5′-Triphosphate-siRNA Against Survivin Gene Induces Interferon Production and Inhibits Proliferation of Lung Cancer Cells In Vitro

生存素 小干扰RNA 癌症研究 基因沉默 RNA干扰 转染 细胞凋亡 化学 肺癌 下调和上调 癌细胞 A549电池 癌症 生物 医学 基因 核糖核酸 肿瘤科 内科学 生物化学
作者
Kai Wang,Xiaojuan Chen,Fei Yan,Yaling Xing,Xingxing Yang,Jian Tu,Zhongbin Chen
出处
期刊:Journal of Immunotherapy [Lippincott Williams & Wilkins]
卷期号:36 (5): 294-304 被引量:16
标识
DOI:10.1097/cji.0b013e318294183b
摘要

Survivin is a new member of the inhibitors of apoptosis family and upregulated in various human malignancies including human lung cancer. In this study, we proposed a new strategy for RNA interference (RNAi)-mediated anticancer therapy combining activation of interferon production with RNAi using 5'-triphosphate-siRNA (3p-siRNA) against survivin gene. We designed and generated 3p-siRNA targeting human survivin gene (3p-survivin-siRNA). The findings reported here demonstrated that 3p-survivin-siRNA induced a 3p-dependent type-I interferon response when transfected into human lung cancer cells. The 3p-survivin-siRNA significantly inhibited lung cancer cell proliferation in a 3p-dependent manner. The anticancer effect of 3p-survivin-siRNA was superior to that of conventional siRNA. The expression level of survivin in 3p-survivin-siRNA-treated A549 cells was significantly lower than that of siRNA. Furthermore, when 3p-survivin-siRNA silencing approach was combined with radiation treatment, 3p-survivin-siRNA increases the cytotoxicity of A549 cells and induces more cells to undergo apoptosis. In conclusion, our results suggest that 3p-survivin-siRNA could act as a powerful bifunctional molecule with potential for developing promising radiosensitization therapeutics against human lung cancer.
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