With the advent of transgenic technology, novel animal models are being dev
eloped to facilitate prostate cancer research. The ability to perform genet
ic perturbation studies in a temporally and spatially restricted manner has
established a new paradigm for investigations of the molecular mechanisms
involved in the initiation, progression and metastogenesis of prostate canc
er. Using the transgenic adenocarcinoma of the mouse prostate (TRAMP) model
we have begun to identify specific molecular events related to the emergen
ce of the androgen-insensitive phenotype. In addition, a number of new mode
ls have recently been generated to characterize how the deregulation of str
omal to epithelial interactions mediated by polypeptide growth factor signa
ling could facilitate transformation of the prostate. It is anticipated tha
t these models and their successors will ultimately provide new molecular p
athway-based strategies for the prevention, detection and treatment of pros
tate cancer.