实用肿瘤学杂志 ›› 2025, Vol. 39 ›› Issue (3): 256-261.doi: 10.11904/j.issn.1002-3070.2025.03.012

• 综述 • 上一篇    下一篇

非编码RNA调控铁死亡介导肝细胞癌索拉非尼耐药的研究进展

朱磊1 综述, 郝丹丹2 审校   

  1. 1.赤峰学院附属医院检验科(赤峰 024005);
    2赤峰学院医学部基础医学院生理学教研室
  • 收稿日期:2024-08-09 修回日期:2025-04-02 出版日期:2025-06-28 发布日期:2025-07-02
  • 通讯作者: 郝丹丹,E-mail:hdd2011yx@163.com
  • 作者简介:朱磊,男,(1989—),学士,主管检验技师,从事发现肿瘤生物标志物的研究。
  • 基金资助:
    内蒙古自治区自然科学基金(编号:2022MS08032)

Research progress on non-coding RNAs in the regulation of ferroptosis mediated sorafenib resistance in hepatocellular carcinoma

ZHU Lei1, HAO Dandan2   

  1. 1. Department of Clinical Laboratory,The Affiliated Hospital of Chifeng University,Chifeng 024005,China;
    2. Department of Physiology,Medical college,Chifeng University
  • Received:2024-08-09 Revised:2025-04-02 Online:2025-06-28 Published:2025-07-02

摘要: 铁死亡是一种由铁离子介导的脂质过氧化驱动的非凋亡性细胞程序性死亡,与多种肿瘤的发生发展密切相关。近年来研究表明,非编码RNA(non-coding RNA,ncRNA)可通过调控铁死亡通路影响肿瘤耐药进程。本文总结了ncRNAs通过铁死亡调控肝细胞癌(hepatocellular carcinoma,HCC)索拉非尼(sorafenib)耐药的分子机制,重点阐述微RNA(microRNA,miRNA)、长链非编码RNA(long noncoding RNA,lncRNA)和环状RNA(circular RNA,circRNA)等不同亚型ncRNA在其中的调控作用。本文有助于深入解析ncRNA通过铁死亡途径介导HCC索拉非尼耐药的关键分子机制,同时为未来探索HCC新型诊断生物标志物及治疗靶点提供理论依据。

关键词: 肝细胞癌, 非编码RNA, 铁死亡, 索拉非尼, 生物标志物

Abstract: Ferroptosis is a non-apoptotic programmed cell death driven by iron ion-mediated lipid peroxidation,which is closely related to the occurrence and development of various tumors.In recent years,many studies have shown that non-coding RNA(ncRNA)can affect tumor drug resistance by regulating the ferroptosis pathway.This article summarizes the molecular mechanisms of ncRNAs regulating sorafenib resistance in hepatocellular carcinoma(HCC)through ferroptosis,with a focus on the regulatory roles of different ncRNA subtypes such as microRNA(miRNA),long noncoding RNA(lncRNA),and circular RNA(circRNA).The article not only contributes to a deeper analysis of the key molecular mechanisms by which ncRNA mediate sorafenib resistance in HCC through ferroptosis pathways,but also provides a theoretical basis for exploring novel diagnostic biomarkers and therapeutic targets for HCC in the future.

Key words: Hepatocellular carcinoma, Non-coding RNA, Ferroptosis, Sorafenib, Biomarkers

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