USP1去泛素酶在癌症发病和治疗中的作用。

IF 1.4 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Acta biochimica Polonica Pub Date : 2023-06-12 DOI:10.18388/abp.2020_6636
Svitlana Antonenko, Michael Zavelevich, Gennady Telegeev
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引用次数: 0

摘要

泛素特异性蛋白酶1 (USP1)是一种重要的去泛素化酶(DUB),参与维持基因组完整性、细胞周期和细胞稳态。USP1过表达是多种癌症的特征,与不良预后相关。这篇综述总结了最近在理解去泛素酶USP1在肿瘤蛋白和肿瘤抑制因子稳定中的作用方面的知识,作为癌症发生和进展的关键事件。讨论了USP1参与一些常见人类癌症的可能机制。大量数据表明,抑制USP1抑制恶性肿瘤细胞的增殖和生存能力,使其对放射敏感,增加其对各种化疗药物的敏感性,这为恶性肿瘤的联合治疗开辟了新的机会。
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The role of USP1 deubiquitinase in the pathogenesis and therapy of cancer.

Ubiquitin-specific protease 1 (USP1) is an important deubiquitinating enzyme (DUB) involved in the maintenance of genome integrity, cell cycle, and cell homeostasis. USP1 overexpression is a characteristic feature of various cancers, correlating with a poor prognosis. The review summarizes the recent knowledge in understanding the role of deubiquitinase USP1 in the stabilization of oncoproteins and tumor suppressors, as a critical event in cancer development and progression. The putative mechanisms of USP1 involvement in some prevalent human cancers are discussed. The numerous data demonstrate that inhibition of USP1 suppresses the proliferation and viability of malignant cells, sensitizes them to radiation and increases their sensitivity to various chemo- therapeutic agents, which opens up new opportunities for combined therapy of malignant neoplasms.

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来源期刊
Acta biochimica Polonica
Acta biochimica Polonica 生物-生化与分子生物学
CiteScore
2.40
自引率
0.00%
发文量
99
审稿时长
4-8 weeks
期刊介绍: Acta Biochimica Polonica is a journal covering enzymology and metabolism, membranes and bioenergetics, gene structure and expression, protein, nucleic acid and carbohydrate structure and metabolism.
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