Mechanisms and therapeutic targets of ferroptosis: Implications for nanomedicine design

被引:2
|
作者
Zhang, Meihong [1 ]
Guo, Mengqin [1 ]
Gao, Yue [1 ]
Wu, Chuanbin [1 ]
Pan, Xin [2 ]
Huang, Zhengwei [1 ]
机构
[1] Univ Jinan, Coll Pharm, Guangzhou 510632, Peoples R China
[2] Univ Sun Yat Sen, Coll Pharm, Guangzhou 510275, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Ferroptosis; Mechanisms; Therapeutic targets; Nanomedicines; CELL-DEATH; CANCER-CELLS; EMERGING MECHANISMS; IRON; INHIBITION; INSIGHTS; DISEASES; GPX4; FSP1;
D O I
10.1016/j.jpha.2024.03.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ferroptosis is a nonapoptotic form of cell death and differs considerably from the well-known forms of cell death in terms of cell morphology, genetics, and biochemistry. The three primary pathways for cell ferroptosis are system Xc /glutathione peroxidase 4 (GPX4), lipid metabolism, and ferric metabolism. Since the discovery of ferroptosis, mounting evidence has revealed its critical regulatory role in several diseases, especially as a novel potential target for cancer therapy, thereby attracting increasing attention in the fields of tumor biology and anti-tumor therapy. Accordingly, broad prospects exist for identifying ferroptosis as a potential therapeutic target. In this review, we aimed to systematically summarize the activation and defense mechanisms of ferroptosis, highlight the therapeutic targets, and discuss the design of nanomedicines for ferroptosis regulation. In addition, we opted to present the advantages and disadvantages of current ferroptosis research and provide an optimistic vision of future directions in related fields. Overall, we aim to provide new ideas for further ferroptosis research and inspire new strategies for disease diagnosis and treatment. (c) 2024 The Authors. Published by Elsevier B.V. on behalf of Xi'an Jiaotong University. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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页数:17
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