肝细胞癌
小干扰RNA
癌基因
癌症研究
转染
免疫印迹
乙型肝炎病毒
体外
遗传增强
病毒学
医学
细胞培养
化学
生物
病毒
癌症
细胞周期
基因
内科学
生物化学
遗传学
作者
Jing Kong,Xiaoping Li,Jianbo Jia,Jinsheng Wu,Ning Wu,Jun Chen,Fang Fang
出处
期刊:Human Gene Therapy Methods
[Mary Ann Liebert]
日期:2015-10-01
卷期号:26 (5): 175-180
被引量:9
标识
DOI:10.1089/hgtb.2015.093
摘要
Hepatocellular carcinoma (HCC) is a deadly human malignant tumor that is among the most common cancers in the world, especially in Asia. Hepatitis B virus (HBV) infection has been well established as a high risk factor for hepatic malignance. Studies have shown that Pokemon is a master oncogene for HCC growth, suggesting it as an ideal therapeutic target. However, efficient delivery system is still lacking for Pokemon targeting treatment. In this study, we used core proteins of HBV, which is modified with RGD peptides, to construct a biomimetic vector for the delivery of Pokemon siRNAs (namely, RGD-HBc-Pokemon siRNA). Quantitative PCR and Western blot assays revealed that RGD-HBc-Pokemon siRNA possessed the highest efficiency of Pokemon suppression in HCC cells. In vitro experiments further indicated that RGD-HBc-Pokemon-siRNA exerted a higher tumor suppressor activity on HCC cell lines, evidenced by reduced proliferation and attenuated invasiveness, than Pokemon-siRNA or RGD-HBc alone. Finally, animal studies demonstrated that RGD-HBc-Pokemon siRNA suppressed the growth of HCC xenografts in mice by a greater extent than Pokemon-siRNA or RGD-HBc alone. Based on the above results, Pokemon siRNA delivery mediated by RGD-modified HBV core protein was shown to be an effective strategy of HCC gene therapy.
科研通智能强力驱动
Strongly Powered by AbleSci AI