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在病理生理条件下通过天然产物靶向铁死亡

Targeting ferroptosis by natural products in pathophysiological conditions.

作者信息

Zheng Daheng, Jin Shikai, Liu Pu-Ste, Ye Jianping, Xie Xin

机构信息

School of Life and Environmental Sciences, Shaoxing University, Shaoxing, Zhejiang, China.

Department of Biochemistry and Molecular Biology, College of Medicine, National Cheng Kung University, Tainan, Taiwan, ROC.

出版信息

Arch Toxicol. 2024 Oct;98(10):3191-3208. doi: 10.1007/s00204-024-03812-4. Epub 2024 Jul 10.

DOI:10.1007/s00204-024-03812-4
PMID:38987487
Abstract

Ferroptosis is a form of cell death that is induced by iron-mediated accumulation of lipid peroxidation. The involvement of ferroptosis in different pathophysiological conditions has offered new perspectives on potential therapeutic interventions. Natural products, which are widely recognized for their significance in drug discovery and repurposing, have shown great promise in regulating ferroptosis by targeting various ferroptosis players. In this review, we discuss the regulatory mechanisms of ferroptosis and its implications in different pathological conditions. We dissect the interactions between natural products and ferroptosis in cancer, ischemia/reperfusion, neurodegenerative diseases, acute kidney injury, liver injury, and cardiomyopathy, with an emphasis on the relevance of ferroptosis players to disease targetability.

摘要

铁死亡是一种由铁介导的脂质过氧化积累所诱导的细胞死亡形式。铁死亡参与不同的病理生理状况为潜在的治疗干预提供了新的视角。天然产物因其在药物发现和重新利用方面的重要性而被广泛认可,已显示出通过靶向各种铁死亡相关因子来调节铁死亡的巨大潜力。在本综述中,我们讨论了铁死亡的调控机制及其在不同病理状况中的意义。我们剖析了天然产物与癌症、缺血/再灌注、神经退行性疾病、急性肾损伤、肝损伤和心肌病中铁死亡之间的相互作用,重点关注铁死亡相关因子与疾病靶向性的相关性。

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本文引用的文献

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SMURF2 predisposes cancer cell toward ferroptosis in GPX4-independent manners by promoting GSTP1 degradation.SMURF2 通过促进 GSTP1 降解以 GPX4 非依赖的方式使癌细胞易于发生铁死亡。
Mol Cell. 2023 Dec 7;83(23):4352-4369.e8. doi: 10.1016/j.molcel.2023.10.042. Epub 2023 Nov 27.
2
Targeting ferroptosis with natural products in liver injury: new insights from molecular mechanisms to targeted therapies.天然产物靶向铁死亡治疗肝损伤:从分子机制到靶向治疗的新见解
Phytomedicine. 2024 Jan;122:155134. doi: 10.1016/j.phymed.2023.155134. Epub 2023 Oct 4.
3
Caffeic acid alleviates cerebral ischemic injury in rats by resisting ferroptosis via Nrf2 signaling pathway.
咖啡酸通过 Nrf2 信号通路抵抗铁死亡来减轻大鼠的脑缺血损伤。
Acta Pharmacol Sin. 2024 Feb;45(2):248-267. doi: 10.1038/s41401-023-01177-5. Epub 2023 Oct 13.
4
The interplay of miRNAs and ferroptosis in diseases related to iron overload.miRNAs 与铁过载相关疾病中铁死亡之间的相互作用。
Apoptosis. 2024 Feb;29(1-2):45-65. doi: 10.1007/s10495-023-01890-w. Epub 2023 Sep 27.
5
Mechanisms of Ferritinophagy and Ferroptosis in Diseases.铁蛋白自噬和铁死亡在疾病中的作用机制。
Mol Neurobiol. 2024 Mar;61(3):1605-1626. doi: 10.1007/s12035-023-03640-0. Epub 2023 Sep 22.
6
Therapeutic inhibition of ferroptosis in neurodegenerative disease.神经退行性疾病中铁死亡的治疗性抑制
Trends Pharmacol Sci. 2023 Oct;44(10):674-688. doi: 10.1016/j.tips.2023.07.007. Epub 2023 Aug 30.
7
Kinsenoside mitigates myocardial ischemia/reperfusion-induced ferroptosis via activation of the Akt/Nrf2/HO-1 pathway.金雀异皂苷通过激活 Akt/Nrf2/HO-1 通路减轻心肌缺血/再灌注诱导的铁死亡。
Eur J Pharmacol. 2023 Oct 5;956:175985. doi: 10.1016/j.ejphar.2023.175985. Epub 2023 Aug 10.
8
Silibinin ameliorates STING-mediated neuroinflammation via downregulation of ferroptotic damage in a sporadic Alzheimer's disease model.水飞蓟宾通过下调散发性阿尔茨海默病模型中铁死亡损伤改善 STING 介导的神经炎症。
Arch Biochem Biophys. 2023 Aug;744:109691. doi: 10.1016/j.abb.2023.109691. Epub 2023 Jul 18.
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Oleanolic acid inhibits mercury chloride induced-liver ferroptosis by regulating ROS/iron overload.齐墩果酸通过调节 ROS/铁过载抑制氯化汞诱导的肝铁死亡。
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Cyanidin-3-glucoside inhibits ferroptosis in renal tubular cells after ischemia/reperfusion injury via the AMPK pathway.矢车菊素-3-葡萄糖苷通过 AMPK 通路抑制缺血再灌注损伤后肾小管细胞中的铁死亡。
Mol Med. 2023 Apr 3;29(1):42. doi: 10.1186/s10020-023-00642-5.