糖尿病
医学
细胞凋亡
生物信息学
重症监护医学
发病机制
程序性细胞死亡
内科学
生物
内分泌学
遗传学
作者
Jiahui He,Zhangwang Li,Panpan Xia,Ao Shi,Xinxi FuChen,Jing Zhang,Peng Yu
标识
DOI:10.1016/j.molmet.2022.101470
摘要
With long-term metabolic malfunction, diabetes can cause serious damage to whole-body tissue and organs, resulting in a variety of complications. Therefore, it is particularly important to further explore the pathogenesis of diabetes complications and develop drugs for prevention and treatment. In recent years, different from apoptosis and necrosis, ferroptosis has been recognized as a new regulatory mode of cell death and involves the regulation of nuclear receptor coactivator 4 (NCOA4)-mediated ferritinophagy. Evidence shows that ferroptosis and ferritinophagy play a significant role in the occurrence and development of diabetes complications.
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