前药
细胞凋亡
程序性细胞死亡
坏死性下垂
阿霉素
癌症研究
癌细胞
化学
药理学
化疗
癌症
生物
生物化学
遗传学
作者
Yong Huang,Yi Lin,Bowen Li,Fu Zhang,Chenyue Zhan,Xin Xie,Zhuo Yao,Chongzhi Wu,Ping Yuan,Jianliang Shen
标识
DOI:10.1016/j.ajps.2023.100844
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.
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