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肝细胞癌中铁死亡研究的最新进展。

Current Progress of Ferroptosis Study in Hepatocellular Carcinoma.

机构信息

Department of Clinical Laboratory, the First Affiliated Hospital of Anhui Medical University, Shushan District, No. 218 Jixi Road, Hefei, 230032, Anhui, China.

Department of Pharmacology and Chemical Biology, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China.

出版信息

Int J Biol Sci. 2024 Jul 1;20(9):3621-3637. doi: 10.7150/ijbs.96014. eCollection 2024.

Abstract

Ferroptosis, an emerging type of programmed cell death, is initiated by iron-dependent and excessive ROS-mediated lipid peroxidation, which eventually leads to plasma membrane rupture and cell death. Many canonical signalling pathways and biological processes are involved in ferroptosis. Furthermore, cancer cells are more susceptible to ferroptosis due to the high load of ROS and unique metabolic characteristics, including iron requirements. Recent investigations have revealed that ferroptosis plays a crucial role in the progression of tumours, especially HCC. Specifically, the induction of ferroptosis can not only inhibit the growth of hepatoma cells, thereby reversing tumorigenesis, but also improves the efficacy of immunotherapy and enhances the antitumour immune response. Therefore, triggering ferroptosis has become a new therapeutic strategy for cancer therapy. In this review, we summarize the characteristics of ferroptosis based on its underlying mechanism and role in HCC and provide possible therapeutic applications.

摘要

铁死亡是一种新的细胞程序性死亡方式,由铁依赖性和过量的 ROS 介导的脂质过氧化引起,最终导致细胞膜破裂和细胞死亡。许多经典的信号通路和生物学过程都参与了铁死亡。此外,由于 ROS 负荷高和独特的代谢特征,包括铁需求,癌细胞更容易受到铁死亡的影响。最近的研究表明,铁死亡在肿瘤的进展中起着至关重要的作用,特别是 HCC。具体来说,诱导铁死亡不仅可以抑制肝癌细胞的生长,从而逆转肿瘤发生,还可以提高免疫治疗的疗效,并增强抗肿瘤免疫反应。因此,触发铁死亡已成为癌症治疗的一种新的治疗策略。在这篇综述中,我们总结了铁死亡的特征,基于其在 HCC 中的潜在机制和作用,并提供了可能的治疗应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4b3/11234204/6862b2f8695b/ijbsv20p3621g001.jpg

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