The development of rational and targeted therapies for human astrocytomas i
s heavily dependent on our knowledge of its molecular pathogenesis, combine
d with the generation of appropriate pre-clinical mouse models. The ability
to manipulate the mouse genome, which is nearing completion and is highly
homologous to its human counterpart, has significantly accelerated our abil
ity to create transgenic mouse models that replicate the pathological and m
olecular characteristics found in human astrocytomas. These models should s
erve to further our knowledge of the molecular pathogenesis of human astroc
ytomas, and serve as useful reagents to test conventional and novel thera-b
reak peutics.