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铁死亡:急性髓系白血病的潜在治疗靶点与预后预测(综述)

Ferroptosis: Potential therapeutic targets and prognostic predictions for acute myeloid leukemia (Review).

作者信息

Zhang Wenlu, Wen Wen, Tan Ran, Zhang Meirui, Zhong Tantan, Wang Jianhong, Chen Haiping, Fang Xiaosheng

机构信息

Department of Hematology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Shandong First Medical University, Jinan, Shandong 250021, P.R. China.

Department of Hematology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong 250021, P.R. China.

出版信息

Oncol Lett. 2024 Sep 30;28(6):574. doi: 10.3892/ol.2024.14707. eCollection 2024 Dec.

DOI:10.3892/ol.2024.14707
PMID:39397802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11467844/
Abstract

Ferroptosis is a relatively recently discovered type of regulated cell death that is induced by iron-dependent lipid peroxidation. The key contributing factors to ferroptosis are the loss of glutathione peroxidase 4 which is required for reversing lipid peroxidation, the buildup of redox-active iron and the oxidation of phospholipids containing polyunsaturated fatty acids. Ferroptosis has been associated with a number of diseases, including cancers such as hepatocellular carcinoma, breast cancer, acute renal damage and neurological disorders such as Alzheimer's disease and Alzheimer's disease, and there may be an association between ferroptosis and acute myeloid leukemia (AML). The present review aims to describe the primary regulatory pathways of ferroptosis, and the relationship between ferroptosis and the occurrence and development of AML. Furthermore, the present review comprehensively summarizes the latest advances in the treatment and prognosis of ferroptosis in AML.

摘要

铁死亡是一种相对较新发现的受调控的细胞死亡类型,由铁依赖性脂质过氧化作用诱导。铁死亡的关键促成因素包括:逆转脂质过氧化作用所需的谷胱甘肽过氧化物酶4的缺失、氧化还原活性铁的积累以及含有多不饱和脂肪酸的磷脂的氧化。铁死亡与多种疾病相关,包括肝细胞癌、乳腺癌等癌症、急性肾损伤以及阿尔茨海默病等神经疾病,并且铁死亡与急性髓系白血病(AML)之间可能存在关联。本综述旨在描述铁死亡的主要调控途径,以及铁死亡与AML发生发展之间的关系。此外,本综述全面总结了AML中铁死亡治疗和预后的最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc2f/11467844/f9a79c9f106c/ol-28-06-14707-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc2f/11467844/f9a79c9f106c/ol-28-06-14707-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc2f/11467844/f9a79c9f106c/ol-28-06-14707-g00.jpg

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本文引用的文献

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Emerging role of glutathione peroxidase 4 in myeloid cell lineage development and acute myeloid leukemia.谷胱甘肽过氧化物酶 4 在髓系细胞谱系发育和急性髓系白血病中的新作用。
Cell Mol Biol Lett. 2024 Jul 8;29(1):98. doi: 10.1186/s11658-024-00613-6.
2
The sensitivity of acute myeloid leukemia cells to cytarabine is increased by suppressing the expression of Heme oxygenase-1 and hypoxia-inducible factor 1-alpha.通过抑制血红素加氧酶-1和缺氧诱导因子1-α的表达,可增加急性髓系白血病细胞对阿糖胞苷的敏感性。
Cancer Cell Int. 2024 Jun 25;24(1):217. doi: 10.1186/s12935-024-03393-3.
3
Effects of ferroptosis-related gene HSPB1 on acute myeloid leukemia.
铁死亡相关基因 HSPB1 对急性髓系白血病的影响。
Int J Lab Hematol. 2024 Oct;46(5):899-909. doi: 10.1111/ijlh.14319. Epub 2024 Jun 2.
4
Author Correction: Apolipoprotein C1 promotes glioblastoma tumorigenesis by reducing KEAP1/NRF2 and CBS-regulated ferroptosis.作者更正:载脂蛋白C1通过降低KEAP1/NRF2和CBS调节的铁死亡促进胶质母细胞瘤的肿瘤发生。
Acta Pharmacol Sin. 2024 Oct;45(10):2226-2227. doi: 10.1038/s41401-024-01271-2.
5
Ferroptotic therapy in cancer: benefits, side effects, and risks.铁死亡疗法在癌症中的应用:获益、副作用和风险。
Mol Cancer. 2024 May 3;23(1):89. doi: 10.1186/s12943-024-01999-9.
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Correction: Mitochondrial regulation of GPX4 inhibition-mediated ferroptosis in acute myeloid leukemia.更正:急性髓系白血病中GPX4抑制介导的铁死亡的线粒体调控
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