The true colors of autophagy in doxorubicin-induced cardiotoxicity

被引:45
|
作者
Xiao, Bin [1 ,2 ]
Hong, Lang [1 ,3 ]
Cai, Xinyong [1 ,3 ]
Mei, Songbo [1 ,2 ]
Zhang, Ping [4 ]
Shao, Liang [1 ,3 ]
机构
[1] Jiangxi Prov Peoples Hosp, Dept Cardiol, 92 Aiguo Rd, Nanchang 330006, Jiangxi, Peoples R China
[2] Nanchang Univ, Med Grad Sch, Nanchang 330006, Jiangxi, Peoples R China
[3] Jiang Xi Prov Inst Cardiovasc Dis, Nanchang 330006, Jiangxi, Peoples R China
[4] Jiangxi Prov Peoples Hosp, Dept Neurol, Nanchang 330006, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
doxorubicin; cardiotoxicity; autophagy; OXIDATIVE STRESS; TOPOISOMERASE-II; APOPTOSIS; KINASE; DEATH; INHIBITION; PATHWAYS; DEGRADATION; KEAP1-NRF2; PROTECTS;
D O I
10.3892/ol.2019.10576
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Patients with cancer receiving doxorubicin-based chemotherapy often have to stop taking the drug due to its cardiotoxicity and therefore lose out on the beneficial effects of its potent antitumor activity. Doxorubicin has been demonstrated to damage cardiomyocytes via various mechanisms, including accumulation of reactive oxygen species (ROS), DNA damage and autophagy dysfunction. The present review focuses on autophagy, describing the general process of autophagy and the controversy surrounding its role in doxorubicin-induced cardiotoxicity. In addition, the associations between autophagy and apoptosis, ROS, DNA damage and inflammatory processes are discussed. In the future, it will be useful to further elucidate the process of autophagy and reveal its association with various pathological processes to develop effective strategies of preventing doxorubicin-induced cardiotoxicity.
引用
收藏
页码:2165 / 2172
页数:8
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