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FSP1 oxidizes NADPH to suppress ferroptosis.FSP1氧化NADPH以抑制铁死亡。
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Phase separation of FSP1 promotes ferroptosis.FSP1 的相分离促进了铁死亡。
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Cell-membrane targeting sonodynamic therapy combination with FSP1 inhibition for ferroptosis-boosted immunotherapy.细胞膜靶向声动力疗法联合FSP1抑制用于增强铁死亡的免疫治疗。
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FSP1: a key regulator of ferroptosis.FSP1:铁死亡的关键调节因子。
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Ferroptosis and Metabolic Dysregulation: Emerging Chemical Targets in Cancer and Infection.铁死亡与代谢失调:癌症和感染中新兴的化学靶点
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Cocrystal structure reveals the mechanism of FSP1 inhibition by FSEN1.共晶结构揭示了FSEN1抑制FSP1的机制。
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Ferroptosis: New Strategies for Clinical Treatment of Rheumatoid Arthritis.铁死亡:类风湿关节炎临床治疗的新策略
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HNRNPC stabilizes m6A-modified AC145207.5 to accelerate tumorigenesis in colorectal cancer by impeding the Nrf2/GPX4 axis-mediated ferroptosis.HNRNPC通过阻碍Nrf2/GPX4轴介导的铁死亡来稳定m6A修饰的AC145207.5,从而加速结直肠癌的肿瘤发生。
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Ferroptosis in Cardiovascular Diseases and Ferroptosis-Related Intervention Approaches.心血管疾病中的铁死亡及铁死亡相关干预方法
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Structural insight into 6-OH-FAD-dependent activation of hFSP1 for ferroptosis suppression.对hFSP1的6-OH-FAD依赖性激活以抑制铁死亡的结构洞察。
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Ketogenic diet reshapes cancer metabolism through lysine β-hydroxybutyrylation.生酮饮食通过赖氨酸β-羟丁酰化重塑癌症代谢。
Nat Metab. 2024 Aug;6(8):1505-1528. doi: 10.1038/s42255-024-01093-w. Epub 2024 Aug 12.
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The Roles of White Adipose Tissue and Liver NADPH in Dietary Restriction-Induced Longevity.白色脂肪组织和肝脏NADPH在饮食限制诱导的长寿中的作用。
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本文引用的文献

1
A non-canonical vitamin K cycle is a potent ferroptosis suppressor.非经典维生素 K 循环是一种有效的铁死亡抑制因子。
Nature. 2022 Aug;608(7924):778-783. doi: 10.1038/s41586-022-05022-3. Epub 2022 Aug 3.
2
Targeting ferroptosis as a vulnerability in cancer.针对癌症中的铁死亡脆弱性。
Nat Rev Cancer. 2022 Jul;22(7):381-396. doi: 10.1038/s41568-022-00459-0. Epub 2022 Mar 25.
3
Ferroptosis: mechanisms, biology and role in disease.铁死亡:机制、生物学及其在疾病中的作用
Nat Rev Mol Cell Biol. 2021 Apr;22(4):266-282. doi: 10.1038/s41580-020-00324-8. Epub 2021 Jan 25.
4
Apoptosis inducing factor and mitochondrial NADH dehydrogenases: redox-controlled gear boxes to switch between mitochondrial biogenesis and cell death.凋亡诱导因子和线粒体 NADH 脱氢酶:氧化还原控制的变速箱,用于在线粒体生物发生和细胞死亡之间切换。
Biol Chem. 2020 Aug 25;402(3):289-297. doi: 10.1515/hsz-2020-0254. Print 2021 Feb 23.
5
MESH1 is a cytosolic NADPH phosphatase that regulates ferroptosis.MESH1是一种调节铁死亡的胞质NADPH磷酸酶。
Nat Metab. 2020 Mar;2(3):270-277. doi: 10.1038/s42255-020-0181-1. Epub 2020 Mar 9.
6
Emerging Mechanisms and Disease Relevance of Ferroptosis.铁死亡的新兴机制及其与疾病的相关性
Trends Cell Biol. 2020 Jun;30(6):478-490. doi: 10.1016/j.tcb.2020.02.009. Epub 2020 Mar 21.
7
Ferroptosis: past, present and future.铁死亡:过去、现在和未来。
Cell Death Dis. 2020 Feb 3;11(2):88. doi: 10.1038/s41419-020-2298-2.
8
The CoQ oxidoreductase FSP1 acts parallel to GPX4 to inhibit ferroptosis.辅酶 Q 氧化还原酶 FSP1 与 GPX4 平行作用以抑制铁死亡。
Nature. 2019 Nov;575(7784):688-692. doi: 10.1038/s41586-019-1705-2. Epub 2019 Oct 21.
9
FSP1 is a glutathione-independent ferroptosis suppressor.FSP1 是一种谷胱甘肽不依赖的铁死亡抑制因子。
Nature. 2019 Nov;575(7784):693-698. doi: 10.1038/s41586-019-1707-0. Epub 2019 Oct 21.
10
Defining NADH-Driven Allostery Regulating Apoptosis-Inducing Factor.定义由NADH驱动的变构调节凋亡诱导因子
Structure. 2016 Dec 6;24(12):2067-2079. doi: 10.1016/j.str.2016.09.012. Epub 2016 Nov 3.

FSP1 oxidizes NADPH to suppress ferroptosis.

作者信息

Zhang Sitao, Gou Shengsong, Zhang Qian, Yong Xin, Gan Boyi, Jia Da

机构信息

Key Laboratory of Birth Defects and Related Diseases of Women and Children, Department of Paediatrics, West China Second University Hospital, State Key Laboratory of Biotherapy, Sichuan University, Chengdu, Sichuan, China.

Department of Experimental Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.

出版信息

Cell Res. 2023 Dec;33(12):967-970. doi: 10.1038/s41422-023-00879-z. Epub 2023 Sep 22.

DOI:10.1038/s41422-023-00879-z
PMID:37739993
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10709417/
Abstract
摘要