盐霉素
癌症干细胞
癌细胞
细胞凋亡
癌症研究
下调和上调
干细胞
脂质体
癌症
生物
化学
细胞生物学
生物化学
遗传学
基因
抗生素
作者
Shiyang Shen,Shiqi Lin,Yuying Chen,Ying Zhang,Yingjiao He,Xiao Xu,Yang Feng,Yougong Lu,Ran Mo
出处
期刊:Nano Letters
[American Chemical Society]
日期:2022-03-07
卷期号:22 (6): 2419-2428
被引量:18
标识
DOI:10.1021/acs.nanolett.2c00004
摘要
Antibody-based therapeutics, which induce apoptosis of malignant cells by selectively binding to their receptors, hold tremendous promise for clinical cancer therapy. Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) has received considerable interest due to its favorable capability of activating apoptosis in cancer cells by interacting with death receptors (DRs). However, cancer stem-like cells (CSCs) show deficient or lower DR and are highly resistant to TRAIL-mediated apoptosis limiting the therapeutic efficacy. Here, we report a liposome-mediated acclimatization strategy to overcome the CSC-emanated TRAIL resistance. The liposomal assemblies coencapsulating plasmid DNA encoding TRAIL and salinomycin enable cancer cells as protein generators to express TRAIL, and more importantly, can acclimatize resistant CSCs to be sensitized to the TRAIL-triggered apoptosis by salinomycin-induced upregulation of DR expression on CSCs. This programmable liposome-based drug codelivery system shows the potential to efficiently eliminate CSCs and inhibit CSC-enriched tumor growth in the orthotopic colon tumor mouse model.
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