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实体瘤治疗耐药机制中的线粒体自噬

Mitophagy in the mechanisms of treatment resistance in solid tumors.

作者信息

Yan Xiaoyi, Ding Hui, Ren Mengxiao, Zang Lei

机构信息

The Third Department of Geriatrics, Weifang People's Hospital, Weifang, Shandong, China.

出版信息

Oncol Rev. 2025 Jul 21;19:1607983. doi: 10.3389/or.2025.1607983. eCollection 2025.

DOI:10.3389/or.2025.1607983
PMID:40761374
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12318953/
Abstract

This review aims to explore the mechanisms by which mitophagy contributes to treatment resistance in solid tumors. As advancements in cancer therapies continue to evolve, treatment resistance emerges as a significant barrier to successful tumor management. Mitophagy, a specific form of cellular autophagy, has been implicated in the survival, proliferation, and drug resistance of tumor cells. This article will summarize the latest research findings and analyze how mitophagy impacts the biological characteristics of solid tumors, thereby revealing its potential implications in cancer treatment strategies. By understanding the role of mitophagy in the context of treatment resistance, we may uncover new therapeutic targets and strategies to enhance the efficacy of existing cancer treatments.

摘要

本综述旨在探讨线粒体自噬导致实体瘤治疗耐药的机制。随着癌症治疗的不断进步,治疗耐药已成为成功管理肿瘤的重大障碍。线粒体自噬作为细胞自噬的一种特殊形式,与肿瘤细胞的存活、增殖和耐药性有关。本文将总结最新研究成果,并分析线粒体自噬如何影响实体瘤的生物学特性,从而揭示其在癌症治疗策略中的潜在意义。通过了解线粒体自噬在治疗耐药背景下的作用,我们可能会发现新的治疗靶点和策略,以提高现有癌症治疗的疗效。

相似文献

1
Mitophagy in the mechanisms of treatment resistance in solid tumors.实体瘤治疗耐药机制中的线粒体自噬
Oncol Rev. 2025 Jul 21;19:1607983. doi: 10.3389/or.2025.1607983. eCollection 2025.
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本文引用的文献

1
A glutathione-responsive ferroptotic inducer with elevated labile iron pool and self-supplied peroxide for chemodynamic therapy.一种具有升高的不稳定铁池和自供应过氧化物的谷胱甘肽响应性铁死亡诱导剂,用于化学动力学疗法。
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Engineering charge density in s-block potassium single-atom nanozyme for amplified ferroptosis in glioblastoma therapy.用于胶质母细胞瘤治疗中增强铁死亡的s区钾单原子纳米酶的工程电荷密度
Mater Today Bio. 2025 May 21;32:101889. doi: 10.1016/j.mtbio.2025.101889. eCollection 2025 Jun.
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USP14 inhibits mitophagy and promotes tumorigenesis and chemosensitivity through deubiquitinating BAG4 in microsatellite instability-high colorectal cancer.
在微卫星高度不稳定的结直肠癌中,USP14通过去泛素化BAG4抑制线粒体自噬,促进肿瘤发生和化疗敏感性。
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Ruthenium Single-Atom Nanozyme Driven Sonosensitizer with Oxygen Vacancies Enhances Electron-Hole Separation Efficacy and Remodels Tumor Microenvironment for Sonodynamic-Amplified Ferroptosis.具有氧空位的钌单原子纳米酶驱动的声敏剂增强电子-空穴分离效率并重塑肿瘤微环境以实现声动力放大的铁死亡
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Tubeimoside I induces mitophagy by activating the PINK1/Parkin/Mfn2 signaling pathway in acute myeloid leukemia cells.土贝母苷甲通过激活急性髓系白血病细胞中的PINK1/Parkin/Mfn2信号通路诱导线粒体自噬。
Transl Oncol. 2025 May;55:102355. doi: 10.1016/j.tranon.2025.102355. Epub 2025 Mar 19.
6
Calnexin promotes glioblastoma progression by inducing protective mitophagy through the MEK/ERK/BNIP3 pathway.钙连蛋白通过MEK/ERK/BNIP3途径诱导保护性线粒体自噬,从而促进胶质母细胞瘤进展。
Theranostics. 2025 Jan 27;15(6):2624-2648. doi: 10.7150/thno.105591. eCollection 2025.
7
Targeting ceramide transfer protein sensitizes AML to FLT3 inhibitors via a GRP78-ATF6-CHOP axis.靶向神经酰胺转移蛋白通过GRP78-ATF6-CHOP轴使急性髓系白血病对FLT3抑制剂敏感。
Nat Commun. 2025 Feb 4;16(1):1358. doi: 10.1038/s41467-025-56520-7.
8
Improved Efficacy of Triple-Negative Breast Cancer Immunotherapy via Hydrogel-Based Co-Delivery of CAR-T Cells and Mitophagy Agonist.通过基于水凝胶的CAR-T细胞和线粒体自噬激动剂共递送提高三阴性乳腺癌免疫治疗的疗效
Adv Sci (Weinh). 2025 Apr;12(14):e2409835. doi: 10.1002/advs.202409835. Epub 2025 Jan 22.
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Triphenylphosphine-modified cyclometalated iridium complexes as mitochondria-targeting anticancer agents with enhanced selectivity.三苯基膦修饰的环金属化铱配合物作为具有增强选择性的线粒体靶向抗癌剂。
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Hypoxia-selective prodrug restrains tumor cells through triggering mitophagy and inducing apoptosis.缺氧选择性前药通过触发线粒体自噬和诱导凋亡来抑制肿瘤细胞。
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