Epigenetic regulation of targeted ferroptosis: A new strategy for drug development

被引:0
|
作者
Ouyang, Shengli [1 ]
Zeng, Zeyao [1 ]
He, Jieyi [1 ]
Luo, Lianxiang [2 ]
机构
[1] Guangdong Med Univ, Clin Coll 1, Zhanjiang 524023, Guangdong, Peoples R China
[2] Guangdong Med Univ, Marine Biomed Res Inst Guangdong Zhanjiang, Sch Ocean & Trop Med, Zhanjiang 524023, Guangdong, Peoples R China
关键词
Treatment strategies; Epigenetics; Ferroptosis; Epigenetic modifiers; HEPATOCELLULAR-CARCINOMA; INHIBITS FERROPTOSIS; SIGNALING PATHWAY; GENE-EXPRESSION; RNA METHYLATION; CELL-DEATH; CANCER; MECHANISMS; ANTIOXIDANT; METABOLISM;
D O I
10.1016/j.jpha.2024.101012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ferroptosis is a newly discovered form of cell death that is influenced by iron levels and is triggered by cellular metabolism and excessive lipid peroxidation. Epigenetic regulation plays a crucial role in the development and progression of diseases, making it essential to understand these mechanisms in order to identify potential targets for drug development and clinical treatment. The intersection of ferroptosis and epigenetics has opened up new avenues for research in drug development, offering innovative strategies for combating diseases. Recent studies have shown that epigenetic modifications can impact pathways related to ferroptosis, potentially leading to organ dysfunction. Despite the increasing focus on this relationship, the role of epigenetic regulation in drug development remains largely unexplored. This article explores current research on the interplay between epigenetic regulation and ferroptosis, delving into their regulatory mechanisms and discussing the effects of existing epigenetic modification regulators on diseases. Additionally, we highlight ongoing research on epigenetic factors involved in targeting ferroptosis in cancer, providing new insights for the development of cancer treatments. (c) 2024 The Authors. Published by Elsevier B.V. on behalf of Xi'an Jiaotong University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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页数:18
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