Gene therapy strategies for cancer currently aim at targeting gene delivery
to the malignant cell, In a mouse model of intracerebral Lewis lung carcin
oma (3LL), adenoviral vectors transduce not only 3LL cells but also brain p
arenchymal cells including endothelial cells, neurons, microglia, and astro
cytes similar to in vivo similar to. Furthermore, transgene expression pers
ists longer in brain than in tumor. Transfer of IFN-gamma into brain parenc
hymal tells rather than tumor is both necessary and sufficient to generate
antitumor therapeutic benefits. Therefore, parenchymal cells represent an e
ffective and necessary target for delivery of genes that render the brain u
ninhabitable by the tumor.