Ferroptosis, necroptosis and cuproptosis: Novel forms of regulated cell death in diabetic cardiomyopathy

被引:22
作者
Ke, Dan [1 ]
Zhang, Zhen [2 ,3 ]
Liu, Jieting [1 ,2 ]
Chen, Peijian [1 ,2 ]
Li, Jialing [1 ]
Sun, Xinhai [4 ]
Chu, Yanhui [1 ,2 ]
Li, Luxin [1 ,2 ]
机构
[1] Mudanjiang Med Univ, Coll Life Sci, Mudanjiang, Peoples R China
[2] Mudanjiang Med Univ, Heilongjiang Key Lab Antifibrosis Biotherapy, Mudanjiang, Peoples R China
[3] Mudanjiang Med Univ, Sch Clin Med Coll 1, Mudanjiang, Peoples R China
[4] Fujian Med Univ, Union Hosp, Dept Thorac Surg, Fuzhou, Peoples R China
关键词
diabetic cardiomyopathy; ferroptosis; necroptosis; cuproptosis; regulatory cell death; MOUSE MODEL; OXIDATIVE STRESS; HEART-FAILURE; FATTY-ACIDS; APOPTOSIS; COPPER; IRON; MECHANISMS; METABOLISM; MITOCHONDRIA;
D O I
10.3389/fcvm.2023.1135723
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diabetes is a common chronic metabolic disease, and its incidence continues to increase year after year. Diabetic patients mainly die from various complications, with the most common being diabetic cardiomyopathy. However, the detection rate of diabetic cardiomyopathy is low in clinical practice, and targeted treatment is lacking. Recently, a large number of studies have confirmed that myocardial cell death in diabetic cardiomyopathy involves pyroptosis, apoptosis, necrosis, ferroptosis, necroptosis, cuproptosis, cellular burial, and other processes. Most importantly, numerous animal studies have shown that the onset and progression of diabetic cardiomyopathy can be mitigated by inhibiting these regulatory cell death processes, such as by utilizing inhibitors, chelators, or genetic manipulation. Therefore, we review the role of ferroptosis, necroptosis, and cuproptosis, three novel forms of cell death in diabetic cardiomyopathy, searching for possible targets, and analyzing the corresponding therapeutic approaches to these targets.
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页数:13
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