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USP43在肿瘤发生发展中的作用机制:文献综述

The mechanism of USP43 in the development of tumor: a literature review.

作者信息

Zhao Ziqi, Liu Meichen, Lin Zhikun, Zhu Mengru, Lv Linlin, Zhu Xinqing, Fan Rui, Al-Danakh Abdullah, He Hui, Tan Guang

机构信息

Department of General Surgery, The First Affiliated Hospital of Dalian Medical University, Dalian Medical University, Dalian 116011, China.

Department of Neurology, The First Affiliated Hospital of Dalian Medical University, Dalian Medical University, Dalian 116011, China.

出版信息

Aging (Albany NY). 2024 Apr 8;16(7):6613-6626. doi: 10.18632/aging.205731.

DOI:10.18632/aging.205731
PMID:38613804
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11042928/
Abstract

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.

摘要

蛋白质的泛素化对于控制蛋白质降解和调节基本细胞过程至关重要。去泛素化酶(DUBs)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,这是因为它们能够从靶底物上去除泛素并调节信号传导。因此,它们是癌症和其他危及生命疾病的潜在治疗靶点。USP43属于参与癌症发生和发展的去泛素化酶家族。本综述旨在全面概述现有科学证据,表明USP43与癌症发生有关。此外,还将研究靶向去泛素化酶的潜在小分子抑制剂,这些抑制剂可能具有作为抗癌药物的功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2276/11042928/2231f10ba260/aging-16-205731-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2276/11042928/428593b4f26b/aging-16-205731-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2276/11042928/2231f10ba260/aging-16-205731-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2276/11042928/428593b4f26b/aging-16-205731-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2276/11042928/2231f10ba260/aging-16-205731-g002.jpg

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Cell Death Dis. 2024 Jan 13;15(1):44. doi: 10.1038/s41419-024-06446-7.
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USP43 impairs cisplatin sensitivity in epithelial ovarian cancer through HDAC2-dependent regulation of Wnt/β-catenin signaling pathway.USP43 通过依赖于 HDAC2 的调控 Wnt/β-catenin 信号通路来损害上皮性卵巢癌对顺铂的敏感性。
Apoptosis. 2024 Feb;29(1-2):210-228. doi: 10.1007/s10495-023-01873-x. Epub 2023 Dec 12.
3
Ubiquitin-Specific Protease 43 Impacts Pancreatic Ductal Adenocarcinoma Prognosis by Altering Its Proliferation and Infiltration of Surrounding Immune Cells.
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J Immunol Res. 2023 Apr 2;2023:4311388. doi: 10.1155/2023/4311388. eCollection 2023.
4
Ca2.2-NFAT2-USP43 axis promotes invadopodia formation and breast cancer metastasis through cortactin stabilization.钙离子-NFAT2-USP43 轴通过稳定 cortactin 促进侵袭伪足形成和乳腺癌转移。
Cell Death Dis. 2022 Sep 22;13(9):812. doi: 10.1038/s41419-022-05174-0.
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A Six-Gene Prognostic and Predictive Radiotherapy-Based Signature for Early and Locally Advanced Stages in Non-Small-Cell Lung Cancer.一种基于放疗的六基因预后和预测标志物,用于非小细胞肺癌早期和局部晚期阶段
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