Kisselev Alexei F, van der Linden Wouter A, Overkleeft Herman S
Department of Pharmacology and Toxicology, Norris Cotton Cancer Center, Dartmouth Medical School, Lebanon, NH 03756, USA.
Chem Biol. 2012 Jan 27;19(1):99-115. doi: 10.1016/j.chembiol.2012.01.003.
Proteasomes are large, multisubunit proteolytic complexes presenting multiple targets for therapeutic intervention. The 26S proteasome consists of a 20S proteolytic core and one or two 19S regulatory particles. The 20S core contains three types of active sites. Many structurally diverse inhibitors of these active sites, both natural product and synthetic, have been discovered in the last two decades. One, bortezomib, is used clinically for treatment of multiple myeloma, mantle cell lymphoma, and acute allograft rejection. Five more recently developed proteasome inhibitors are in trials for treatment of myeloma and other cancers. Proteasome inhibitors also have activity in animal models of autoimmune and inflammatory diseases, reperfusion injury, promote bone and hair growth, and can potentially be used as anti-infectives. In addition, inhibitors of ATPases and deubiquitinases of 19S regulatory particles have been discovered in the last decade.
蛋白酶体是大型多亚基蛋白水解复合物,为治疗干预提供了多个靶点。26S蛋白酶体由一个20S蛋白水解核心和一个或两个19S调节颗粒组成。20S核心包含三种类型的活性位点。在过去二十年中,已经发现了许多结构多样的这些活性位点抑制剂,包括天然产物和合成抑制剂。其中一种,硼替佐米,临床上用于治疗多发性骨髓瘤、套细胞淋巴瘤和急性移植物排斥反应。另外五种最近开发的蛋白酶体抑制剂正在进行治疗骨髓瘤和其他癌症的试验。蛋白酶体抑制剂在自身免疫性和炎性疾病、再灌注损伤的动物模型中也具有活性,可促进骨骼和毛发的生长,并且有可能用作抗感染药。此外,在过去十年中还发现了19S调节颗粒的ATP酶和去泛素酶抑制剂。