Background: The ''Adeno-Virus-Enhanced-Receptor-Mediated'' (AVET)-Syst
em uses the receptor-mediated endocytosis route to introduce DNA into
mammalian cells. By the help of a replication defective adenovirus wit
h endosomolytic activity the coentry of receptor-bound DNA particles i
s faciliated. The transport to the nucleus followed by gene expression
is multifold enhanced. Methods: Two different permanent cell lines fr
om head and neck squamous cell cancer were transfected with the report
ergene for luciferase with either AVET or different liposoms in vitro.
Results: In comparison it becomes obvious, that AVET shows a multifol
d higher transfection rate in vitro than the liposomal formulations ap
plied. Conclusions: AVET could be used for efficient transfection of e
pithelial cells, that are fairly reluctant to DNA transfer. Further tr
ials in the mouse model must prove a possible application in vivo.