Human survivin targeted siRNA enhances osteosarcoma cell SOSP-9607 apoptosis
Zhen-gang Ji
Abstract
Zhen-gang Ji
Abstract
Objective:To explore the effect of siRNA on the expression of survivin in gene and leading apoptosis in osteosarcoma cell line SOSP-9607 using siRNA eukaryotic expression vector.Methods:According to survivin cDNA coding sequence,the specific RNA interference(RNAi) fragments targeting survivin gene were designed and synthesized,which were cloned into pSilencer 3.0-H1 neoplasmid vector,and the siRNA eukaryotic expression vector siRNA survivin targeting survivin gene was constructed.After the vector was constructed,SOSP-9607 cells were transfected with negative control vector or RNAi vectors and selected by G418.Expression of protein of surviving in the stable transfected cells was investigated by Western blot.The above cells were cultured,thus growth curve was drawn.These cells cultured on cover slips were observed through electronmicroscopy.Apoptosis analysis was finished by AnnexinⅤand Hoechst staining.Results:The specific siRNA eukaryotic expression vector PS targeting survivin gene were constructed successfully.The stable transfectants containing negative control vector and PS were obtained.Expression of protein of survivin was inhibited significantly in SOSP-9607/PS cells,whereas survivin gene expression levels were hardly changed in other groups.Otherwise,apoptosic rate was increased significantly in SOSP-9607/PS cells than other two group(P0.01).Conclusion:survivin gene expression can be suppressed markedly by specific siRNA which induced apoptosis in SOSP-9607 cells,the current results establish the experimental foundation for further studying the biological functions and its mechanisms of survivin in SOSP-9607 cells.
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Objective:To explore the effect of siRNA on the expression of survivin in gene and leading apoptosis in osteosarcoma cell line SOSP-9607 using siRNA eukaryotic expression vector.Methods:According to survivin cDNA coding sequence,the specific RNA interference(RNAi) fragments targeting survivin gene were designed and synthesized,which were cloned into pSilencer 3.0-H1 neoplasmid vector,and the siRNA eukaryotic expression vector siRNA survivin targeting survivin gene was constructed.After the vector was constructed,SOSP-9607 cells were transfected with negative control vector or RNAi vectors and selected by G418.Expression of protein of surviving in the stable transfected cells was investigated by Western blot.The above cells were cultured,thus growth curve was drawn.These cells cultured on cover slips were observed through electronmicroscopy.Apoptosis analysis was finished by AnnexinⅤand Hoechst staining.Results:The specific siRNA eukaryotic expression vector PS targeting survivin gene were constructed successfully.The stable transfectants containing negative control vector and PS were obtained.Expression of protein of survivin was inhibited significantly in SOSP-9607/PS cells,whereas survivin gene expression levels were hardly changed in other groups.Otherwise,apoptosic rate was increased significantly in SOSP-9607/PS cells than other two group(P0.01).Conclusion:survivin gene expression can be suppressed markedly by specific siRNA which induced apoptosis in SOSP-9607 cells,the current results establish the experimental foundation for further studying the biological functions and its mechanisms of survivin in SOSP-9607 cells.
Key concepts: Survivin, Transfection, Molecular biology, RNA interference, Gene, Apoptosis, Expression vector, Small interfering RNA