Regulating ferroptosis by non-coding RNAs in hepatocellular carcinoma

IF 4.9 2区 生物学 Q1 BIOLOGY Biology Direct Pub Date : 2024-09-12 DOI:10.1186/s13062-024-00530-w
Lijie Sun, Hongfei Cao, Yanzhe Wang, Hongquan Wang
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Abstract

Ferroptosis, a unique type of regulated cell death plays a vital role in inhibiting tumour malignancy and has presented new opportunities for treatment of therapy in hepatocellular carcinoma. Accumulating studies indicate that epigenetic modifications by non-coding RNAs, including microRNAs, long noncoding RNAs, and circular RNAs, can determine cancer cell vulnerability to ferroptosis in HCC. The present review first summarize the updated core molecular mechanisms of ferroptosis. We then provide a concised overview of epigenetic modification of ferroptosis in HCC. Finally, we review the recent progress in understanding of the ncRNA-mediated regulated mechanisms on ferroptosis in HCC. The review will promote our understanding of the ncRNA-mediated epigenetic regulatory mechanisms modulating ferroptosis in malignancy of HCC, highlighting a novel strategies for treatment of HCC through targeting ncRNA-ferroptosis axis.
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肝细胞癌中的非编码 RNA 对铁突变的调控
铁突变是一种独特的调节性细胞死亡类型,在抑制肿瘤恶变方面发挥着重要作用,并为肝细胞癌的治疗提供了新的机会。不断积累的研究表明,非编码 RNA(包括 microRNA、长非编码 RNA 和环状 RNA)的表观遗传学修饰可决定 HCC 中癌细胞对铁突变的易感性。本综述首先总结了最新的铁变态反应核心分子机制。然后,我们简明扼要地概述了 HCC 中铁细胞凋亡的表观遗传修饰。最后,我们回顾了最近在了解 ncRNA 介导的 HCC 铁凋亡调控机制方面取得的进展。这篇综述将促进我们对 ncRNA 介导的表观遗传调控机制在 HCC 恶性肿瘤中调节铁凋亡的理解,并强调了通过靶向 ncRNA- 铁凋亡轴治疗 HCC 的新策略。
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来源期刊
Biology Direct
Biology Direct 生物-生物学
CiteScore
6.40
自引率
10.90%
发文量
32
审稿时长
7 months
期刊介绍: Biology Direct serves the life science research community as an open access, peer-reviewed online journal, providing authors and readers with an alternative to the traditional model of peer review. Biology Direct considers original research articles, hypotheses, comments, discovery notes and reviews in subject areas currently identified as those most conducive to the open review approach, primarily those with a significant non-experimental component.
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