Division of Cardiology, Department of Internal Medicine, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Cardiac Electrophysiology Research and Training Center, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
J Cell Mol Med. 2020 Jun;24(12):6534-6557. doi: 10.1111/jcmm.15305. Epub 2020 Apr 26.
Anthracyclines is an effective chemotherapeutic treatment used for many types of cancer. However, high cumulative dosage of anthracyclines leads to cardiac toxicity and heart failure. Dysregulation of mitochondrial dynamics and function are major pathways driving this toxicity. Several pharmacological and non-pharmacological interventions aiming to attenuate cardiac toxicity by targeting mitochondrial dynamics and function have shown beneficial effects in cell and animal models. However, in clinical practice, there is currently no standard therapy for the prevention of anthracycline-induced cardiotoxicity. This review summarizes current reports on the impact of anthracyclines on cardiac mitochondrial dynamics and mitochondrial function and potential interventions targeting these pathways. The roles of mitochondrial dynamics and mitochondrial function in the development of anthracycline-induced cardiotoxicity should provide insights in devising novel strategies to attenuate the cardiac toxicity induced by anthracyclines.
蒽环类药物是一种有效的化疗药物,用于多种癌症的治疗。然而,高累积剂量的蒽环类药物会导致心脏毒性和心力衰竭。线粒体动力学和功能的失调是导致这种毒性的主要途径。一些旨在通过靶向线粒体动力学和功能来减轻心脏毒性的药理学和非药理学干预措施在细胞和动物模型中显示出了有益的效果。然而,在临床实践中,目前还没有预防蒽环类药物引起的心脏毒性的标准疗法。本综述总结了目前关于蒽环类药物对心脏线粒体动力学和线粒体功能的影响以及针对这些途径的潜在干预措施的报告。线粒体动力学和线粒体功能在蒽环类药物诱导的心脏毒性发展中的作用为设计减轻蒽环类药物引起的心脏毒性的新策略提供了思路。