Targeting DNA damage response in cardiovascular diseases: from pathophysiology to therapeutic implications

被引:25
|
作者
Wu, Lin [1 ]
Sowers, James R. [2 ]
Zhang, Yingmei [1 ]
Ren, Jun [1 ,3 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Shanghai Inst Cardiovasc Dis, Dept Cardiol, Shanghai 200032, Peoples R China
[2] Univ Missouri, Diabet & Cardiovasc Res Ctr, Columbia, MO 65212 USA
[3] Univ Washington, Dept Lab Med & Pathol, Seattle, WA 98195 USA
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
Cardiovascular disease; DNA damage; DNA damage response; DNA repair; Therapeutics; SMOOTH-MUSCLE-CELLS; HEART ISCHAEMIA/REPERFUSION INJURY; PAROXYSMAL ATRIAL-FIBRILLATION; DOXORUBICIN-INDUCED APOPTOSIS; BASE-EXCISION-REPAIR; E-DEFICIENT MICE; POLY(ADP-RIBOSE) POLYMERASE; OXIDATIVE-STRESS; MYOCARDIAL-INFARCTION; ENDOTHELIAL DYSFUNCTION;
D O I
10.1093/cvr/cvac080
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cardiovascular diseases (CVDs) arise from a complex interplay among genomic, proteomic, and metabolomic abnormalities. Emerging evidence has recently consolidated the presence of robust DNA damage in a variety of cardiovascular disorders. DNA damage triggers a series of cellular responses termed DNA damage response (DDR) including detection of DNA lesions, cell cycle arrest, DNA repair, cellular senescence, and apoptosis, in all organ systems including hearts and vasculature. Although transient DDR in response to temporary DNA damage can be beneficial for cardiovascular function, persistent activation of DDR promotes the onset and development of CVDs. Moreover, therapeutic interventions that target DNA damage and DDR have the potential to attenuate cardiovascular dysfunction and improve disease outcome. In this review, we will discuss molecular mechanisms of DNA damage and repair in the onset and development of CVDs, and explore how DDR in specific cardiac cell types contributes to CVDs. Moreover, we will highlight the latest advances regarding the potential therapeutic strategies targeting DNA damage signalling in CVDs.
引用
收藏
页码:691 / 709
页数:19
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