of proteasome inhibitors.
随着美国食品药品监督管理局最近批准硼替佐米(万珂)用于治疗复发的多发性骨髓瘤,蛋白酶体已成为一个具有多种病理情况的新治疗靶点。学术界和制药行业的药物研发项目已开发出一系列低纳摩尔浓度的20S蛋白酶体核心颗粒的合成和天然抑制剂,这些抑制剂已作为重要的抗癌和抗炎先导药物进入人体临床试验。此外,蛋白酶体抑制剂通过阐明与蛋白质降解的泛素-蛋白酶体途径相关的重要生物学过程,继续作为细胞生物学中有价值的研究工具。本综述将重点介绍蛋白酶体抑制剂开发和应用方面的最新进展。