Progesterone and estradiol enhance lipid mediated transfection of Sk-Br-3 mammalian cancer cells.

Frank Köster*, Ricardo Felberbaum, Dominique Finas, Kurt Wünsch, Christiane Schulz, Klaus Diedrich, Charlotte Hauser

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

11 Scopus citations

Abstract

Cyclodextrin encapsulated beta-estradiol and progesterone were used for enhancement of gene delivery using the breast cancer cell line Sk-Br-3. A non-toxic concentration of cyclodextrin encapsulated sex steroids (50 microM) added to lipid or liposomal transfection led to a 12-fold increase of reporter gene expression (luciferase) with progesterone and an 8-fold increase with estradiol using Lipofectamine Plus mediated transfection. Using the lipid formulation Fugene-6 the results were a 5.5-fold and a 4.5-fold increase respectively. This enhancement could only be observed if the sex steroids were added to the cells before application of the DNA-Fugene complex supporting the evidence that intracellular processes are responsible for the activity of the steroids. The strong differences between progesterone and estradiol in modifying Lipofectamine Plus transfection in Sk-Br-3 cells may to be explained by differences in the distribution of these receptors in the cellular compartments. These results seem to add evidence on the possibility of using sex steroids to increase the efficiency of non-viral vectors for transfection, and may ultimately prove to be relevant to gene therapy in the treatment of breast cancer as well as other solid tumors.

Original languageEnglish (US)
Pages (from-to)617-620
Number of pages4
JournalInternational journal of molecular medicine
Volume9
Issue number6
StatePublished - Jan 1 2002

ASJC Scopus subject areas

  • Genetics

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