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拓展视野:铁死亡在乳腺癌中的多方面作用

Broadening horizons: the multifaceted role of ferroptosis in breast cancer.

作者信息

Ge Anqi, Xiang Wang, Li Yan, Zhao Da, Chen Junpeng, Daga Pawan, Dai Charles C, Yang Kailin, Yan Yexing, Hao Moujia, Zhang Bolin, Xiao Wei

机构信息

The First Hospital of Hunan University of Chinese Medicine, Changsha, Hunan, China.

Department of Rheumatology, The First People's Hospital Changde City, Changde, Hunan, China.

出版信息

Front Immunol. 2024 Nov 27;15:1455741. doi: 10.3389/fimmu.2024.1455741. eCollection 2024.

Abstract

Breast cancer poses a serious threat to women's health globally. Current radiotherapy and chemotherapy regimens can induce drug-resistance effects in cancer tissues, such as anti-apoptosis, anti-pyroptosis, and anti-necroptosis, leading to poor clinical outcomes in the treatment of breast cancer. Ferroptosis is a novel programmed cell death modality characterized by iron overload, excessive generation of reactive oxygen species, and membrane lipid peroxidation. The occurrence of ferroptosis results from the imbalance between intracellular peroxidation mechanisms (executive system) and antioxidant mechanisms (defensive system), specifically involving iron metabolism pathways, amino acid metabolism pathways, and lipid metabolism pathways. In recent years, it has been found that ferroptosis is associated with the progression of various diseases, including tumors, hypertension, diabetes, and Alzheimer's disease. Studies have confirmed that triggering ferroptosis in breast cancer cells can significantly inhibit cancer cell proliferation and invasion, and improve cancer cell sensitivity to radiotherapy and chemotherapy, making induction of ferroptosis a potential strategy for the treatment of breast cancer. This paper reviews the development of the concept of ferroptosis, the mechanisms of ferroptosis (including signaling pathways such as GSH-GPX4, FSP1-CoQ1, DHODH-CoQ10, and GCH1-BH4) in breast cancer disease, the latest research progress, and summarizes the research on ferroptosis in breast cancer disease within the framework of metabolism, reactive oxygen biology, and iron biology. The key regulatory factors and mechanisms of ferroptosis in breast cancer disease, as well as important concepts and significant open questions in the field of ferroptosis and related natural compounds, are introduced. It is hoped that future research will make further breakthroughs in the regulatory mechanisms of ferroptosis and the use of ferroptosis in treating breast cancer cells. Meanwhile, natural compounds may also become a new direction for potential drug development targeting ferroptosis in breast cancer treatment. This provides a theoretical basis and opens up a new pathway for research and the development of drugs for the prevention and treatment of breast cancer.

摘要

乳腺癌在全球范围内对女性健康构成严重威胁。当前的放疗和化疗方案可在癌组织中诱导耐药效应,如抗凋亡、抗焦亡和抗坏死性凋亡,导致乳腺癌治疗的临床效果不佳。铁死亡是一种新型的程序性细胞死亡方式,其特征为铁过载、活性氧过度生成和膜脂质过氧化。铁死亡的发生源于细胞内过氧化机制(执行系统)和抗氧化机制(防御系统)之间的失衡,具体涉及铁代谢途径、氨基酸代谢途径和脂质代谢途径。近年来,人们发现铁死亡与包括肿瘤、高血压、糖尿病和阿尔茨海默病在内的多种疾病的进展有关。研究证实,触发乳腺癌细胞中的铁死亡可显著抑制癌细胞增殖和侵袭,并提高癌细胞对放疗和化疗的敏感性,使诱导铁死亡成为治疗乳腺癌的一种潜在策略。本文综述了铁死亡概念的发展、乳腺癌疾病中铁死亡的机制(包括谷胱甘肽过氧化物酶4、铁死亡抑制蛋白1-辅酶Q1、二氢乳清酸脱氢酶-辅酶Q10和四氢生物蝶呤合成酶-四氢生物蝶呤等信号通路)、最新研究进展,并在代谢、活性氧生物学和铁生物学框架内总结了乳腺癌疾病中铁死亡的研究。介绍了乳腺癌疾病中铁死亡的关键调节因子和机制,以及铁死亡领域的重要概念和重大未解决问题,以及相关天然化合物。希望未来的研究能在铁死亡的调节机制以及铁死亡在治疗乳腺癌细胞中的应用方面取得进一步突破。同时,天然化合物也可能成为乳腺癌治疗中靶向铁死亡的潜在药物开发的新方向。这为乳腺癌的预防和治疗药物的研究与开发提供了理论依据,并开辟了一条新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d11/11631881/010b86ee9234/fimmu-15-1455741-g001.jpg

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