Survivin gene silencing inhibited growth of colon cancer Lovo cells in vitro
Zhong Shi-lon
Abstract
Zhong Shi-lon
Abstract
Objective To investigate the inhibitory effect of surviving-shRNA on survivin gene expression and cell proliferation of the human colon cancer cell.Methods The survivin-shRNA was constructed and transfected into Lovo cells with Lipofectamine.RT-PCR and western blot analysis were used to detect down-regulations of survivin mRNA and protein expressions respectively.Cell proliferation inhibition was determined using MTT assay.Results The expressions of survivin mRNA and protein were successfully suppressed by survivin-shRNA(P0.05),with inhibition rates of 39.59% and 42.32% respectively.MTT assay indicated that the specific shRNA inhibited tumor cell growth in a time-dependent manner since 48 hours post-transfection.The cell viability of surviving-shRNA transfected group decreased significantly to 41.8% at 72 h,which was of statistical significance compared with that of blank control group(P0.05).Conclusion The specific survivin-shRNA could down-regulate the expression of survivin gene and inhibit the growth of Lovo cells in vitro.[
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective To investigate the inhibitory effect of surviving-shRNA on survivin gene expression and cell proliferation of the human colon cancer cell.Methods The survivin-shRNA was constructed and transfected into Lovo cells with Lipofectamine.RT-PCR and western blot analysis were used to detect down-regulations of survivin mRNA and protein expressions respectively.Cell proliferation inhibition was determined using MTT assay.Results The expressions of survivin mRNA and protein were successfully suppressed by survivin-shRNA(P0.05),with inhibition rates of 39.59% and 42.32% respectively.MTT assay indicated that the specific shRNA inhibited tumor cell growth in a time-dependent manner since 48 hours post-transfection.The cell viability of surviving-shRNA transfected group decreased significantly to 41.8% at 72 h,which was of statistical significance compared with that of blank control group(P0.05).Conclusion The specific survivin-shRNA could down-regulate the expression of survivin gene and inhibit the growth of Lovo cells in vitro.[
Key concepts: Survivin, Small hairpin RNA, Transfection, MTT assay, Molecular biology, Cell growth, Lipofectamine, Viability assay