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铁死亡及其在人类疾病中的潜在作用。

Ferroptosis and Its Potential Role in Human Diseases.

作者信息

Han Chu, Liu Yuanyuan, Dai Rongji, Ismail Nafissa, Su Weijun, Li Bo

机构信息

School of Chemistry and Chemical Engineering, Beijing Institute of Technology, Beijing, China.

Advanced Research Institute of Multidisciplinary Science, Beijing Institute of Technology, Beijing, China.

出版信息

Front Pharmacol. 2020 Mar 17;11:239. doi: 10.3389/fphar.2020.00239. eCollection 2020.

Abstract

Ferroptosis is a novel regulated cell death pattern discovered when studying the mechanism of erastin-killing RAS mutant tumor cells in 2012. It is an iron-dependent programmed cell death pathway mainly caused by an increased redox imbalance but with distinct biological and morphology characteristics when compared to other known cell death patterns. Ferroptosis is associated with various diseases including acute kidney injury, cancer, and cardiovascular, neurodegenerative, and hepatic diseases. Moreover, activation or inhibition of ferroptosis using a variety of ferroptosis initiators and inhibitors can modulate disease progression in animal models. In this review, we provide a comprehensive analysis of the characteristics of ferroptosis, its initiators and inhibitors, and the potential role of its main metabolic pathways in the treatment and prevention of various diseased states. We end the review with the current knowledge gaps in this area to provide direction for future research on ferroptosis.

摘要

铁死亡是2012年在研究埃拉斯汀杀死RAS突变肿瘤细胞机制时发现的一种新型调控性细胞死亡模式。它是一种铁依赖性程序性细胞死亡途径,主要由氧化还原失衡加剧引起,但与其他已知细胞死亡模式相比具有独特的生物学和形态学特征。铁死亡与多种疾病相关,包括急性肾损伤、癌症以及心血管、神经退行性和肝脏疾病。此外,使用多种铁死亡诱导剂和抑制剂激活或抑制铁死亡可以调节动物模型中的疾病进展。在本综述中,我们对铁死亡的特征、其诱导剂和抑制剂以及其主要代谢途径在各种疾病状态的治疗和预防中的潜在作用进行了全面分析。我们以该领域目前的知识空白结束本综述,为铁死亡的未来研究提供方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1aa/7090218/9b55071781c6/fphar-11-00239-g001.jpg

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