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铁死亡在癌症与药物研发中的最新进展

Recent progress of ferroptosis in cancers and drug discovery.

作者信息

Wang Xiang, Ren Xinxin, Lin Xu, Li Qi, Zhang Yingqiong, Deng Jun, Chen Binxin, Ru Guoqing, Luo Ying, Lin Nengming

机构信息

Department of Pharmacy, Key Laboratory of Clinical Cancer Pharmacology and Toxicology Research of Zhejiang Province, Affiliated Hangzhou First People's Hospital, School of Medicine, Westlake University, Hangzhou 310006, China.

Department of Pathology, Zhejiang Provincial People's Hospital (Affiliated People's Hospital, Hangzhou Medical College), Hangzhou 310014, China.

出版信息

Asian J Pharm Sci. 2024 Aug;19(4):100939. doi: 10.1016/j.ajps.2024.100939. Epub 2024 Jun 26.

DOI:10.1016/j.ajps.2024.100939
PMID:39246507
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11378902/
Abstract

Ferroptosis is a nonapoptotic form of cell death characterized by iron dependence and lipid peroxidation. Ferroptosis is involved in a range of pathological processes, such as cancer. Many studies have confirmed that ferroptosis plays an essential role in inhibiting cancer cell proliferation. In addition, a series of small-molecule compounds have been developed, including erastin, RSL3, and FIN56, which can be used as ferroptosis inducers. The combination of ferroptosis inducers with anticancer drugs can produce a significant synergistic effect in cancer treatment, and patients treated with these combinations exhibit a better prognosis than patients receiving traditional therapy. Therefore, a thorough understanding of the roles of ferroptosis in cancer is of great significance for the treatment of cancer. This review mainly elaborates the molecular biological characteristics and mechanism of ferroptosis, summarizes the function of ferroptosis in cancer development and treatment,illustrates the application of ferroptosis in patient's prognosis prediction and drug discovery, and discusses the prospects of targeting ferroptosis.

摘要

铁死亡是一种非凋亡形式的细胞死亡,其特征为铁依赖性和脂质过氧化。铁死亡参与了一系列病理过程,如癌症。许多研究证实,铁死亡在抑制癌细胞增殖中起重要作用。此外,已经开发出一系列小分子化合物,包括埃拉斯汀、RSL3和FIN56,它们可用作铁死亡诱导剂。铁死亡诱导剂与抗癌药物联合使用可在癌症治疗中产生显著的协同效应,接受这些联合治疗的患者比接受传统治疗的患者预后更好。因此,深入了解铁死亡在癌症中的作用对癌症治疗具有重要意义。本文综述主要阐述了铁死亡的分子生物学特征和机制,总结了铁死亡在癌症发生发展和治疗中的作用,阐述了铁死亡在患者预后预测和药物发现中的应用,并探讨了靶向铁死亡的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0514/11378902/a7333d2c3917/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0514/11378902/eb49a3b04654/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0514/11378902/2d412d65e557/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0514/11378902/eae7a13a4110/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0514/11378902/a7333d2c3917/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0514/11378902/eb49a3b04654/ga1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0514/11378902/2d412d65e557/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0514/11378902/eae7a13a4110/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0514/11378902/a7333d2c3917/gr3.jpg

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本文引用的文献

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The cell biology of ferroptosis.铁死亡的细胞生物学。
Nat Rev Mol Cell Biol. 2024 Jun;25(6):424-442. doi: 10.1038/s41580-024-00703-5. Epub 2024 Feb 16.
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Luteolin induces ferroptosis in prostate cancer cells by promoting TFEB nuclear translocation and increasing ferritinophagy.木犀草素通过促进转录因子EB(TFEB)核转位和增加铁自噬来诱导前列腺癌细胞发生铁死亡。
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SLC38A5 Modulates Ferroptosis to Overcome Gemcitabine Resistance in Pancreatic Cancer.SLC38A5 调节铁死亡以克服胰腺癌对吉西他滨的耐药性。
环状RNA ASH1L通过吸附miR-515-5p调控卵巢癌细胞中细胞周期相关蛋白CDCA7/RRM2,从而抑制铁死亡并增强顺铂耐药性。
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Optimizing chemotherapeutic targets in non-small cell lung cancer with transfer learning for precision medicine.利用迁移学习优化非小细胞肺癌化疗靶点以实现精准医疗。
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Cold atmospheric plasma drives USP49/HDAC3 axis mediated ferroptosis as a novel therapeutic strategy in endometrial cancer via reinforcing lactylation dependent p53 expression.冷大气等离子体通过增强乳酸化依赖性p53表达,驱动USP49/HDAC3轴介导的铁死亡,作为子宫内膜癌的一种新型治疗策略。
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