We describe here the oncostatin M (OSM)-dependent inhibition of in vivo tum
our formation after intracerebral inoculation of glioblastoma cells in mice
. We generated human glioblastoma cells transfected with the OSM gene under
the control of a tetracycline-response promoter. Upon removal of tetracycl
ine from the medium, cells exhibited a differentiated cell morphology, whil
e proliferation was significantly inhibited. After implantation of these ce
lls into nude mice brains, large tumours developed in animals lacking OSM e
xpression, whereas no tumour formation was observed in mice with induced OS
M expression. Our results suggest that OSM exerts pronounced antitumorigeni
c effects on glioblastoma cells in vivo and provide arguments for a therape
utic application of OSM in humans.