纳米载体
RNA干扰
小发夹RNA
多重耐药
阿霉素
生存素
癌症研究
P-糖蛋白
遗传增强
抗药性
DNA
生物
化学
基因
核糖核酸
药理学
化疗
药品
生物化学
遗传学
作者
Jianbing Liu,Linlin Song,Shaoli Liu,Shuai Zhao,Qiao Jiang,Baoquan Ding
标识
DOI:10.1002/anie.201809452
摘要
Abstract Multidrug resistance (MDR) is a major obstacle in the clinical treatment of cancer. Herein, a facile strategy is reported to construct a versatile DNA nanostructure as a co‐delivery vector of RNA interference (RNAi) and chemodrugs to combat multidrug‐resistant tumor (MCF‐7R) in vitro and in vivo. In the tailored nanocarrier, two linear small hairpin RNA (shRNA) transcription templates targeting MDR‐associated genes (gene of P‐glycoprotein, a typical drug efflux pump; and gene of survivin, a representative anti‐apoptotic protein) are precisely organized in the chemodrug (doxorubicin, DOX) pre‐loaded DNA origami. With the incorporation of active targeting and controlled‐release elements, these multifunctional DNA nanocarriers can successfully enter the target MCF‐7R cells and synergistically inhibit tumor growth without apparent systemic toxicity. This tailored DNA nanoplatform, which combines RNAi therapy and chemotherapy, provides a new strategy for the treatment of multidrug‐resistant tumors.
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