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线粒体靶向小分子有效预防多柔比星所致心脏毒性。

Mitochondria-Targeting Small Molecules Effectively Prevent Cardiotoxicity Induced by Doxorubicin.

机构信息

Department of Bioengineering, Zhuhai Campus of Zunyi Medical University, Zhuhai 519041, China.

School of Life Sciences, Shandong University of Technology, Zibo 255000, China.

出版信息

Molecules. 2018 Jun 19;23(6):1486. doi: 10.3390/molecules23061486.

Abstract

Doxorubicin (Dox) is a chemotherapeutic agent widely used for the treatment of numerous cancers. However, the clinical use of Dox is limited by its unwanted cardiotoxicity. Mitochondrial dysfunction has been associated with Dox-induced cardiotoxicity. To mitigate Dox-related cardiotoxicity, considerable successful examples of a variety of small molecules that target mitochondria to modulate Dox-induced cardiotoxicity have appeared in recent years. Here, we review the related literatures and discuss the evidence showing that mitochondria-targeting small molecules are promising cardioprotective agents against Dox-induced cardiac events.

摘要

多柔比星(Dox)是一种广泛用于治疗多种癌症的化疗药物。然而,由于其不希望出现的心脏毒性,Dox 的临床应用受到限制。线粒体功能障碍与 Dox 诱导的心脏毒性有关。为了减轻 Dox 相关的心脏毒性,近年来出现了许多针对线粒体的小分子药物,这些药物可以调节 Dox 诱导的心脏毒性,取得了相当大的成功。在这里,我们综述了相关文献,并讨论了表明靶向线粒体的小分子是对抗 Dox 诱导的心脏事件有前途的心脏保护剂的证据。

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