心脏毒性
基因敲除
阿霉素
小干扰RNA
癌症研究
污渍
化学
细胞生物学
分子生物学
细胞凋亡
药理学
生物
转染
医学
内科学
生物化学
毒性
化疗
基因
有机化学
作者
Dan Liu,Xiaoli Cheng,Han-Lin Wu,Haixu Song,Yuxin Bu,Jing Wang,Xiaolin Zhang,Chenghui Yan,Yaling Han
出处
期刊:Redox biology
[Elsevier]
日期:2024-07-29
卷期号:75: 103293-103293
标识
DOI:10.1016/j.redox.2024.103293
摘要
Doxorubicin (DOX)-induced cardiotoxicity limits the application of DOX in cancer patients. Currently, there is no effective prevention or treatment for DOX-induced cardiotoxicity. The cellular repressor of E1A-stimulated genes (CREG1) is a cardioprotective factor that plays an important role in the maintenance of cardiomyocytes differentiation and homeostasis. However, the role and mechanism of CREG1 in DOX-induced cardiotoxicity has not yet been elucidated.
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