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多柔比星诱导心脏毒性中的调控细胞死亡途径。

Regulated cell death pathways in doxorubicin-induced cardiotoxicity.

机构信息

Centre for Heart Lung Innovation, Department of Medicine, University of British Columbia, Vancouver, BC, Canada.

Department of Medicine, University of British Columbia, Vancouver, BC, Canada.

出版信息

Cell Death Dis. 2021 Apr 1;12(4):339. doi: 10.1038/s41419-021-03614-x.

DOI:10.1038/s41419-021-03614-x
PMID:33795647
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8017015/
Abstract

Doxorubicin is a chemotherapeutic drug used for the treatment of various malignancies; however, patients can experience cardiotoxic effects and this has limited the use of this potent drug. The mechanisms by which doxorubicin kills cardiomyocytes has been elusive and despite extensive research the exact mechanisms remain unknown. This review focuses on recent advances in our understanding of doxorubicin induced regulated cardiomyocyte death pathways including autophagy, ferroptosis, necroptosis, pyroptosis and apoptosis. Understanding the mechanisms by which doxorubicin leads to cardiomyocyte death may help identify novel therapeutic agents and lead to more targeted approaches to cardiotoxicity testing.

摘要

多柔比星是一种用于治疗各种恶性肿瘤的化疗药物;然而,患者可能会出现心脏毒性作用,这限制了这种强效药物的使用。多柔比星杀死心肌细胞的机制一直难以捉摸,尽管进行了广泛的研究,但确切的机制仍不清楚。本综述重点介绍了我们对多柔比星诱导的调节性心肌细胞死亡途径的最新认识,包括自噬、铁死亡、坏死性凋亡、细胞焦亡和细胞凋亡。了解多柔比星导致心肌细胞死亡的机制可能有助于确定新的治疗剂,并导致更有针对性的心脏毒性测试方法。

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Cell Death Dis. 2021 Apr 1;12(4):339. doi: 10.1038/s41419-021-03614-x.
2
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Acyl-CoA thioesterase 1 prevents cardiomyocytes from Doxorubicin-induced ferroptosis via shaping the lipid composition.酰基辅酶 A 硫酯酶 1 通过塑造脂质组成预防心肌细胞蒽环类药物诱导的铁死亡。
Cell Death Dis. 2020 Sep 15;11(9):756. doi: 10.1038/s41419-020-02948-2.
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Variation in RARG increases susceptibility to doxorubicin-induced cardiotoxicity in patient specific induced pluripotent stem cell-derived cardiomyocytes.RARG 变异增加了患者特异性诱导多能干细胞衍生心肌细胞对阿霉素诱导的心脏毒性的易感性。
Sci Rep. 2020 Jun 25;10(1):10363. doi: 10.1038/s41598-020-65979-x.
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Molecular Mechanisms of Cardiomyocyte Death in Drug-Induced Cardiotoxicity.
虾青素通过减轻大鼠的线粒体分裂和自噬来减轻阿霉素诱导的心脏毒性。
Sci Rep. 2025 Sep 1;15(1):32114. doi: 10.1038/s41598-025-17253-1.
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Activation of CISD2 as a protective strategy against doxorubicin-induced cardiotoxicity.激活CISD2作为对抗阿霉素诱导的心脏毒性的一种保护策略。
Redox Biol. 2025 Aug 22;86:103840. doi: 10.1016/j.redox.2025.103840.
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Pharmaceutics. 2025 Jul 28;17(8):977. doi: 10.3390/pharmaceutics17080977.
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Medicina (Kaunas). 2025 Jul 25;61(8):1347. doi: 10.3390/medicina61081347.
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药物性心脏毒性中心肌细胞死亡的分子机制
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Life Sci. 2020 Feb 1;242:117186. doi: 10.1016/j.lfs.2019.117186. Epub 2019 Dec 17.
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Biochem Biophys Res Commun. 2020 Feb 26;523(1):140-146. doi: 10.1016/j.bbrc.2019.12.027. Epub 2019 Dec 16.
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