The ubiquitin-proteasome system in the regulation of tumor dormancy and recurrence.

Bashar A Alhasan, Alexey V Morozov, Irina V Guzhova, Boris A Margulis
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Abstract

Tumor recurrence is a mechanism triggered in sparse populations of cancer cells that usually remain in a quiescent state after strict stress and/or therapeutic factors, which is affected by a variety of autocrine and microenvironmental cues. Despite thorough investigations, the biology of dormant and/or cancer stem cells is still not fully elucidated, as for the mechanisms of their reawakening, while only the major molecular patterns driving the relapse process have been identified to date. These molecular patterns profoundly interfere with the elements of cellular proteostasis systems that support the efficiency of the recurrence process. As a major proteostasis machinery, we review the role of the ubiquitin-proteasome system (UPS) in tumor cell dormancy and reawakening, devoting particular attention to the functions of its components, E3 ligases, deubiquitinating enzymes and proteasomes in cancer recurrence. We demonstrate how UPS components functionally or mechanistically interact with the pivotal proteins implicated in the recurrence program and reveal that modulators of the UPS hold promise to become an efficient adjuvant therapy for eradicating refractory tumor cells to impede tumor relapse.

泛素-蛋白酶体系统对肿瘤休眠和复发的调控。
肿瘤复发是稀少的癌细胞群触发的一种机制,这些癌细胞在受到严格的压力和/或治疗因素后通常处于静止状态,并受到各种自分泌和微环境线索的影响。尽管进行了深入研究,但休眠和/或癌症干细胞的生物学特性及其苏醒机制仍未完全阐明。这些分子模式严重干扰了支持复发过程效率的细胞蛋白稳态系统要素。作为一种主要的蛋白稳态机制,我们回顾了泛素-蛋白酶体系统(UPS)在肿瘤细胞休眠和苏醒中的作用,并特别关注了其组成成分、E3连接酶、去泛素化酶和蛋白酶体在癌症复发中的功能。我们展示了 UPS 成分如何在功能上或机制上与复发程序中的关键蛋白相互作用,并揭示了 UPS 的调节剂有望成为根除难治性肿瘤细胞的有效辅助疗法,从而阻碍肿瘤复发。
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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