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Construction of adenovirus carrying dual-target shRNA for Oct-4 and Survivin and its inhibitory effect on human hepatocellular carcinoma cells / 生物工程学报
Chinese Journal of Biotechnology ; (12): 623-631, 2012.
Article in Chinese | WPRIM | ID: wpr-342455
ABSTRACT
The transcriptional factor Oct-4 and Survivin are the key regulatory factors in cancer cell proliferation and mitosis. A dual cancer-specific shRNA adenovirus vector, Ad5-Dual-shRNA, targeting Oct-4 and Survivin genes was constructed by molecular cloning and recombination. After cells were infected with virus, hepatocellular carcinoma cell line EHBH-H1 was used for detecting the expression of Oct-4 and Survivin proteins by Western blotting. The viral cytotoxic effect on cancer cells was detected by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) reduction assay in vitro, and the inhibition effect on tumor xenografts was observed in nude mice. The results showed that the expression of Oct-4 and Survivin in cancer cell line EHBH-H1 could be silenced markedly by Ad5-Dual-shRNA. In MTT and animal experiments, Ad5-Dual-shRNA also represented much stronger anti-tumor effect on tumor growth than Ad5-Surv-shRNA and Ad5-Oct4-shRNA. From this research we can draw a conclusion that the cancer-specific adenovirus vector expressing dual-shRNA targeting Oct-4 and Survivin genes may provide us a more effective, specific and convenient gene therapy method.
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Therapeutics / Recombinant Proteins / Transfection / Genetic Therapy / Adenoviridae / Apoptosis / Carcinoma, Hepatocellular / RNA, Small Interfering / Cell Line, Tumor Limits: Animals / Humans Language: Chinese Journal: Chinese Journal of Biotechnology Year: 2012 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Pathology / Therapeutics / Recombinant Proteins / Transfection / Genetic Therapy / Adenoviridae / Apoptosis / Carcinoma, Hepatocellular / RNA, Small Interfering / Cell Line, Tumor Limits: Animals / Humans Language: Chinese Journal: Chinese Journal of Biotechnology Year: 2012 Type: Article