脱铁性贫血的发病机制及其相关疾病。

IF 6.3 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular biomedicine Pub Date : 2023-10-16 DOI:10.1186/s43556-023-00142-2
Shijian Feng, Dan Tang, Yichang Wang, Xiang Li, Hui Bao, Chengbing Tang, Xiuju Dong, Xinna Li, Qinxue Yang, Yun Yan, Zhijie Yin, Tiantian Shang, Kaixuan Zheng, Xiaofang Huang, Zuheng Wei, Kunjie Wang, Shiqian Qi
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摘要

脱铁症是一种以铁介导的脂质过氧化物积累为特征的细胞死亡调控形式,为深入研究细胞代谢、氧化应激和疾病病理学的交叉提供了一条新的途径。我们目睹了人们对脱铁性贫血越来越着迷,这归因于它在各种生理和病理条件下的关键作用,包括发育过程、代谢动力学、致癌途径、神经退行性级联反应和创伤性组织损伤。通过揭示控制脱铁性贫血的分子机制、关键贡献者、复杂的信号传导渠道和调控网络的复杂基础,研究人员旨在弥合这种独特的细胞死亡模式的复杂性与其对健康和疾病的多方面影响之间的差距。鉴于脱铁症研究的快速发展,我们对脱铁症在人类疾病起源和进展中的广泛意义进行了全面的综述。这篇综述最后对精心设计的抑制或促进脱铁性贫血的潜在治疗方法进行了仔细分析。此外,我们简要总结了在各种疾病中靶向脱铁性贫血的潜在治疗靶点和化合物。这一关键方面强调了操纵脱铁性贫血作为一种治疗策略的新兴可能性。总之,这篇综述丰富了研究人员和从业者的见解,同时提高了对脱铁性贫血及其潜在翻译效用的理解。通过揭示基本过程和研究治疗可能性,这篇综述为科学家和医生提供了重要的资源,有助于深入了解脱铁性贫血及其在各种疾病情况下的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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The mechanism of ferroptosis and its related diseases.

Ferroptosis, a regulated form of cellular death characterized by the iron-mediated accumulation of lipid peroxides, provides a novel avenue for delving into the intersection of cellular metabolism, oxidative stress, and disease pathology. We have witnessed a mounting fascination with ferroptosis, attributed to its pivotal roles across diverse physiological and pathological conditions including developmental processes, metabolic dynamics, oncogenic pathways, neurodegenerative cascades, and traumatic tissue injuries. By unraveling the intricate underpinnings of the molecular machinery, pivotal contributors, intricate signaling conduits, and regulatory networks governing ferroptosis, researchers aim to bridge the gap between the intricacies of this unique mode of cellular death and its multifaceted implications for health and disease. In light of the rapidly advancing landscape of ferroptosis research, we present a comprehensive review aiming at the extensive implications of ferroptosis in the origins and progress of human diseases. This review concludes with a careful analysis of potential treatment approaches carefully designed to either inhibit or promote ferroptosis. Additionally, we have succinctly summarized the potential therapeutic targets and compounds that hold promise in targeting ferroptosis within various diseases. This pivotal facet underscores the burgeoning possibilities for manipulating ferroptosis as a therapeutic strategy. In summary, this review enriched the insights of both investigators and practitioners, while fostering an elevated comprehension of ferroptosis and its latent translational utilities. By revealing the basic processes and investigating treatment possibilities, this review provides a crucial resource for scientists and medical practitioners, aiding in a deep understanding of ferroptosis and its effects in various disease situations.

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CiteScore
6.30
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审稿时长
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