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癌症治疗中的铁死亡:通往罗马的另一条路。

Ferroptosis in Cancer Treatment: Another Way to Rome.

作者信息

Wu Yinan, Yu Chengcheng, Luo Meng, Cen Chen, Qiu Jili, Zhang Suzhan, Hu Kaimin

机构信息

Department of Breast Surgery, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.

The Key Laboratory of Cancer Prevention and Intervention, China National Ministry of Education, Zhejiang University School of Medicine, Hangzhou, China.

出版信息

Front Oncol. 2020 Sep 25;10:571127. doi: 10.3389/fonc.2020.571127. eCollection 2020.

DOI:10.3389/fonc.2020.571127
PMID:33102227
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7546896/
Abstract

Ferroptosis is a newly described type of programmed cell death and intensively related to both maintaining homeostasis and the development of diseases, especially cancers. Inducing ferroptosis leads to mitochondrial dysfunction and toxic lipid peroxidation in cells, which plays a pivotal role in suppressing cancer growth and progression. Here, we reviewed the existing studies about the molecular mechanisms of ferroptosis involved in different antitumor treatments, such as chemotherapy, targeted therapy, radiotherapy, and immunotherapy. We focused in particular on the distinct combinatorial therapeutic effects such as the synergistic sensitization effect and the drug-resistance reversal achieved when using ferroptosis inducers with conventional cancer therapy. Finally, we discussed the challenges and opportunities in clinical applications of ferroptosis. The application of nanotechnolgy and other novel technologies may provide a new direction in ferroptosis-driven cancer therapies.

摘要

铁死亡是一种新描述的程序性细胞死亡类型,与维持体内平衡和疾病尤其是癌症的发展密切相关。诱导铁死亡会导致细胞内线粒体功能障碍和有毒脂质过氧化,这在抑制癌症生长和进展中起关键作用。在此,我们综述了现有关于铁死亡分子机制的研究,这些机制涉及不同的抗肿瘤治疗,如化疗、靶向治疗、放疗和免疫治疗。我们特别关注了独特的联合治疗效果,例如使用铁死亡诱导剂与传统癌症治疗时所实现的协同增敏作用和耐药逆转。最后,我们讨论了铁死亡临床应用中的挑战与机遇。纳米技术和其他新技术的应用可能为铁死亡驱动的癌症治疗提供新方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0b9/7546896/e2e9fe3afd2d/fonc-10-571127-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0b9/7546896/066226797033/fonc-10-571127-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0b9/7546896/e8de614e1f9a/fonc-10-571127-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0b9/7546896/e2e9fe3afd2d/fonc-10-571127-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0b9/7546896/066226797033/fonc-10-571127-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0b9/7546896/e8de614e1f9a/fonc-10-571127-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0b9/7546896/e2e9fe3afd2d/fonc-10-571127-g0003.jpg

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本文引用的文献

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Cysteine depletion induces pancreatic tumor ferroptosis in mice.半胱氨酸耗竭诱导小鼠胰腺肿瘤发生铁死亡。
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Irradiated tumor cell-derived microparticles mediate tumor eradication via cell killing and immune reprogramming.辐照肿瘤细胞衍生的微粒通过细胞杀伤和免疫重编程来介导肿瘤清除。
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CD44 variant exons induce chemoresistance by modulating cell death pathways.CD44可变外显子通过调节细胞死亡途径诱导化学抗性。
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Molecular mechanism of ZC3H13 -mediated ferroptosis in doxorubicin resistance of triple negative breast cancer.ZC3H13介导的铁死亡在三阴性乳腺癌多柔比星耐药中的分子机制
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A novel defined risk signature of ferroptosis-related lncRNAs for predicting prognosis, immune infiltration, and chemotherapy response in multiple myeloma.一种用于预测多发性骨髓瘤预后、免疫浸润和化疗反应的新型铁死亡相关lncRNA定义风险特征。
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GTP Cyclohydrolase 1/Tetrahydrobiopterin Counteract Ferroptosis through Lipid Remodeling.鸟苷三磷酸环化水解酶1/四氢生物蝶呤通过脂质重塑对抗铁死亡。
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