靶向铁蛋白沉积:治疗动脉粥样硬化的新策略。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Yifan Zhang, Chengshi Jiang, Ning Meng
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引用次数: 0

摘要

自 2012 年报道铁蛋白沉积症以来,其在各种疾病中的应用前景受到广泛关注,最初是作为肿瘤的治疗方向。最新研究表明,铁蛋白沉积症与动脉粥样硬化的发生和发展密切相关。其主要机制是通过细胞内铁平衡、ROS 和过氧化脂质的产生和代谢以及细胞内多种信号通路影响动脉粥样硬化的发生和发展。抑制铁变态反应可有效抑制动脉粥样硬化的发展,为治疗动脉粥样硬化带来新的方向。在这篇综述中,我们讨论了嗜铁细胞增多症的机制,重点研究了嗜铁细胞增多症与动脉粥样硬化之间的关系,总结了已被广泛研究的不同类型的嗜铁细胞增多症抑制剂,并探讨了以嗜铁细胞增多症为靶点治疗动脉粥样硬化值得关注的一些问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Targeting Ferroptosis: A Novel Strategy for the Treatment of Atherosclerosis.

Since ferroptosis was reported in 2012, its application prospects in various diseases have been widely considered, initially as a treatment direction for tumors. Recent studies have shown that ferroptosis is closely related to the occurrence and development of atherosclerosis. The primary mechanism is to affect the occurrence and development of atherosclerosis through intracellular iron homeostasis, ROS and lipid peroxide production and metabolism, and a variety of intracellular signaling pathways. Inhibition of ferroptosis is effective in inhibiting the development of atherosclerosis, and it can bring a new direction for treating atherosclerosis. In this review, we discuss the mechanism of ferroptosis and focus on the relationship between ferroptosis and atherosclerosis, summarize the different types of ferroptosis inhibitors that have been widely studied, and discuss some issues worthy of attention in the treatment of atherosclerosis by targeting ferroptosis.

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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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