药物输送
小泡
小干扰RNA
免疫原性
细胞生物学
基因沉默
癌细胞
膜
化学
靶向给药
纳米技术
细胞
生物
癌症研究
癌症
核糖核酸
材料科学
基因
免疫学
生物化学
免疫系统
遗传学
作者
Vipul Gujrati,Sung-Hyun Kim,Sang‐Hyun Kim,Jung Joon Min,Hyon E. Choy,Sun‐Chang Kim,Sangyong Jon
出处
期刊:ACS Nano
[American Chemical Society]
日期:2014-01-10
卷期号:8 (2): 1525-1537
被引量:416
摘要
Advances in genetic engineering tools have contributed to the development of strategies for utilizing biologically derived vesicles as nanomedicines for achieving cell-specific drug delivery. Here, we describe bioengineered bacterial outer membrane vesicles (OMVs) with low immunogenicity that can target and kill cancer cells in a cell-specific manner by delivering small interfering RNA (siRNA) targeting kinesin spindle protein (KSP). A mutant Escherichia coli strain that exhibits reduced endotoxicity toward human cells was engineered to generate OMVs displaying a human epidermal growth factor receptor 2 (HER2)-specific affibody in the membrane as a targeting ligand. Systemic injection of siRNA-packaged OMVs caused targeted gene silencing and induced highly significant tumor growth regression in an animal model. Importantly, the modified OMVs were well tolerated and showed no evidence of nonspecific side effects. We propose that bioengineered OMVs have great potential as cell-specific drug-delivery vehicles for treating various cancers.
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