Antitumor effects of Apoptin gene against hepatoma cells in vivo and in vitro
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Abstract:
Objective:To investigate the antitumor effects of Apoptin against human hepatocellular carcinoma HepG2 cells and implanted H22 tumors in C57BL/6 mice. Methods: C57BL/6 mice were used to establish H22bearing models. pVAX1Apoptin was intratumorally injected and the inhibition of tumor growth was observed. Recombinant plasmid pVAX1Apoptin was transfected into HepG2 cells by Lipofectamine. The expression of Apoptin protein in HepG2 cells was examined by Western blotting. Antitumor effect of pVAX1Apoptin on HepG2 cells was measured by MTT assay, and the apoptosis of HepG2 cells after transfected with pVAX1Apoptin was observed by AO/EB staining.Results:Apoptin gene was effectively expressed in HepG2 cells after transfection with pVAX1Apoptin. pVAX1Apoptin induced apoptosis of HepG2 cells and inhibited the growth of HepG2 cells, with the suppression rate being 69.28% at 48 h after transfection. Intratumoral injection of pVAX1Apoptin significantly inhibited tumor growth, with tumor inhibition rate being 46.71% and mice survival rate being 40% at 39 d after injection. Conclusion: pVAX1Apoptin can inhibit the proliferation of HepG2 cells, and intratumoral injection of pVAX1Apoptin can greatly inhibit tumor growth in vivo.
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Supported by the National High Techology Research and Development Program (863) of China (No. 2007AA021004)