过去、现在和未来心血管疾病中的铁蛋白沉积机制和调控。

IF 5.3 2区 医学 Q2 CELL BIOLOGY
Wenxi Fang, Saiyang Xie, Wei Deng
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引用次数: 0

摘要

心血管疾病(CVD)是危害人类健康的主要疾病,其风险因素导致高发病率和高住院率。细胞死亡是心血管疾病最重要的病理生理机制。作为细胞死亡机制之一,铁突变是一种新的调控细胞死亡(RCD)形式,广泛参与心血管疾病(如心肌梗死、心脏移植、动脉粥样硬化、心力衰竭、缺血再灌注损伤、心房颤动、心肌病(辐射性心肌病)、心肌梗死)的发生、心肌病(辐射诱导的心肌病、糖尿病心肌病、败血症诱导的心肌病、多柔比星诱导的心肌病、铁过载心肌病和肥厚性心肌病)和肺动脉高压),涉及铁调节、代谢机制和脂质过氧化。本文综述了近年来关于铁变态反应的机制、调控及其与心血管疾病发生和治疗关系的研究,旨在通过阐明心血管疾病研究的最新进展,为心血管疾病的临床诊治提供新的思路和治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ferroptosis mechanisms and regulations in cardiovascular diseases in the past, present, and future.

Ferroptosis mechanisms and regulations in cardiovascular diseases in the past, present, and future.

Cardiovascular diseases (CVDs) are the main diseases that endanger human health, and their risk factors contribute to high morbidity and a high rate of hospitalization. Cell death is the most important pathophysiology in CVDs. As one of the cell death mechanisms, ferroptosis is a new form of regulated cell death (RCD) that broadly participates in CVDs (such as myocardial infarction, heart transplantation, atherosclerosis, heart failure, ischaemia/reperfusion (I/R) injury, atrial fibrillation, cardiomyopathy (radiation-induced cardiomyopathy, diabetes cardiomyopathy, sepsis-induced cardiac injury, doxorubicin-induced cardiac injury, iron overload cardiomyopathy, and hypertrophic cardiomyopathy), and pulmonary arterial hypertension), involving in iron regulation, metabolic mechanism and lipid peroxidation. This article reviews recent research on the mechanism and regulation of ferroptosis and its relationship with the occurrence and treatment of CVDs, aiming to provide new ideas and treatment targets for the clinical diagnosis and treatment of CVDs by clarifying the latest progress in CVDs research.

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来源期刊
Cell Biology and Toxicology
Cell Biology and Toxicology 生物-毒理学
CiteScore
9.90
自引率
4.90%
发文量
101
审稿时长
>12 weeks
期刊介绍: Cell Biology and Toxicology (CBT) is an international journal focused on clinical and translational research with an emphasis on molecular and cell biology, genetic and epigenetic heterogeneity, drug discovery and development, and molecular pharmacology and toxicology. CBT has a disease-specific scope prioritizing publications on gene and protein-based regulation, intracellular signaling pathway dysfunction, cell type-specific function, and systems in biomedicine in drug discovery and development. CBT publishes original articles with outstanding, innovative and significant findings, important reviews on recent research advances and issues of high current interest, opinion articles of leading edge science, and rapid communication or reports, on molecular mechanisms and therapies in diseases.
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