He Ling, Liu Fuxiang, Li Juxiang
Department of Cardiovascular Medicine, The Second Affiliated Hospital of Nanchang University, Minde Road No. 1, Nanchang of Jiangxi, 330006, China.
Cardiovasc Toxicol. 2021 Mar;21(3):179-191. doi: 10.1007/s12012-020-09626-x. Epub 2021 Jan 12.
Doxorubicin (DOX) is the most effective and extensively used treatment for many tumors. However, its clinical use is hampered by its cardiotoxicity. DOX-induced mitochondrial dysfunction, which causes reactive oxygen species (ROS) generation, cardiomyocyte death, bioenergetic failure, and decreased cardiac function, is a very important mechanism of cardiotoxicity. These cellular processes are all linked by mitochondrial sirtuins (SIRT3-SIRT4). Mitochondrial sirtuins preserve mitochondrial function by increasing mitochondrial metabolism, inhibiting ROS generation by activating the antioxidant enzyme manganese-dependent superoxide dismutase (MnSOD), decreasing apoptosis by activating the forkhead homeobox type O (FOXO) and P53 pathways, and increasing autophagy through AMP-activated protein kinase (AMPK)/mTOR signaling. Thus, sirtuins function at the control point of many mechanisms involved in DOX-induced cardiotoxicity. In this review, we focus on the role of mitochondrial sirtuins in mitochondrial biology and DOX-induced cardiotoxicity. A further aim is to highlight other mitochondrial processes, such as autophagy (mitophagy) and mitochondrial quality control (MQC), for which the effect of mitochondrial sirtuins on cardiotoxicity is unknown.
阿霉素(DOX)是治疗多种肿瘤最有效且应用最广泛的药物。然而,其心脏毒性限制了它的临床应用。DOX诱导的线粒体功能障碍是心脏毒性的一个非常重要的机制,它会导致活性氧(ROS)生成、心肌细胞死亡、生物能量衰竭以及心脏功能下降。这些细胞过程都与线粒体去乙酰化酶(SIRT3 - SIRT4)有关。线粒体去乙酰化酶通过增强线粒体代谢、激活抗氧化酶锰依赖性超氧化物歧化酶(MnSOD)来抑制ROS生成、激活叉头框O型(FOXO)和P53通路来减少细胞凋亡以及通过AMP激活的蛋白激酶(AMPK)/雷帕霉素靶蛋白(mTOR)信号传导增强自噬,从而维持线粒体功能。因此,去乙酰化酶在DOX诱导的心脏毒性所涉及的许多机制的控制点发挥作用。在本综述中,我们聚焦于线粒体去乙酰化酶在线粒体生物学和DOX诱导的心脏毒性中的作用。另一个目的是强调其他线粒体过程,如自噬(线粒体自噬)和线粒体质量控制(MQC),目前线粒体去乙酰化酶对其心脏毒性的影响尚不清楚。