脂肪性肝炎
GPX4
脂肪肝
肝硬化
酒精性肝病
过氧化脂质
慢性肝病
程序性细胞死亡
肝病
肝癌
癌症研究
机制(生物学)
脂质过氧化
肝细胞
疾病
生物
医学
谷胱甘肽过氧化物酶
生物化学
氧化应激
细胞凋亡
超氧化物歧化酶
病理
内科学
肝细胞癌
哲学
认识论
作者
Lujian Zhu,Shengnan Luo,Yin Zhu,Shiyue Tang,Chenge Li,Xiaozhi Jin,Fa-Ling Wu,Huimian Jiang,Lina Wu,Yejin Xu
摘要
Abstract: Ferroptosis is a recently identified iron-dependent form of intracellular lipid peroxide accumulation-mediated cell death. Different from other types of cell death mechanisms, it exhibits distinct biological and morphological features characterized by the loss of lipid peroxidase repair activity caused by glutathione peroxidase 4, the presence of redox-active iron, and the oxidation of phospholipids-containing polyunsaturated fatty acids. In recent years, studies have shown that ferroptosis plays a key role in various liver diseases such as alcoholic liver injury, non-alcoholic steatohepatitis, liver cirrhosis, and liver cancer. However, the mechanism of ferroptosis and its regulation on chronic liver disease are controversial among different types of cells in the liver. Herein, we summarize the current studies on mechanism of ferroptosis in chronic liver disease, aiming to outline the blueprint of ferroptosis as an effective option for chronic liver disease therapy. Keywords: ferroptosis, iron metabolism, liver disease, oxidative stress, cell death
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