Development of transferrin-polycation/DNA based vectors for gene delivery to melanoma cells

We describe the comparison of non-viral polycation transfection reagents, a denovirus-enhanced transferrinfection (AVET), polyethylenimine (PEI800) and transferrin conjugated PEI800 (Tf-PEI800) in their ability to transfect mu rine and primary human melanoma cell lines. Expression of a reporter gene, cell surface marker and secreted protein (interleukin-2) was assessed for e ach vector system. Testing for luciferase reporter gene expression in murin e and primary human cell lines, AVET and Tf-PEI800, both showed high levels of expression and comparable activity. Furthermore, when the melanoma cell line B16F10 was transfected with a cell surface marker up to similar to 97 % of the cells expressed the protein on the cell surface. Assessing the lev els of secreted IL-2 in murine cell lines, AVET/IL-2, Tf-PEI800/IL-2 and PE I800/IL-2 all expressed high levels of the cytokine (up to 20 mu g IL-2/10( 6) cells/24 h). In primary human melanoma cell lines, AVET/IL-2 transfected cells secreted more IL-2 than cells transfected with either Tf-PEI800/IL-2 or PEI800/IL-2. In murine melanoma cell culture experiments, positively ch arged PEI800/ DNA and Tf-PEI800/DNA complexes gave similar transfection eff iciencies. However, when subcutaneous tumors in mice were injected with the luciferase reporter gene complexed with either Tf-PEI800 or AVET, higher t ransfection activity was measured in the tumors as compared to ligand free PEI800/DNA complexes.