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肺癌中的铁死亡:双重作用、多层次调控及新治疗策略

Ferroptosis in lung cancer: dual role, multi-level regulation, and new therapeutic strategies.

作者信息

Li Yunbin, Li Xiaosong, Li Jian

机构信息

Department of Thoracic Surgery, The Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China.

出版信息

Front Oncol. 2024 Mar 7;14:1360638. doi: 10.3389/fonc.2024.1360638. eCollection 2024.

DOI:10.3389/fonc.2024.1360638
PMID:38515565
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10955378/
Abstract

Lung cancer is a highly prevalent malignant tumor worldwide, with high incidence and death rates. Recently, there has been increasing recognition of the role of ferroptosis, a unique cell death mechanism, in lung cancer. This review aims to summarize the current research progress on the relationship between ferroptosis and lung cancer. It also provides a comprehensive analysis of the regulatory processes of ferroptosis in various stages, including epigenetics, transcription, post-transcription, translation, and post-translation. Additionally, the review explores the dual nature of ferroptosis in lung cancer progression, which presents interesting therapeutic possibilities. On one hand, ferroptosis can promote the escape of immune surveillance and reduce the efficacy of treatment in the early stages of tumors. On the other hand, it can counter drug resistance, enhance radiosensitivity, and promote immunotherapy. The article also discusses various combination treatment strategies based on the mechanism of ferroptosis. Overall, this review offers a holistic perspective on the role of ferroptosis in the onset, progression, and treatment of lung cancer. It aims to contribute to future research and clinical interventions in this field.

摘要

肺癌是全球高度流行的恶性肿瘤,发病率和死亡率都很高。最近,一种独特的细胞死亡机制——铁死亡在肺癌中的作用得到了越来越多的认识。这篇综述旨在总结铁死亡与肺癌关系的当前研究进展。它还全面分析了铁死亡在各个阶段的调控过程,包括表观遗传学、转录、转录后、翻译和翻译后阶段。此外,该综述探讨了铁死亡在肺癌进展中的双重性质,这呈现出有趣的治疗可能性。一方面,铁死亡可促进免疫逃逸并降低肿瘤早期的治疗效果。另一方面,它可以对抗耐药性、增强放射敏感性并促进免疫治疗。本文还讨论了基于铁死亡机制的各种联合治疗策略。总体而言,这篇综述对铁死亡在肺癌发生、发展和治疗中的作用提供了全面的视角。它旨在为该领域的未来研究和临床干预做出贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f11/10955378/cce5ca107d1f/fonc-14-1360638-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f11/10955378/96aa0d308af7/fonc-14-1360638-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f11/10955378/cce5ca107d1f/fonc-14-1360638-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f11/10955378/96aa0d308af7/fonc-14-1360638-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f11/10955378/cce5ca107d1f/fonc-14-1360638-g002.jpg

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引用本文的文献

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MedComm (2020). 2025 Feb 23;6(3):e70116. doi: 10.1002/mco2.70116. eCollection 2025 Mar.
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Broadening horizons: research on ferroptosis in lung cancer and its potential therapeutic targets.拓宽视野:肺癌中铁死亡的研究及其潜在治疗靶点
Front Immunol. 2025 Jan 23;16:1542844. doi: 10.3389/fimmu.2025.1542844. eCollection 2025.
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Ferroptosis: emerging roles in lung cancer and potential implications in biological compounds.

本文引用的文献

1
Phospholipids with two polyunsaturated fatty acyl tails promote ferroptosis.带有两条多不饱和脂肪酰基尾巴的磷脂会促进铁死亡。
Cell. 2024 Feb 29;187(5):1177-1190.e18. doi: 10.1016/j.cell.2024.01.030. Epub 2024 Feb 15.
2
Identification of hyperoxidized PRDX3 as a ferroptosis marker reveals ferroptotic damage in chronic liver diseases.鉴定过氧化物还原酶 3 (PRDX3)的过氧化物化为铁死亡标志物,揭示了慢性肝脏疾病中的铁死亡损伤。
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The crosstalk between ferroptosis and anti-tumor immunity in the tumor microenvironment: molecular mechanisms and therapeutic controversy.
铁死亡:在肺癌中的新作用及对生物化合物的潜在影响
Front Pharmacol. 2024 May 9;15:1374182. doi: 10.3389/fphar.2024.1374182. eCollection 2024.
肿瘤微环境中铁死亡与抗肿瘤免疫的相互作用:分子机制与治疗争议
Cancer Commun (Lond). 2023 Oct;43(10):1071-1096. doi: 10.1002/cac2.12487. Epub 2023 Sep 17.
4
ROS induced lipid peroxidation and their role in ferroptosis.活性氧诱导的脂质过氧化及其在铁死亡中的作用。
Front Cell Dev Biol. 2023 Aug 1;11:1226044. doi: 10.3389/fcell.2023.1226044. eCollection 2023.
5
A novel quinoline derivative, DFIQ, sensitizes NSCLC cells to ferroptosis by promoting oxidative stress accompanied by autophagic dysfunction and mitochondrial damage.一种新型喹啉衍生物DFIQ通过促进氧化应激,伴随自噬功能障碍和线粒体损伤,使非小细胞肺癌细胞对铁死亡敏感。
Cancer Cell Int. 2023 Aug 16;23(1):171. doi: 10.1186/s12935-023-02984-w.
6
EGCG alleviates obesity-exacerbated lung cancer progression by STAT1/SLC7A11 pathway and gut microbiota.表没食子儿茶素没食子酸酯通过STAT1/SLC7A11通路和肠道微生物群减轻肥胖加剧的肺癌进展。
J Nutr Biochem. 2023 Oct;120:109416. doi: 10.1016/j.jnutbio.2023.109416. Epub 2023 Jul 13.
7
oxidative polymerization of platinum(iv) prodrugs in pore-confined spaces of CaCO nanoparticles for cancer chemoimmunotherapy.用于癌症化学免疫治疗的铂(IV)前药在碳酸钙纳米颗粒孔限空间内的氧化聚合
Chem Sci. 2023 Jun 2;14(25):7005-7015. doi: 10.1039/d3sc02264a. eCollection 2023 Jun 28.
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Ferroptosis-related gene HIC1 in the prediction of the prognosis and immunotherapeutic efficacy with immunological activity.铁死亡相关基因 HIC1 与免疫活性预测预后和免疫治疗疗效的关系。
Front Immunol. 2023 Jun 14;14:1182030. doi: 10.3389/fimmu.2023.1182030. eCollection 2023.
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Butyrate enhances erastin-induced ferroptosis of lung cancer cells via modulating the ATF3/SLC7A11 pathway.丁酸盐通过调节 ATF3/SLC7A11 通路增强依维莫司诱导的肺癌细胞铁死亡。
Environ Toxicol. 2024 Feb;39(2):529-538. doi: 10.1002/tox.23857. Epub 2023 Jun 21.
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Isoorientin reverses lung cancer drug resistance by promoting ferroptosis via the SIRT6/Nrf2/GPX4 signaling pathway.异土木香内酯通过 SIRT6/Nrf2/GPX4 信号通路促进铁死亡逆转肺癌耐药。
Eur J Pharmacol. 2023 Sep 5;954:175853. doi: 10.1016/j.ejphar.2023.175853. Epub 2023 Jun 16.