Effectiveness and mode of therapeutic gene delivery in vivo as well as
biological safety of such transfer must be improved before widespread
application of gene therapy in the clinic becomes possible. Most rese
arch has so far focused on recombinant viral delivery systems. Clinica
l future seems to belong, however, to nonviral delivery systems. Such
systems feature DNA complexed to lipid, protein, peptide or polymeric
carriers with ligands allowing in vivo tissue targeting by the complex
and nuclear translocation of the exogene. Nonviral gene carrier syste
ms are discussed together with strategies of destroying cancer cells.