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铁死亡与肿瘤免疫。

Ferroptosis and tumor immunity.

作者信息

Tao Qian, Liu Nian, Chen Jing, Wu Jie, Li Jie, Chen Xiang, Peng Cong

机构信息

Department of Dermatology, Xiangya Hospital, Central South University, Changsha 410008.

Hunan Key Laboratory of Skin Cancer and Psoriasis, Changsha 410008.

出版信息

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2024 Aug 28;49(8):1309-1315. doi: 10.11817/j.issn.1672-7347.2024.240389.

DOI:10.11817/j.issn.1672-7347.2024.240389
PMID:39788519
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11628223/
Abstract

Ferroptosis is a unique form of cell death driven by iron-dependent lipid peroxidation, with regulatory mechanisms involving metabolic dysregulation and imbalance in redox systems. Ferroptosis is closely related to various immune cells in the tumor immune microenvironment, including both anti-tumor and pro-tumor immune cells, and it demonstrates significant potential in tumor immunotherapy. A systematic review of the regulatory mechanisms of ferroptosis and its relationship with immune cells can provide deeper insights into its application prospects in tumor immunotherapy.

摘要

铁死亡是一种由铁依赖性脂质过氧化驱动的独特细胞死亡形式,其调节机制涉及代谢失调和氧化还原系统失衡。铁死亡与肿瘤免疫微环境中的各种免疫细胞密切相关,包括抗肿瘤和促肿瘤免疫细胞,并且在肿瘤免疫治疗中显示出巨大潜力。对铁死亡的调节机制及其与免疫细胞的关系进行系统综述,可以更深入地了解其在肿瘤免疫治疗中的应用前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63bf/11628223/2c5b4356a0cb/ZhongNanDaXueXueBaoYiXueBan-49-8-1309-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63bf/11628223/aaef7058f4c9/ZhongNanDaXueXueBaoYiXueBan-49-8-1309-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63bf/11628223/2c5b4356a0cb/ZhongNanDaXueXueBaoYiXueBan-49-8-1309-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63bf/11628223/aaef7058f4c9/ZhongNanDaXueXueBaoYiXueBan-49-8-1309-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63bf/11628223/2c5b4356a0cb/ZhongNanDaXueXueBaoYiXueBan-49-8-1309-g002.jpg

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本文引用的文献

1
DEPDC5 protects CD8 T cells from ferroptosis by limiting mTORC1-mediated purine catabolism.DEPDC5通过限制mTORC1介导的嘌呤分解代谢来保护CD8 T细胞免受铁死亡。
Cell Discov. 2024 May 20;10(1):53. doi: 10.1038/s41421-024-00682-z.
2
Dendritic Polylysine with Paclitaxel and Triptolide Codelivery for Enhanced Cancer Ferroptosis through the Accumulation of ROS.负载紫杉醇和雷公藤甲素的树枝状聚赖氨酸共递送通过活性氧的积累增强癌症铁死亡
ACS Appl Mater Interfaces. 2024 Apr 10. doi: 10.1021/acsami.4c00558.
3
Mefloquine enhances the efficacy of anti-PD-1 immunotherapy via IFN-γ-STAT1-IRF1-LPCAT3-induced ferroptosis in tumors.
甲氟喹通过IFN-γ-STAT1-IRF1-LPCAT3诱导的肿瘤铁死亡增强抗PD-1免疫疗法的疗效。
J Immunother Cancer. 2024 Mar 11;12(3):e008554. doi: 10.1136/jitc-2023-008554.
4
The crosstalk between ferroptosis and anti-tumor immunity in the tumor microenvironment: molecular mechanisms and therapeutic controversy.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.
5
Intermittent dietary methionine deprivation facilitates tumoral ferroptosis and synergizes with checkpoint blockade.间歇性膳食蛋氨酸剥夺促进肿瘤细胞铁死亡,并与检查点阻断协同作用。
Nat Commun. 2023 Aug 8;14(1):4758. doi: 10.1038/s41467-023-40518-0.
6
Therapeutic strategies for EGFR-mutated non-small cell lung cancer patients with osimertinib resistance.奥希替尼耐药的表皮生长因子受体突变型非小细胞肺癌患者的治疗策略。
J Hematol Oncol. 2022 Dec 8;15(1):173. doi: 10.1186/s13045-022-01391-4.
7
Autophagy, ferroptosis, pyroptosis, and necroptosis in tumor immunotherapy.肿瘤免疫治疗中的自噬、铁死亡、细胞焦亡和坏死性凋亡。
Signal Transduct Target Ther. 2022 Jun 20;7(1):196. doi: 10.1038/s41392-022-01046-3.
8
Dual Effect of Immune Cells within Tumour Microenvironment: Pro- and Anti-Tumour Effects and Their Triggers.肿瘤微环境中免疫细胞的双重作用:促肿瘤和抗肿瘤作用及其触发因素。
Cancers (Basel). 2022 Mar 25;14(7):1681. doi: 10.3390/cancers14071681.
9
CD8 T cells and fatty acids orchestrate tumor ferroptosis and immunity via ACSL4.CD8 T 细胞和脂肪酸通过 ACSL4 调控肿瘤铁死亡和免疫。
Cancer Cell. 2022 Apr 11;40(4):365-378.e6. doi: 10.1016/j.ccell.2022.02.003. Epub 2022 Feb 24.
10
Immunogenic cell stress and death.免疫原性细胞应激和死亡。
Nat Immunol. 2022 Apr;23(4):487-500. doi: 10.1038/s41590-022-01132-2. Epub 2022 Feb 10.