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铁死亡:一把双刃剑,增强肿瘤的辐射敏感性并加剧辐射诱导的损伤。

Ferroptosis: a double-edged sword that enhances radiation sensitivity and facilitates radiation-induced injury in tumors.

作者信息

Liu Yang, Zhan Jianhao, Wang Jisheng, Zeng Xiaoping, Liu Shanshan, Huang Le, Niu Liyan, Sun Chengpeng, Ding Zijun, Xing Yan, Zhou Zhengyu, Li Xiaoying, Li Qing, Wang Hongmei

机构信息

Department of Oncology, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, China.

The First School of Clinical Medicine of Nanchang University, Nanchang University, Nanchang, Jiangxi, China.

出版信息

Front Immunol. 2025 Jul 10;16:1591172. doi: 10.3389/fimmu.2025.1591172. eCollection 2025.

DOI:10.3389/fimmu.2025.1591172
PMID:40709182
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12287047/
Abstract

Cell death is a crucial mechanism by which radiotherapy eliminates tumor cells. Ferroptosis, characterized by intracellular iron overload and lipid peroxidation, represents a distinct form of programmed cell death. Recent research has demonstrated that numerous malignant tumors exhibit high sensitivity to ferroptosis. Therefore, the induction of ferroptosis in tumor cells has emerged as a promising approach to overcome apoptosis resistance and increase sensitivity to radiotherapy. In this review, we aim to shed light on ferroptosis and its dual roles in both enhancing radiation sensitivity in tumor cells and facilitating radiation-induced injury. Then we discussed the contradiction of ferroptosis between radiation sensitivity and radiation-induced injury, providing valuable insights and directions for the advancement of clinical tumor radiotherapy.

摘要

细胞死亡是放射治疗消除肿瘤细胞的关键机制。铁死亡以细胞内铁过载和脂质过氧化为特征,是一种独特的程序性细胞死亡形式。最近的研究表明,许多恶性肿瘤对铁死亡表现出高度敏感性。因此,诱导肿瘤细胞发生铁死亡已成为一种有前景的方法,可克服细胞凋亡抗性并提高放疗敏感性。在本综述中,我们旨在阐明铁死亡及其在增强肿瘤细胞放射敏感性和促进辐射诱导损伤方面的双重作用。然后我们讨论了铁死亡在放射敏感性和辐射诱导损伤之间的矛盾,为临床肿瘤放疗的进展提供了有价值的见解和方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf5d/12287047/da542dd6003b/fimmu-16-1591172-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf5d/12287047/314bdcfcaec5/fimmu-16-1591172-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf5d/12287047/7b68b444bc5a/fimmu-16-1591172-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf5d/12287047/e837e9428c4e/fimmu-16-1591172-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf5d/12287047/da542dd6003b/fimmu-16-1591172-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf5d/12287047/314bdcfcaec5/fimmu-16-1591172-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf5d/12287047/7b68b444bc5a/fimmu-16-1591172-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf5d/12287047/e837e9428c4e/fimmu-16-1591172-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf5d/12287047/da542dd6003b/fimmu-16-1591172-g004.jpg

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本文引用的文献

1
Inhibition of Glutathione Pathway by Oleanolic Acid via PSAT1 Leads to Ferroptosis in Colorectal Cancer.齐墩果酸通过PSAT1抑制谷胱甘肽途径导致结直肠癌铁死亡
Drug Dev Res. 2025 May;86(3):e70097. doi: 10.1002/ddr.70097.
2
Galectin-13 reduces membrane localization of SLC7A11 for ferroptosis propagation.半乳糖凝集素-13降低SLC7A11的膜定位以促进铁死亡。
Nat Chem Biol. 2025 Apr 17. doi: 10.1038/s41589-025-01888-2.
3
Radiation-induced ferroptosis via liposomal delivery of 7-Dehydrocholesterol.通过脂质体递送7-脱氢胆固醇诱导辐射性铁死亡
J Nanobiotechnology. 2025 Mar 26;23(1):249. doi: 10.1186/s12951-025-03303-3.
4
Curcumin inhibits ferroptosis-mediated vascular occlusion by regulating the CXCL10/CXCR3 axis in retinopathy of prematurity.姜黄素通过调节早产儿视网膜病变中的CXCL10/CXCR3轴来抑制铁死亡介导的血管闭塞。
Mol Med. 2025 Mar 24;31(1):113. doi: 10.1186/s10020-025-01161-1.
5
Monounsaturated fatty acids promote cancer radioresistance by inhibiting ferroptosis through ACSL3.单不饱和脂肪酸通过ACSL3抑制铁死亡来促进癌症放射抗性。
Cell Death Dis. 2025 Mar 18;16(1):184. doi: 10.1038/s41419-025-07516-0.
6
Ferroptosis: when metabolism meets cell death.铁死亡:当新陈代谢遭遇细胞死亡时
Physiol Rev. 2025 Apr 1;105(2):651-706. doi: 10.1152/physrev.00031.2024. Epub 2024 Dec 11.
7
Iron homeostasis and ferroptosis in human diseases: mechanisms and therapeutic prospects.铁稳态和铁死亡在人类疾病中的作用:机制和治疗前景。
Signal Transduct Target Ther. 2024 Oct 14;9(1):271. doi: 10.1038/s41392-024-01969-z.
8
Curcumin pretreatment attenuates myocardial ischemia/reperfusion injury by inhibiting ferroptosis, autophagy and apoptosis via HES1.姜黄素预处理通过抑制 HES1 介导的铁死亡、自噬和凋亡来减轻心肌缺血/再灌注损伤。
Int J Mol Med. 2024 Dec;54(6). doi: 10.3892/ijmm.2024.5434. Epub 2024 Oct 4.
9
Ferroptosis-inducing nanomedicine and targeted short peptide for synergistic treatment of hepatocellular carcinoma.铁死亡诱导纳米医学和靶向短肽用于协同治疗肝细胞癌。
J Nanobiotechnology. 2024 Sep 3;22(1):533. doi: 10.1186/s12951-024-02808-7.
10
Curcumin Induces Autophagy-mediated Ferroptosis by Targeting the PI3K/AKT/mTOR Signaling Pathway in Gastric Cancer.姜黄素通过靶向胃癌中的 PI3K/AKT/mTOR 信号通路诱导自噬性铁死亡。
Turk J Gastroenterol. 2024 Jul 3;35(8):625-33. doi: 10.5152/tjg.2024.23526.