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泛素连接酶和蛋白酶体在肿瘤发生中的作用:抗癌治疗的新靶点。

Role of ubiquitin ligases and the proteasome in oncogenesis: novel targets for anticancer therapies.

机构信息

University of Colorado School of Medicine, Aurora, CO,

出版信息

J Clin Oncol. 2013 Mar 20;31(9):1231-8. doi: 10.1200/JCO.2012.44.0958. Epub 2013 Jan 28.

Abstract

The ubiquitin proteasome system (UPS) regulates the ubiquitination, and thus degradation and turnover, of many proteins vital to cellular regulation and function. The UPS comprises a sequential series of enzymatic processes using four key enzyme families: E1 (ubiquitin-activating enzymes), E2 (ubiquitin-carrier proteins), E3 (ubiquitin-protein ligases), and E4 (ubiquitin chain assembly factors). Because the UPS is a crucial regulator of the cell cycle, and abnormal cell-cycle control can lead to oncogenesis, aberrancies within the UPS pathway can result in a malignant cellular phenotype and thus has become an attractive target for novel anticancer agents. This article will provide an overall review of the mechanics of the UPS, describe aberrancies leading to cancer, and give an overview of current drug therapies selectively targeting the UPS.

摘要

泛素蛋白酶体系统(UPS)调节许多对细胞调节和功能至关重要的蛋白质的泛素化,从而降解和周转。UPS 由一系列连续的酶促过程组成,使用四种关键的酶家族:E1(泛素激活酶)、E2(泛素载体蛋白)、E3(泛素蛋白连接酶)和 E4(泛素链组装因子)。由于 UPS 是细胞周期的关键调节剂,并且异常的细胞周期控制可能导致肿瘤发生,因此 UPS 途径中的异常会导致恶性细胞表型,因此已成为新型抗癌药物的有吸引力的靶标。本文将全面综述 UPS 的机制,描述导致癌症的异常,并概述当前选择性靶向 UPS 的药物治疗方法。

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