Objectives: Reliable and adequate animal models are required, not only
for investigation of etiology, pathogenesis, and treatment of prostat
e cancer, but also for chemoprevention of prostatic carcinogenesis. Me
thods: Animal models for the study of premalignant changes in the pros
tate are reviewed in the paper, with specific reference to the neonata
lly estrogenized mouse model. Results: Neonatal treatment of newborn H
an:NMRI mice with synthetic nonsteroidal estrogen, diethylstilbestrol
(DES; 2 mu g/pup on days 1-3 after birth) promoted hyperplastic and dy
splastic changes in the periurethral region of the prostate at the age
of 9-18 months. Dietary soy partially inhibited the development of pr
ostatic dysplasia in these neonatally estrogenized animals, which may
be due to phytoestrogens contained in soy-rich food. Conclusion: Prost
atic cancer and its possible precursors develop spontaneously, or can
be induced by different chemical and hormonal manipulations in certain
animal species and strains. Neonatal estrogenization of the mouse res
ults in prostatic dysplasia, which can be partially prevented by dieta
ry soy. There are morphological similarities between human prostatic i
ntraepithelial neoplasia (PIN) and dysplastic changes in rodent prosta
tes, but more data is needed before these dysplastic lesions can be co
nsidered equivalent to human PIN.