Amgen Research, Amgen Inc., Thousand Oaks, CA 91320, USA.
Biochemical and Cellular Pharmacology, Genentech Inc., South San Francisco, CA 94080, USA.
Molecules. 2020 Feb 5;25(3):671. doi: 10.3390/molecules25030671.
The proteasome is the central component of the main cellular protein degradation pathway. During the past four decades, the critical function of the proteasome in numerous physiological processes has been revealed, and proteasome activity has been linked to various human diseases. The proteasome prevents the accumulation of misfolded proteins, controls the cell cycle, and regulates the immune response, to name a few important roles for this macromolecular "machine." As a therapeutic target, proteasome inhibitors have been approved for the treatment of multiple myeloma and mantle cell lymphoma. However, inability to sufficiently inhibit proteasome activity at tolerated doses has hampered efforts to expand the scope of proteasome inhibitor-based therapies. With emerging new modalities in myeloma, it might seem challenging to develop additional proteasome-based therapies. However, the constant development of new applications for proteasome inhibitors and deeper insights into the intricacies of protein homeostasis suggest that proteasome inhibitors might have novel therapeutic applications. Herein, we summarize the latest advances in proteasome inhibitor development and discuss the future of proteasome inhibitors and other proteasome-based therapies in combating human diseases.
蛋白酶体是主要细胞蛋白降解途径的核心组成部分。在过去的四十年中,蛋白酶体在许多生理过程中的关键功能已经被揭示,并且蛋白酶体的活性与各种人类疾病有关。蛋白酶体可防止错误折叠的蛋白质积累,控制细胞周期并调节免疫反应,仅举几个这个大分子“机器”的重要作用。作为一种治疗靶点,蛋白酶体抑制剂已被批准用于治疗多发性骨髓瘤和套细胞淋巴瘤。然而,由于无法在可耐受的剂量下充分抑制蛋白酶体的活性,因此限制了基于蛋白酶体抑制剂的治疗方法的扩展。随着骨髓瘤中出现新的治疗方法,似乎难以开发更多基于蛋白酶体的治疗方法。然而,蛋白酶体抑制剂新应用的不断出现以及对蛋白质动态平衡复杂性的深入了解表明,蛋白酶体抑制剂可能具有新的治疗应用。本文总结了蛋白酶体抑制剂开发的最新进展,并讨论了蛋白酶体抑制剂和其他基于蛋白酶体的治疗方法在对抗人类疾病方面的未来。