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Programmed death of cardiomyocytes in cardiovascular disease and new therapeutic approaches. | LitMetric

Programmed death of cardiomyocytes in cardiovascular disease and new therapeutic approaches.

Pharmacol Res

Department of Cardiology, the First Hospital of China Medical University, 155 Nanjing North Street, Heping District, Shenyang, Liaoning 110001, People's Republic of China; Institute of health sciences, China medical university, 77 Puhe Road, Shenbei New District, Shenyang, Liaoning 110001, People's Republic of China. Electronic address:

Published: August 2024

AI Article Synopsis

  • * Cardiomyocyte death is influenced by various programmed cell death (PCD) pathways, and abnormalities in these processes can lead to different CVDs.
  • * The review explores the mechanisms behind cardiomyocyte death and highlights potential drug therapies that aim to target and inhibit PCD to treat cardiovascular diseases.

Article Abstract

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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Source
http://dx.doi.org/10.1016/j.phrs.2024.107281DOI Listing

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