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泛素-蛋白酶体系统参与肿瘤微环境的调控及进展。

Involvement of the ubiquitin-proteasome system in the regulation of the tumor microenvironment and progression.

作者信息

Huang Yulan, Gao Yuan, Lin Zhenghong, Miao Hongming

机构信息

Department of Pathophysiology, College of High Altitude Military Medicine, Army Medical University, Chongqing 400038, China.

School of Life Sciences, Chongqing University, Chongqing 401331, China.

出版信息

Genes Dis. 2024 Feb 2;12(2):101240. doi: 10.1016/j.gendis.2024.101240. eCollection 2025 Mar.


DOI:10.1016/j.gendis.2024.101240
PMID:39759114
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11697063/
Abstract

The tumor microenvironment is a complex environment comprising tumor cells, non-tumor cells, and other critical non-cellular components. Some studies about tumor microenvironment have recently achieved remarkable progress in tumor treatment. As a substantial part of post-translational protein modification, ubiquitination is a crucial player in maintaining protein stability in cell signaling, cell growth, and a series of cellular life activities, which are also essential for regulating tumor cells or other non-tumor cells in the tumor microenvironment. This review focuses on the role and function of ubiquitination and deubiquitination modification in the tumor microenvironment while discussing the prospect of developing inhibitors targeting ubiquity-related enzymes, thereby providing ideas for future research in cancer therapy.

摘要

肿瘤微环境是一个复杂的环境,由肿瘤细胞、非肿瘤细胞和其他关键的非细胞成分组成。最近,一些关于肿瘤微环境的研究在肿瘤治疗方面取得了显著进展。作为蛋白质翻译后修饰的重要组成部分,泛素化在维持细胞信号传导、细胞生长和一系列细胞生命活动中的蛋白质稳定性方面起着关键作用,而这些对于调节肿瘤微环境中的肿瘤细胞或其他非肿瘤细胞也至关重要。本综述重点讨论泛素化和去泛素化修饰在肿瘤微环境中的作用和功能,同时探讨开发靶向泛素相关酶抑制剂的前景,从而为未来癌症治疗研究提供思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d9/11697063/52ac379fc18f/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d9/11697063/9d2501921535/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d9/11697063/32191c2e6170/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d9/11697063/7aa6ff693637/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d9/11697063/cfa902dbb92c/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d9/11697063/52ac379fc18f/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d9/11697063/9d2501921535/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d9/11697063/32191c2e6170/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d9/11697063/7aa6ff693637/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d9/11697063/cfa902dbb92c/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d9/11697063/52ac379fc18f/gr5.jpg

相似文献

[1]
Involvement of the ubiquitin-proteasome system in the regulation of the tumor microenvironment and progression.

Genes Dis. 2024-2-2

[2]
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[3]
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[8]
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[10]
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引用本文的文献

[1]
LZTR1 is a melanoma oncogene that promotes invasion and suppresses apoptosis.

Oncogene. 2025-8-30

[2]
Proteomic Analysis of Protein Ubiquitination Events in Dairy Goats with Fatty Liver.

Animals (Basel). 2025-7-8

[3]
Bibliometric and visualized analysis of global distribution and research frontiers in tumor immune escape.

Front Immunol. 2025-6-5

[4]
Lycobetaine Has Therapeutic Efficacy in Lung Squamous Cell Carcinoma by Targeting USP32 to Trigger Ferroptosis.

Curr Issues Mol Biol. 2025-2-27

本文引用的文献

[1]
Targeting leucine-rich repeat serine/threonine-protein kinase 2 sensitizes pancreatic ductal adenocarcinoma to anti-PD-L1 immunotherapy.

Mol Ther. 2023-10-4

[2]
MDM2 Antagonist Nutlin-3 Stimulates Global DNA Hydroxymethylation by Enhancing p53-TET1 Signaling Axis.

ACS Chem Biol. 2023-10-20

[3]
Coupled deglycosylation-ubiquitination cascade in regulating PD-1 degradation by MDM2.

Cell Rep. 2023-7-25

[4]
TRIM28 promotes the escape of gastric cancer cells from immune surveillance by increasing PD-L1 abundance.

Signal Transduct Target Ther. 2023-6-26

[5]
circ-0000512 inhibits PD-L1 ubiquitination through sponging miR-622/CMTM6 axis to promote triple-negative breast cancer and immune escape.

J Immunother Cancer. 2023-6

[6]
The MDM2-p53 Antagonist Brigimadlin (BI 907828) in Patients with Advanced or Metastatic Solid Tumors: Results of a Phase Ia, First-in-Human, Dose-Escalation Study.

Cancer Discov. 2023-8-4

[7]
MDM2-PROTAC versus MDM2 Inhibitors: Beyond p53 Reactivation.

Cancer Discov. 2023-5-4

[8]
Disruption in networking of KCMF1 linked ubiquitin ligase impairs autophagy in CD8 memory T cells of patients with renal cell carcinoma.

Cancer Lett. 2023-6-28

[9]
Immune checkpoint therapy-current perspectives and future directions.

Cell. 2023-4-13

[10]
Lung adenocarcinoma cell-derived exosomes promote M2 macrophage polarization through transmission of miR-3153 to activate the JNK signaling pathway.

Hum Mol Genet. 2023-6-19

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