Ferroptosis and iron metabolism in diabetes: Pathogenesis, associated complications, and therapeutic implications

被引:0
|
作者
Jin, Eun-Ju [1 ]
Jo, Yunju [1 ]
Wei, Shibo [1 ]
Rizzo, Manfredi [2 ,3 ]
Ryu, Dongryeol [1 ]
Gariani, Karim [4 ,5 ]
机构
[1] Gwangju Inst Sci & Technol, Dept Biomed Sci & Engn, Gwangju, South Korea
[2] Mohammed Bin Rashid Univ Med & Hlth Sci, Coll Med, Dubai, U Arab Emirates
[3] Univ Palermo, Dept Hlth Promot Sci Maternal & Infant Care Intern, Palermo, Italy
[4] Geneva Univ Hosp, Fac Med, Serv Endocrinol Diabet Nutr & Therapeut Educ, Geneva, Switzerland
[5] Univ Geneva Med Sch, Fac Med, Diabet Ctr, Geneva, Switzerland
来源
FRONTIERS IN ENDOCRINOLOGY | 2024年 / 15卷
基金
新加坡国家研究基金会;
关键词
ferroptosis; diabetes; iron; treatment; complications; HUMAN-DIPLOID FIBROBLASTS; OXIDATIVE STRESS; NRF2; PROTEIN; ACTIVATION; INHIBITION; APOPTOSIS; AUTOPHAGY; RECEPTOR; CYSTINE;
D O I
10.3389/fendo.2024.1447148
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diabetes mellitus is a complex chronic disease, considered as one of the most common metabolic disorders worldwide, posing a major threat to global public health. Ferroptosis emerges as a novel mechanism of programmed cell death, distinct from apoptosis, necrosis, and autophagy, driven by iron-dependent lipid peroxidation accumulation and GPx4 downregulation. A mounting body of evidence highlights the interconnection between iron metabolism, ferroptosis, and diabetes pathogenesis, encompassing complications like diabetic nephropathy, cardiomyopathy, and neuropathy. Moreover, ferroptosis inhibitors hold promise as potential pharmacological targets for mitigating diabetes-related complications. A better understanding of the role of ferroptosis in diabetes may lead to an improvement in global diabetes management.In this review, we delve into the intricate relationship between ferroptosis and diabetes development, exploring associated complications and current pharmacological treatments.
引用
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页数:11
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