USP43 在肿瘤发生中的作用机制:文献综述

Ziqi Zhao, Meichen Liu, Zhikun Lin, Mengru Zhu, Linlin Lv, Xinqing Zhu, Rui Fan, Abdullah Al-danakh, Hui He, Guang Tan
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引用次数: 0

摘要

蛋白质的泛素化对控制蛋白质降解和调节基本细胞过程至关重要。去泛素酶(DUBs)能够清除目标底物上的泛素并调节信号传导,因此已成为与癌症和其他疾病相关的多种途径的重要调节因子。因此,它们是癌症和其他危及生命疾病的潜在治疗靶点。USP43 属于 DUBs 家族,参与了癌症的发生和发展。本综述旨在全面概述 USP43 与癌症发展有关的现有科学证据。此外,它还将研究以 DUBs 为靶点的潜在小分子抑制剂,这些抑制剂可能具有抗癌药物的功能。
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The mechanism of USP43 in the development of tumor: a literature review
Ubiquitination of the proteins is crucial for governing protein degradation and regulating fundamental cellular processes. Deubiquitinases (DUBs) have emerged as significant regulators of multiple pathways associated with cancer and other diseases, owing to their capacity to remove ubiquitin from target substrates and modulate signaling. Consequently, they represent potential therapeutic targets for cancer and other life-threatening conditions. USP43 belongs to the DUBs family involved in cancer development and progression. This review aims to provide a comprehensive overview of the existing scientific evidence implicating USP43 in cancer development. Additionally, it will investigate potential small-molecule inhibitors that target DUBs that may have the capability to function as anti-cancer medicines.
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