上睑下垂
坏死性下垂
程序性细胞死亡
自噬
疾病
死因
医学
细胞凋亡
生物信息学
生物
病理
生物化学
作者
Kexin Cai,Haoyue Jiang,Yuanming Zou,Chunyu Song,Kexin Cao,Shuxian Chen,Yanjiao Wu,Zhaobo Zhang,Danxi Geng,Naijin Zhang,Bo Liu,Guozhe Sun,Man Tang,Li Zhao,Yixiao Zhang,Yingxian Sun,Ying Zhang
标识
DOI:10.1016/j.phrs.2024.107281
摘要
Cardiovascular diseases (CVDs) have a complex pathogenesis and pose a major threat to human health. Cardiomyocytes have a low regenerative capacity, and their death is a key factor in the morbidity and mortality of many CVDs. Cardiomyocyte death can be regulated by specific signaling pathways known as programmed cell death (PCD), including apoptosis, necroptosis, autophagy, pyroptosis, and ferroptosis, etc. Abnormalities in PCD can lead to the development of a variety of cardiovascular diseases, and there are also molecular-level interconnections between different PCD pathways under the same cardiovascular disease model. Currently, the link between programmed cell death in cardiomyocytes and cardiovascular disease is not fully understood. This review describes the molecular mechanisms of programmed death and the impact of cardiomyocyte death on cardiovascular disease development. Emphasis is placed on a summary of drugs and potential therapeutic approaches that can be used to treat cardiovascular disease by targeting and blocking programmed cell death in cardiomyocytes.
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