基因沉默
去唾液酸糖蛋白受体
癌症研究
光热治疗
肝细胞癌
癌细胞
转染
体内
遗传增强
癌症
材料科学
体外
生物
基因
纳米技术
生物化学
肝细胞
生物技术
遗传学
作者
Yanling Liu,Manman Tan,Chunjuan Fang,Xiaoyan Chen,Huan Liu,Ying Feng,Yujuan Zhang,Wei‐Ping Min
出处
期刊:Nanotechnology
[IOP Publishing]
日期:2021-01-14
卷期号:32 (17): 175101-175101
被引量:11
标识
DOI:10.1088/1361-6528/abdbed
摘要
Tumor-specific targeted delivery is a major obstacle to clinical treatment of hepatocellular carcinoma (HCC). Here we have developed a novel multi-functional nanostructure GAL-GNR-siGPC-3, which consists of Galactose (GAL) as the HCC-targeting moiety, golden nanorods (GNR) as a framework to destroy tumor cells under laser irradiation, and siRNA of Glypican-3 (siGPC-3) which induce specifically gene silence of GPC-3 in HCC. Glypican-3 (GPC-3) gene is highly associated with HCC and is a new potential target for HCC therapy. On the other hand, Gal can specifically bind to the asialoglycoprotein receptor which is highly expressed on membrane of hepatoma cells. GAL and siGPC-3 can induce targeted silencing of GPC-3 gene in hepatoma cells. In vivo and in vitro results showed that GAL-GNR-siGPC-3 could significantly induce downregulation of GPC-3 gene and inhibit the progression of HCC. More notably, GAL-GNR-siGPC-3 could induce both GPC-3 gene silencing and photothermal effects, and the synergistic treatment of tumors was more effective than individual treatments. In summary, GAL-GNR-siGPC-3 achieved a synergistic outcome to the treatment of cancer, which opens up a new approach for the development of clinical therapies for HCC.
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