FEBS Letters · 1996 · 426 citations · 14 references
Life SciencesBiotechnologyMolecular BiologyGene DeliveryGene ExpressionGene TherapyGene Delivery SystemsGene Delivery VectorsIn Vivo Gene DeliveryIn Vivo Gene TherapyElectroporationElectroporation-mediated DeliveryGene ElectrotransferMarker Gene ExpressionNonviral Gene Delivery VectorsNonviral VectorsTransfection Efficiencyβ-Galactosidase Reporters
In vivo targeted gene transfer by non-viral vectors is subjected to anatomical constraints depending on the route of administration. Transfection efficiency and gene expression in vivo using non-viral vectors is also relatively low. We report that in vivo electropermeabilization of the liver tissue of rats in the presence of genes encoding luciferase or beta-galactosidase resulted in the strong expression of these genetic markers in rat liver cells. About 30-40% of the rat liver cells electroporated expressed the beta-galactosidase genetic marker 48 h after electroporation. The marker expression was also detected at least 21 days after transfection at about 5% of the level 48 h after electroporation. The results indicate that gene transfer by electroporation in vivo may avoid anatomical constraints and low transfection efficiency.
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Gene transfer into mouse lyoma cells by electroporation in high electric fields.
E. Neumann, Maria Schaefer-Ridder, Y. Wang et al. · The EMBO Journal · 1982 · 2.5K citations · Full text
Drug sensitivity ("suicide") genes for selective cancer chemotherapy.
Moolten Fl · PubMed · 1994 · 275 citations
Medicine, Oncology, Pharmacology +9