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本文引用的文献

1
Battling colorectal cancer via s-triazine-based MMP-10/13 inhibitors armed with electrophilic warheads for concomitant ferroptosis induction; the first-in-class dual-acting agents.通过基于三嗪的 MMP-10/13 抑制剂与亲电弹头联合作用诱导同时发生的铁死亡来对抗结直肠癌;一类首创的双重作用药物。
Bioorg Chem. 2023 Dec;141:106839. doi: 10.1016/j.bioorg.2023.106839. Epub 2023 Sep 7.
2
In vitro CRISPR screening uncovers CRTC3 as a regulator of IFN-γ-induced ferroptosis of hepatocellular carcinoma.体外CRISPR筛选揭示CRTC3是IFN-γ诱导的肝细胞癌铁死亡的调节因子。
Cell Death Discov. 2023 Sep 4;9(1):331. doi: 10.1038/s41420-023-01630-8.
3
Metabolism, metabolites, and macrophages in cancer.癌症中的代谢、代谢物和巨噬细胞。
J Hematol Oncol. 2023 Jul 25;16(1):80. doi: 10.1186/s13045-023-01478-6.
4
Understanding sorafenib-induced ferroptosis and resistance mechanisms: Implications for cancer therapy.了解索拉非尼诱导的铁死亡及其耐药机制:对癌症治疗的启示。
Eur J Pharmacol. 2023 Sep 15;955:175913. doi: 10.1016/j.ejphar.2023.175913. Epub 2023 Jul 17.
5
Ferroptosis of immune cells in the tumor microenvironment.肿瘤微环境中免疫细胞的铁死亡。
Trends Pharmacol Sci. 2023 Aug;44(8):542-552. doi: 10.1016/j.tips.2023.06.005. Epub 2023 Jun 27.
6
Ferroptosis-mediated immune responses in cancer.铁死亡介导的癌症免疫反应。
Front Immunol. 2023 May 30;14:1188365. doi: 10.3389/fimmu.2023.1188365. eCollection 2023.
7
Tumor microenvironment signaling and therapeutics in cancer progression.肿瘤微环境信号与癌症进展中的治疗策略。
Cancer Commun (Lond). 2023 May;43(5):525-561. doi: 10.1002/cac2.12416. Epub 2023 Apr 2.
8
The evolving tumor microenvironment: From cancer initiation to metastatic outgrowth.不断演变的肿瘤微环境:从癌症起始到转移灶生长
Cancer Cell. 2023 Mar 13;41(3):374-403. doi: 10.1016/j.ccell.2023.02.016.
9
STAT proteins in cancer: orchestration of metabolism.癌症中的 STAT 蛋白:代谢的协调。
Nat Rev Cancer. 2023 Mar;23(3):115-134. doi: 10.1038/s41568-022-00537-3. Epub 2023 Jan 3.
10
The role of IL-6/JAK2/STAT3 signaling pathway in cancers.白细胞介素-6/Janus激酶2/信号转导和转录激活因子3信号通路在癌症中的作用
Front Oncol. 2022 Dec 16;12:1023177. doi: 10.3389/fonc.2022.1023177. eCollection 2022.

促炎细胞因子、铁死亡与癌症

Pro-inflammatory Cytokines, Ferroptosis, and Cancer.

作者信息

Vartanian A A, Kosorukov V S

机构信息

N.N. Blokhin National Medical Research Center of Oncology of the Ministry of Health of Russia, Moscow, 115478 Russian Federation.

出版信息

Acta Naturae. 2025 Jan-Mar;17(1):4-10. doi: 10.32607/actanaturae.27547.

DOI:10.32607/actanaturae.27547
PMID:40264585
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12011187/
Abstract

Ferroptosis, iron-dependent regulated cell death, is induced by the polyunsaturated fatty acid peroxidation of membrane phospholipids and is controlled by glutathione peroxidase 4. In recent years, convincing evidence has emerged, demonstrating a close relationship between chemo-, radio-, immuno-, and targeted therapy resistance and ferroptosis resistance. In this review, we discuss the basic principles of ferroptosis in cancer. Considerable attention is paid to the formation of an immunosuppressive tumor microenvironment. The main focus is centered on the involvement of the excessive, chronic production of pro-inflammatory cytokines in ferroptosis resistance development in tumors.

摘要

铁死亡是一种铁依赖性的程序性细胞死亡,由膜磷脂的多不饱和脂肪酸过氧化诱导,并受谷胱甘肽过氧化物酶4调控。近年来,越来越多的确凿证据表明,化疗、放疗、免疫治疗和靶向治疗耐药性与铁死亡抗性之间存在密切关系。在这篇综述中,我们讨论了癌症中铁死亡的基本原理。我们对免疫抑制性肿瘤微环境的形成给予了相当多的关注。主要关注点集中在促炎细胞因子的过度、慢性产生在肿瘤铁死亡抗性发展中的作用。