Silencing survivin gene inhibits cell proliferation and hTERT expression in SW480 cells
Wang Pin
Abstract
Wang Pin
Abstract
Objective Observation of survivin gene interference effect on the proliferation of SW480 cells,to investigate the effects of the gene expression of hTERT and its mechanism of interference. Methods Small hairpin RNA targeting survivin was synthesized and recombinant plasmid pGenesil-1. 1-survivin was constructed. The siRNA recombinant was transfected into SW480 cell lines. Cell proliferation activity was detected by MTT and the cell cycles were analyzed by flow cytometry. The expression of hTERT,Sp1 mRNA and protein were analyzed by The real-time fluorescence quantitative PCR and western blot. Telomerase activity was examined by TRAP-ELISA analysis. To construct the interference vector targeting Sp1 and transfect into SW480 cell,hTERT mRNA and protein,telomerase activity were examined. Results The cell proliferation rate of SW480 cells transfected with siRNA-survivin recombinant vector was significantly decreased,the inhibitory rate of cell proliferation was 34. 44%( P 0. 05),an increase in the percentage of cells in the G0/G1 phase and a decrease in the percentage of cells in the S and G2/M phase ( P 0. 01). that expression of hTERT and Sp1 mRNA and protein,telomerase activity decreased in shRNA-survivin and shRNA-Sp1 transfected cells( P 0. 01). Conclusions Silencing survivin gene significantly inhibited the proliferation of SW480 cells and down-regulatied hTERT gene expression,its mechanism may be related with down-regulaed Sp1 gene expression.
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Objective Observation of survivin gene interference effect on the proliferation of SW480 cells,to investigate the effects of the gene expression of hTERT and its mechanism of interference. Methods Small hairpin RNA targeting survivin was synthesized and recombinant plasmid pGenesil-1. 1-survivin was constructed. The siRNA recombinant was transfected into SW480 cell lines. Cell proliferation activity was detected by MTT and the cell cycles were analyzed by flow cytometry. The expression of hTERT,Sp1 mRNA and protein were analyzed by The real-time fluorescence quantitative PCR and western blot. Telomerase activity was examined by TRAP-ELISA analysis. To construct the interference vector targeting Sp1 and transfect into SW480 cell,hTERT mRNA and protein,telomerase activity were examined. Results The cell proliferation rate of SW480 cells transfected with siRNA-survivin recombinant vector was significantly decreased,the inhibitory rate of cell proliferation was 34. 44%( P 0. 05),an increase in the percentage of cells in the G0/G1 phase and a decrease in the percentage of cells in the S and G2/M phase ( P 0. 01). that expression of hTERT and Sp1 mRNA and protein,telomerase activity decreased in shRNA-survivin and shRNA-Sp1 transfected cells( P 0. 01). Conclusions Silencing survivin gene significantly inhibited the proliferation of SW480 cells and down-regulatied hTERT gene expression,its mechanism may be related with down-regulaed Sp1 gene expression.
Key concepts: Survivin, Telomerase reverse transcriptase, Molecular biology, Transfection, Small hairpin RNA, Gene silencing, RNA interference, Cell growth