疾病
氧化应激
脂质过氧化
程序性细胞死亡
医学
糖尿病
细胞
GPX4
细胞代谢
纤维化
肾
氧化损伤
癌症研究
新陈代谢
生物信息学
药理学
细胞凋亡
生物
内科学
生物化学
内分泌学
谷胱甘肽过氧化物酶
过氧化氢酶
作者
Fangxin Mu,Ping Luo,Yuexin Zhu,Ping Nie,Bing Li,Xue Bai
摘要
ABSTRACT Diabetic kidney disease (DKD) is a major diabetic microvascular complication that still lacks effective therapeutic drugs. Ferroptosis is a recently identified form of programmed cell death that is triggered by iron overload. It is characterized by unrestricted lipid peroxidation and subsequent membrane damage and is found in various diseases. Accumulating evidence has highlighted the crucial roles of iron overload and ferroptosis in DKD. Here, we review iron metabolism and the biology of ferroptosis. The role of aberrant ferroptosis in inducing diverse renal intrinsic cell death, oxidative stress, and renal fibrosis in DKD is summarized, and we elaborate on critical regulatory factors related to ferroptosis in DKD. Finally, we focused on the significance of ferroptosis in the treatment of DKD and highlight recent data regarding the novel activities of some drugs as ferroptosis inhibitors in DKD, aiming to provide new research targets and treatment strategies on DKD.
科研通智能强力驱动
Strongly Powered by AbleSci AI