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靶向铁死亡用于宫颈癌的精准医学

Targeting ferroptosis for precision medicine in cervical cancer.

作者信息

Sun Xin, Chen Zhuoxi, Yang Hui, Yu Jianing, Lin Haiyan, Zhang Leiming

机构信息

School of Traditional Chinese Medicine, Binzhou Medical University, Yantai, 264003, China.

The Second School of Clinical Medicine, Binzhou Medical University, Yantai, 264100, China.

出版信息

Apoptosis. 2025 May 7. doi: 10.1007/s10495-025-02120-1.

DOI:10.1007/s10495-025-02120-1
PMID:40335818
Abstract

Cervical cancer (CC) is a prevalent malignant tumor in the female reproductive system, with rising incidence rates among younger women posing a significant public health challenge. Human papillomavirus (HPV) infection is the primary cause, driving carcinogenesis by promoting abnormal proliferation of tumor cells. Ferroptosis is a form of regulated necrosis that is caused by an iron-dependent accumulation of lipid peroxides with rupture of the plasma membrane. Targeting ferroptosis-related molecules and pathways can selectively induce cervical cancer cell death, while alterations in the expression of ferroptosis-related genes provide promising biomarkers for prognostic assessment. Advances in research on biomarkers and molecular targets are improving predictions of therapeutic outcomes, overcoming drug resistance, and optimizing immunotherapy strategies, thereby opening new avenues for precision medicine. This review focuses on the molecular mechanisms underlying ferroptosis in cervical cancer, discusses its potential applications in early diagnosis and prognosis evaluation, and summarizes the latest advancements in targeted therapy, aiming to provide a novel perspective for the clinical management of cervical cancer.

摘要

宫颈癌(CC)是女性生殖系统中一种常见的恶性肿瘤,年轻女性发病率不断上升,这对公共卫生构成了重大挑战。人乳头瘤病毒(HPV)感染是主要病因,通过促进肿瘤细胞异常增殖驱动癌变。铁死亡是一种程序性坏死形式,由铁依赖性脂质过氧化物积累导致质膜破裂引起。靶向铁死亡相关分子和途径可选择性诱导宫颈癌细胞死亡,而铁死亡相关基因表达的改变为预后评估提供了有前景的生物标志物。生物标志物和分子靶点研究的进展正在改善对治疗结果的预测、克服耐药性并优化免疫治疗策略,从而为精准医学开辟新途径。本综述聚焦宫颈癌中铁死亡的分子机制,讨论其在早期诊断和预后评估中的潜在应用,并总结靶向治疗的最新进展,旨在为宫颈癌的临床管理提供新视角。

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本文引用的文献

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Ferroptosis: CD8T cells' blade to destroy tumor cells or poison for self-destruction.铁死亡:CD8+T细胞用于摧毁肿瘤细胞的利刃或自我毁灭的毒药。
Cell Death Discov. 2025 Apr 1;11(1):128. doi: 10.1038/s41420-025-02415-x.
2
Functions and mechanisms of non-histone post-translational modifications in cancer progression.非组蛋白翻译后修饰在癌症进展中的作用及机制
Cell Death Discov. 2025 Mar 31;11(1):125. doi: 10.1038/s41420-025-02410-2.
3
Boric Acid Suppresses Glioblastoma Cellular Survival by Regulating Ferroptosis via SOX10/GPx4/ACSL4 Signalling and Iron Metabolism.
硼酸通过SOX10/谷胱甘肽过氧化物酶4/长链脂酰辅酶A合成酶4信号通路和铁代谢调节铁死亡,从而抑制胶质母细胞瘤细胞存活。
J Cell Mol Med. 2025 Apr;29(7):e70529. doi: 10.1111/jcmm.70529.
4
HPV E6/E7-Induced Acetylation of a Peptide Encoded by a Long Non-Coding RNA Inhibits Ferroptosis to Promote the Malignancy of Cervical Cancer.人乳头瘤病毒E6/E7诱导的长链非编码RNA编码肽的乙酰化抑制铁死亡以促进宫颈癌的恶性发展。
Adv Sci (Weinh). 2025 Mar;12(10):e2414018. doi: 10.1002/advs.202414018. Epub 2025 Jan 21.
5
Unraveling the Ferroptosis-inducing Potential of Methanol Leaves Extract of Via Downregulation of SLC7A11 and GPX4 mRNA Expression in A549 Lung Cancer Cells.通过下调A549肺癌细胞中SLC7A11和GPX4 mRNA表达揭示[植物名称]甲醇叶提取物的铁死亡诱导潜力
Curr Med Chem. 2025;32(7):1442-1456. doi: 10.2174/0109298673343133241011072425.
6
HPV-ferroptosis related genes as biomarkers to predict the prognosis of cervical cancer.人乳头瘤病毒-铁死亡相关基因作为预测宫颈癌预后的生物标志物
Discov Oncol. 2024 Sep 20;15(1):468. doi: 10.1007/s12672-024-01291-8.
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Artificial intelligence strengthenes cervical cancer screening - present and future.人工智能增强宫颈癌筛查 - 现状与未来。
Cancer Biol Med. 2024 Sep 19;21(10):864-79. doi: 10.20892/j.issn.2095-3941.2024.0198.
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Targeting ferroptosis for improved radiotherapy outcomes in HPV-negative head and neck squamous cell carcinoma.靶向铁死亡以改善人乳头瘤病毒阴性头颈部鳞状细胞癌的放疗效果
Mol Oncol. 2025 Feb;19(2):540-557. doi: 10.1002/1878-0261.13720. Epub 2024 Sep 19.
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Int J Mol Sci. 2024 Jul 29;25(15):8284. doi: 10.3390/ijms25158284.