<abstract xml:lang="en" xmlns="http://www.w3.org/1999/xhtml"><bold><italic>Background.</italic></bold> Silencing oncogenes or other genes that contribute to tumor malignancy and progression offers a promising approach to treating cancer. Specific and efficient silencing of gene expression can be achieved by RNA interference (RNAi) technology using small interfering RNA (siRNA) or short hairpin RNA (shRNA). However, a major challenge in RNAi technology is effective delivery of interfering molecules into target cells. The aim of our study was to evaluate electroporation as a perspective method for efficient in vitro transfection of LPB fibrosarcoma cells with plasmid DNA expressing shRNA.<bold><italic>Methods.</italic></bold> Induction of shRNA-mediated gene silencing by electroporation was determined by fluorescence microscopy, flow cytometry and western blot analysis. The effect of electroporation conditions on cell survival and proliferation was determined by clonogenic assay.<bold><italic>Results and conclusions.</italic></bold> Our results demonstrated that electroporation is a feasible and effective method for delivery of plasmid DNA expressing shRNA into cancer cells in vitro. Electrotransfection of murine LPB fibrosarcoma cells, continuously expressing green fluorescence protein - GFP (LPBGFP), with plasmid DNA encoding shRNA-GFP, reduced GFP expression, which was determined on the protein level, as well as by measurement of GFP fluorescence intensity. A pronounced reduction in GFP expression level was detected from the second to the fifth day after treatment. Moreover, the method is easy to perform and showed low cell damaging effects, which are the most important and preferential factors for further in vivo studies.</abstract>

Background. Silencing oncogenes or other genes that contribute to tumor malignancy and progression offers a promising approach to treating cancer. Specific and efficient silencing of gene expression can be achieved by RNA interference (RNAi) technology using small interfering RNA (siRNA) or short hairpin RNA (shRNA). However, a major challenge in RNAi technology is effective delivery of interfering molecules into target cells. The aim of our study was to evaluate electroporation as a perspective method for efficient in vitro transfection of LPB fibrosarcoma cells with plasmid DNA expressing shRNA.Methods. Induction of shRNA-mediated gene silencing by electroporation was determined by fluorescence microscopy, flow cytometry and western blot analysis. The effect of electroporation conditions on cell survival and proliferation was determined by clonogenic assay.Results and conclusions. Our results demonstrated that electroporation is a feasible and effective method for delivery of plasmid DNA expressing shRNA into cancer cells in vitro. Electrotransfection of murine LPB fibrosarcoma cells, continuously expressing green fluorescence protein - GFP (LPBGFP), with plasmid DNA encoding shRNA-GFP, reduced GFP expression, which was determined on the protein level, as well as by measurement of GFP fluorescence intensity. A pronounced reduction in GFP expression level was detected from the second to the fifth day after treatment. Moreover, the method is easy to perform and showed low cell damaging effects, which are the most important and preferential factors for further in vivo studies.

Evaluation of shRNA-mediated gene silencing by electroporation in LPB fibrosarcoma cells

Department of Experimental Oncology, Institute of Oncology, Ljubljana, Slovenia

Radiology and Oncology

Background. Silencing oncogenes or other genes that contribute to tumor malignancy and progression offers a promising approach to treating cancer. Specific and...

Evaluation of shRNA-mediated gene silencing by electroporation in LPB fibrosarcoma cells

Publié en ligne: 11 juin 2008

Pages: 82 - 92

DOI: https://doi.org/10.2478/v10019-008-0007-3

Mots clés
electroporation, plasmid DNA, shRNA, fibrosarcoma

This content is open access.

Evaluation of shRNA-mediated gene silencing by electroporation in LPB fibrosarcoma cells

Publié en ligne: 11 juin 2008

Pages: 82 - 92

DOI: https://doi.org/10.2478/v10019-008-0007-3

Mots cléselectroporation, plasmid DNA, shRNA, fibrosarcoma

This content is open access.

Mots clés
electroporation, plasmid DNA, shRNA, fibrosarcoma