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Journal of International Oncology ; (12): 794-797, 2011.
Article in Chinese | WPRIM | ID: wpr-422195

ABSTRACT

Objective To investigate the G2 cell cycle arrest and apoptosis induced by HIV-1 Vpr gene on Hela,Lovo and HepG2 cancer cells.Methods Recombinant vector pcDNA4-Vpr was constructed by DNA recombination technology and was then transfected into Hela,Lovo and HepG2 cells.Meanwhile,pcDNA4-EGFP plasmid group,FUGENE group and blank group were also set up as control.Ratio of cytostasis was evaluated by MTS assay 24 h,48 h and 72 h later,cell cycle arrest examined by flow cytometry and apoptosis detected by staining with ANNEXIN V and PI double dyes.Results Compared to the control group,the value of inhibition ratio,G2 arrest and apoptosis of Hela,Lovo and HepG2 cells increased obviously 24 h,48 h and 72 h after the transfection ( P < 0.05 ).72 h after the transfection,the inhibition ratio of Hela,Lovo and HepG2 was 29.67%,27.35% and 31.67% respectively.Percentage of G2 phase cells was 24.9%,18.8%and 32.1% respectively.Apoptosis percentage of Hela,Lovo and HepG2 ceils was 15.46%,7.7% and 41.5% correspondingly.Conclusion HIV-1 Vpr gene can induce cell cycle G2 arrest and apoptosis of Hela,Lovo and HepG2 cell lines in vitro.

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