Much of the advancement in mouse models for cancer during the past 2 decade
s can be attributed to our increasing capacity to specifically modify the m
ouse germ line. The first generations of oncomice and tumor-suppressor gene
knockouts are now being succeeded by regulatable or conditional mouse tumo
r models, which can be utilized more effectively to establish correlations
between distinct genetic lesions and specific tumor characteristics and to
design and improve therapeutic intervention strategies. In this review we t
ry to ave the reader a flavor of how the latest reagents can be utilized. (
C) 2001 Academic Press.