Underlying the Mechanisms of Doxorubicin-Induced Acute Cardiotoxicity: Oxidative Stress and Cell Death

被引:180
作者
Kong, Chun-Yan [1 ,2 ]
Guo, Zhen [1 ,2 ]
Song, Peng [1 ,2 ]
Zhang, Xin [1 ,2 ]
Yuan, Yu-Pei [1 ,2 ]
Teng, Teng [1 ,2 ]
Yan, Ling [1 ,2 ]
Tang, Qi-Zhu [1 ,2 ]
机构
[1] Wuhan Univ, Dept Cardiol, Renmin Hosp, Wuhan 430060, Peoples R China
[2] Hubei Key Lab Metab & Chron Dis, Wuhan 430060, Peoples R China
来源
INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES | 2022年 / 18卷 / 02期
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Doxorubicin; cardiotoxicity; oxidative stress; cell death; MANGANESE SUPEROXIDE-DISMUTASE; INDUCED CARDIAC DYSFUNCTION; INDUCED CARDIOMYOPATHY; NITRIC-OXIDE; ATTENUATES CARDIOTOXICITY; INDUCED HEART; MOUSE HEART; HUMAN SIR2; MITOCHONDRIAL; PROTECTS;
D O I
10.7150/ijbs.65258
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cancer is a destructive disease that causes high levels of morbidity and mortality. Doxorubicin (DOX) is a highly efficient antineoplastic chemotherapeutic drug, but its use places survivors at risk for cardiotoxicity. Many studies have demonstrated that multiple factors are involved in DOX-induced acute cardiotoxicity. Among them, oxidative stress and cell death predominate. In this review, we provide a comprehensive overview of the mechanisms underlying the source and effect of free radicals and dependent cell death pathways induced by DOX. Hence, we attempt to explain the cellular mechanisms of oxidative stress and cell death that elicit acute cardiotoxicity and provide new insights for researchers to discover potential therapeutic strategies to prevent or reverse doxorubicin-induced cardiotoxicity.
引用
收藏
页码:760 / 770
页数:11
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