核酸
适体
基因沉默
材料科学
RNA干扰
小干扰RNA
核糖核酸
遗传增强
DNA
基因
癌症研究
细胞生物学
生物
分子生物学
生物化学
作者
Dexuan Xiao,Yanjing Li,Taoran Tian,Tianxu Zhang,Sirong Shi,Boyao Lu,Yang Gao,Xin Qin,Mei Zhang,Wei Wei,Yunfeng Lin
标识
DOI:10.1021/acsami.0c23005
摘要
siRNA is found to effectively knock down the target gene in cells, which is considered a promising strategy for gene therapy. However, the application of siRNA is limited due to its low efficiency of the cellular uptake. Tetrahedral framework nucleic acids (tFNAs) are synthesized by four single-stranded DNAs and show multiple biological functions in recent studies, especially suitable for drug delivery. More than 60% of malignant melanomas are associated with Braf gene mutation, an attractive therapeutic target for RNA interference. In this study, we modified anti-Braf siRNA (siBraf) with tFNAs to downregulate the target gene. Meanwhile, we directly incorporated AS1411 (a DNA aptamer) to our nanostructure, which assists tFNAs to improve the cellular uptake efficacy of siBraf significantly. The results indicated that tFNAs-AS1411-siBraf exhibited more potent activity to cleave Braf mRNA than free siBraf. This study may provide a new idea for the combination therapy of siRNA and aptamers via DNA nanomaterials to achieve gene silencing.
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