Luu Albert Z, Chowdhury Biswajit, Al-Omran Mohammed, Teoh Hwee, Hess David A, Verma Subodh
Division of Cardiac Surgery, Keenan Research Centre for Biomedical Science, St. Michael's Hospital, Toronto, Ontario, Canada.
Department of Pharmacology and Toxicology, University of Toronto, Toronto, Ontario, Canada.
JACC Basic Transl Sci. 2018 Dec 31;3(6):861-870. doi: 10.1016/j.jacbts.2018.06.005. eCollection 2018 Dec.
The clinical use of doxorubicin in cancer is limited by cardiotoxic effects that can lead to heart failure. Whereas earlier work focused on the direct impact of doxorubicin on cardiomyocytes, recent studies have turned to the endothelium, because doxorubicin-damaged endothelial cells can trigger the development and progression of cardiomyopathy by decreasing the release and activity of key endothelial factors and inducing endothelial cell death. Thus, the endothelium represents a novel target for improving the detection, management, and prevention of doxorubicin-induced cardiomyopathy.
阿霉素在癌症临床应用中受到心脏毒性作用的限制,这种毒性作用可导致心力衰竭。早期研究聚焦于阿霉素对心肌细胞的直接影响,而近期研究则转向了内皮细胞,因为阿霉素损伤的内皮细胞可通过减少关键内皮因子的释放和活性以及诱导内皮细胞死亡,引发心肌病的发展和进展。因此,内皮细胞是改善阿霉素诱导的心肌病检测、管理和预防的新靶点。