体外
化学
体内
细胞凋亡
胶体金
癌症研究
癌细胞
小干扰RNA
转化生长因子
分子生物学
纳米颗粒
癌症
细胞生物学
转染
纳米技术
材料科学
医学
生物
生物化学
内科学
生物技术
基因
作者
Jindao Wu,Bin Liu,Heming Wu,Younong Wu,Wei Zhang,Shouwei Zhao,Long Zhang,Xiongxiong Pan,Wen Gao,Xuehao Wang,Yi Yuan,Yaqin Zhang
标识
DOI:10.1166/jbn.2016.2217
摘要
Nanoparticles, especially gold nanoparticles (AuNPs), have been shown to be an efficient carrier to deliver small RNAs into cancer cells. In this study, we used cysteamine-functionalized AuNPs to effectively deliver TGF-β1 siRNA into hepatoma HepG2 cells in vitro and in vivo. We found that, compared with AuNPs-mediated NC siRNA (AuNP-siNC), AuNPs-delivered TGF-β1 siRNA (AuNP-siTGFβ1) efficiently decreased the level of TGF-β1, increased cell apoptosis, and significantly inhibited the proliferation of recipient tumour cells. Systemic administration of the AuNP-siTGFβ1 complexes into human HepG2 xenografted mice likewise reduced TGF-β1 expression and downstream TGF-β1 signalling. Functionally, AuNP-siTGFβ1 strongly inhibited tumour growth and improved the survival rate of tumour-bearing mice compared with the control groups. In conclusion, our results demonstrate that the siRNA delivery system with AuNP described here appears to be a highly effective method to deliver RNAi therapeutics into tumour cells for oncotherapy.
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