Targeting the Ubiquitin–Proteasome System for Cancer

IF 10.7 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
MedComm Pub Date : 2025-10-03 DOI:10.1002/mco2.70391
Zhaoyun Liu, Jiao Lai, Ziyu Ma, Jianhua Pan, Chun Yang, Rong Fu
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引用次数: 0

Abstract

Ubiquitin is a highly conserved small molecule that exists in large quantities in eukaryotic cells and plays a crucial role in protein quality control by phagocytosis and degradation of ubiquitin-modified proteins. The abnormal expression of the ubiquitin–proteasome system (UPS) in cancer leads to the abnormal expression of ubiquitin ligases and ubiquitin-binding enzymes, resulting in the abnormal accumulation of ubiquitinated proteins. Consequently, UPS dysregulation can contribute to tumor initiation, progression, and resistance to therapy. While proteasome inhibitors have shown clinical success, comprehensive reviews integrating upstream UPS components and their therapeutic potential are lacking. This paper reviews the composition of the UPS, its tumor-promoting mechanisms, as well as the small molecule inhibitors and proteasome inhibitors based on this system, including their mechanisms of action and adverse effects, and explores their clinical advances in the treatment of cancer. This review provides a valuable framework for developing next-generation anti-cancer therapies and establishes the UPS as a critical therapeutic target for precision oncology.

Abstract Image

靶向泛素-蛋白酶体系统治疗癌症
泛素是一种高度保守的小分子,大量存在于真核细胞中,通过吞噬和降解泛素修饰的蛋白质,在蛋白质质量控制中起着至关重要的作用。肿瘤中泛素-蛋白酶体系统(ubiquitin- proteasome system, UPS)的异常表达导致泛素连接酶和泛素结合酶的异常表达,导致泛素化蛋白的异常积累。因此,UPS失调可能导致肿瘤的发生、发展和对治疗的抵抗。虽然蛋白酶体抑制剂已显示出临床成功,但整合上游UPS组件及其治疗潜力的综合综述尚缺乏。本文综述了UPS的组成、促肿瘤机制,以及基于该系统的小分子抑制剂和蛋白酶体抑制剂的作用机制和不良反应,并探讨了其在肿瘤治疗中的临床进展。这一综述为开发下一代抗癌疗法提供了一个有价值的框架,并确立了UPS作为精确肿瘤学的关键治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.70
自引率
0.00%
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审稿时长
10 weeks
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