Combination therapy to overcome ferroptosis resistance by biomimetic self-assembly nano-prodrug

被引:6
|
作者
Huang, Yong [2 ,3 ,4 ]
Lin, Yi [1 ,5 ]
Li, Bowen [2 ]
Zhang, Fu [2 ]
Zhan, Chenyue [2 ]
Xie, Xin [3 ,4 ]
Yao, Zhuo [2 ]
Wu, Chongzhi [2 ]
Ping, Yuan [2 ]
Shen, Jianliang [1 ,5 ]
机构
[1] Wenzhou Med Univ, Sch Ophthalmol & Optometry, Sch Biomed Engn, Wenzhou 325035, Peoples R China
[2] Zhejiang Univ, Coll Pharmaceut Sci, Hangzhou 310058, Peoples R China
[3] Guangdong Med Univ, Guangdong Prov Key Lab Res & Dev Nat Drugs, Dongguan 523808, Peoples R China
[4] Guangdong Med Univ, Sch Pharm, Dev Nat Drugs, Dongguan 523808, Peoples R China
[5] Univ Chinese Acad Sci, Wenzhou Inst, Wenzhou 325000, Peoples R China
基金
中国国家自然科学基金;
关键词
Self-assembly nano-prodrug; Ferroptosis; Apoptosis; Combination therapy;
D O I
10.1016/j.ajps.2023.100844
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ferroptosis has emerged as a potent form of no-apoptotic cell death that offers a promising alternative to avoid the chemoresistance of apoptotic pathways and serves as a vulnerability of cancer. Herein, we have constructed a biomimetic self-assembly nano-prodrug system that enables the co-delivery of gefitinib (Gefi), ferrocene (Fc) and dihydroartemisinin (DHA) for the combined therapy of both ferroptosis and apoptosis. In the tumor microenvironment, this nano-prodrug is able to disassemble and trigger drug release under high levels of GSH. Interestingly, the released DHA can downregulate GPX4 level for the enhancement of intracellular ferroptosis from Fc, further executing tumor cell death with concomitant chemotherapy by Gefi. More importantly, this nano-prodrug provides highly homologous targeting ability by coating related cell membranes and exhibits outstanding inhibition of tumor growth and metastasis, as well as no noticeable side-effects during treatments. This simple small molecular self-assembled nano-prodrug provides a new reasonably designed modality for ferroptosis-combined chemotherapy. (c) 2023 Shenyang Pharmaceutical University. Published by Elsevier B.V. ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )
引用
收藏
页数:13
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