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铁死亡:肝细胞癌的新“猎手”

Ferroptosis: a new hunter of hepatocellular carcinoma.

作者信息

Jiang Yulang, Yu Yongxin, Pan Ziyang, Glandorff Christian, Sun Mingyu

机构信息

Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.

Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.

出版信息

Cell Death Discov. 2024 Mar 13;10(1):136. doi: 10.1038/s41420-024-01863-1.

Abstract

Ferroptosis is an iron ion-dependent, regulatory cell death modality driven by intracellular lipid peroxidation that plays a key role in the development of HCC. Studies have shown that various clinical agents (e.g., sorafenib) have ferroptosis inducer-like effects and can exert therapeutic effects by modulating different key factors in the ferroptosis pathway. This implies that targeting tumor cell ferroptosis may be a very promising strategy for tumor therapy. In this paper, we summarize the prerequisites and defense systems for the occurrence of ferroptosis and the regulatory targets of drug-mediated ferroptosis action in HCC, the differences and connections between ferroptosis and other programmed cell deaths. We aim to summarize the theoretical basis, classical inducers of ferroptosis and research progress of ferroptosis in HCC cells, clued to the treatment of HCC by regulating ferroptosis network. Further investigation of the specific mechanisms of ferroptosis and the development of hepatocellular carcinoma and interventions at different stages of hepatocellular carcinoma will help us to deepen our understanding of hepatocellular carcinoma, with a view to providing new and more precise preventive as well as therapeutic measures for patients.

摘要

铁死亡是一种由细胞内脂质过氧化驱动的铁离子依赖性调节性细胞死亡方式,在肝癌发生发展中起关键作用。研究表明,多种临床药物(如索拉非尼)具有类铁死亡诱导剂作用,可通过调节铁死亡途径中的不同关键因子发挥治疗作用。这意味着靶向肿瘤细胞铁死亡可能是一种非常有前景的肿瘤治疗策略。在本文中,我们总结了铁死亡发生的前提条件和防御系统、肝癌中药物介导铁死亡作用的调控靶点、铁死亡与其他程序性细胞死亡之间的差异和联系。我们旨在总结铁死亡的理论基础、经典诱导剂以及肝癌细胞中铁死亡的研究进展,为通过调节铁死亡网络治疗肝癌提供线索。进一步研究铁死亡的具体机制、肝癌的发生发展以及在肝癌不同阶段的干预措施,将有助于我们加深对肝癌的理解,以期为患者提供新的、更精准的预防和治疗措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/452e/10937674/da2f1b4da1ed/41420_2024_1863_Fig1_HTML.jpg

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