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揭示肿瘤细胞凋亡和铁死亡转录组景观。

A snapshot into the transcriptomic landscape of apoptosis and ferroptosis in cancer.

机构信息

Molecular Cell Biology Department, Weizmann Institute of Science, Rehovot, Israel.

出版信息

Cell Death Dis. 2024 May 29;15(5):371. doi: 10.1038/s41419-024-06766-8.

DOI:10.1038/s41419-024-06766-8
PMID:38811541
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11137012/
Abstract

Apoptosis and ferroptosis are two regulated cell death (RCD) pathways implicated in different human diseases and considered as promising strategies to eliminate cancer cells. These two pathways are characterized by distinct morphological and biochemical properties, induce cell death through different mechanisms, but share common regulators in different cancer types. Although apoptosis and ferroptosis have been extensively studied over the last few years, their transcriptomic responses have not yet been systematically compared due to remarkable variability in the transcriptomic data. Here we provide a brief snapshot of the transcriptomic landscapes of the apoptosis and ferroptosis responses in cancer, discuss their divergent and convergent properties, and implications to cancer therapy.

摘要

细胞凋亡和铁死亡是两种与人类疾病相关的受调控的细胞死亡 (RCD) 途径,被认为是消除癌细胞的有前途的策略。这两种途径的特征在于形态和生化特性不同,通过不同的机制诱导细胞死亡,但在不同类型的癌症中共享共同的调节剂。尽管凋亡和铁死亡在过去几年中得到了广泛研究,但由于转录组数据的显著变异性,它们的转录组反应尚未得到系统比较。在这里,我们简要概述了癌症中凋亡和铁死亡反应的转录组景观,讨论了它们的发散和收敛特性及其对癌症治疗的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b5c/11137012/cb1e3aee1932/41419_2024_6766_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b5c/11137012/cb1e3aee1932/41419_2024_6766_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b5c/11137012/cb1e3aee1932/41419_2024_6766_Fig1_HTML.jpg

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本文引用的文献

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The roles of ferroptosis in cancer: Tumor suppression, tumor microenvironment, and therapeutic interventions.铁死亡在癌症中的作用:肿瘤抑制、肿瘤微环境和治疗干预。
Cancer Cell. 2024 Apr 8;42(4):513-534. doi: 10.1016/j.ccell.2024.03.011.
2
Programming a Ferroptosis-to-Apoptosis Transition Landscape Revealed Ferroptosis Biomarkers and Repressors for Cancer Therapy.编程铁死亡到细胞凋亡的转变景观揭示了铁死亡生物标志物和抑制剂用于癌症治疗。
Adv Sci (Weinh). 2024 May;11(17):e2307263. doi: 10.1002/advs.202307263. Epub 2024 Mar 5.
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P53 together with ferroptosis: a promising strategy leaving cancer cells without escape.
P53 与铁死亡:让癌细胞无路可逃的有前途策略。
Acta Biochim Biophys Sin (Shanghai). 2024 Jan 25;56(1):1-14. doi: 10.3724/abbs.2023270.
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Ferroptosis: the emerging player in remodeling triple-negative breast cancer.铁死亡:重塑三阴性乳腺癌的新兴角色。
Front Immunol. 2023 Oct 20;14:1284057. doi: 10.3389/fimmu.2023.1284057. eCollection 2023.
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Organelle-Specific Mechanisms in Crosstalk between Apoptosis and Ferroptosis.细胞器特异性机制在细胞凋亡和铁死亡之间的串扰中。
Oxid Med Cell Longev. 2023 Jan 5;2023:3400147. doi: 10.1155/2023/3400147. eCollection 2023.
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Ferroptosis turns 10: Emerging mechanisms, physiological functions, and therapeutic applications.铁死亡研究十周年:新兴机制、生理功能与治疗应用
Cell. 2022 Jul 7;185(14):2401-2421. doi: 10.1016/j.cell.2022.06.003.
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Ferroptosis in cancer therapy: a novel approach to reversing drug resistance.铁死亡在癌症治疗中的作用:逆转耐药性的新策略
Mol Cancer. 2022 Feb 12;21(1):47. doi: 10.1186/s12943-022-01530-y.
8
Targeting ferroptosis in breast cancer.针对乳腺癌中的铁死亡
Biomark Res. 2020 Nov 5;8(1):58. doi: 10.1186/s40364-020-00230-3.
9
Synthetic lethal combination targeting BET uncovered intrinsic susceptibility of TNBC to ferroptosis.靶向BET的合成致死组合揭示了三阴性乳腺癌对铁死亡的内在易感性。
Sci Adv. 2020 Aug 21;6(34). doi: 10.1126/sciadv.aba8968. Print 2020 Aug.
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Targeted therapy and drug resistance in triple-negative breast cancer: the EGFR axis.三阴性乳腺癌的靶向治疗和耐药性:EGFR 轴。
Biochem Soc Trans. 2020 Apr 29;48(2):657-665. doi: 10.1042/BST20191055.