
TY  - JOUR
A1  - Cunha, Gerald R. 
A1  - Wang, Y. Z. 
A1  - Hayward, Simon W. 
A1  - Risbridger, Gail P. 
T1  - Estrogenic effects on prostatic differentiation and carcinogenesis
JF  - Reproduction, Fertility and Development
JO  - Reprod. Fertil. Dev.
Y1  - 2001
VL  - 13
IS  - 4
SP  - 285
EP  - 296
KW  - 
UR  - https://doi.org/10.1071/RD01010 
N2  - Estrogens, alone or in combination with androgens, can induce aberrant growth and/or malignancy of the prostate gland. Squamous metaplasia is an abnormal form of prostatic epithelial differentiation elicited by exogenous estrogen alone. Estrogens elicit their effects via estrogen receptors (ER) in the prostate. Experiments using ER&#945; and ER&#946; null mice demonstrated that ER&#945;, but not ER&#946; is essential in the induction of prostatic squamous metaplasia. To determine the respective roles of epithelial versus stromal ER&#945; in this response, the following tissue recombinants were constructed with prostatic epithelium (PRE) and stroma (S) from wild-type (wt) and ER&#945; knockout (&#945;ERKO) mice: wt-S + wt-PRE, &#183; &#945;ERKO-S + &#945;ERKO-PRE, wt-S + &#945;ERKO-PRE and &#945;ERKO-S + wt-PRE. A metaplastic response to diethylstilbestrol (DES) was only observed in wt-S + wt-PRE tissue recombinants. Tissue recombinants containing &#945;ERKO-PRE and/or &#945;ERKO-S (ERKO-S + &#945;ERKO-PRE, wt-S + &#945;ERKO-PRE and &#945;ERKO-S + wt-PRE) failed to respond to DES. Therefore, full and uniform epithelial squamous metaplasia requires ER&#945; in both the epithelium and stroma. Estradiol (E2) in combination with testosterone (T) was shown to be effective in inducing prostatic carcinogenesis in a tissue recombinant model composed of rat urogenital sinus mesenchyme plus mouse prostatic epithelium. A particularly efficient model of prostatic carcinogenesis in mice involves T + E2 treatment of mice bearing grafts of wild-type rat urogenital mesenchyme (rUGM) plus retinoblastoma gene (Rb) knockout (Rb-KO) prostatic epithelium (rUGM + Rb-KO-PRE). Such rUGM + Rb-KO-PRE tissue recombinants developed hyperplasia, atypical hyperplasia and invasive prostatic carcinoma with high efficiency. During carcinogenesis in rUGM + Rb-KO-PRE tissue recombinants, epithelial E-cadherin almost totally disappeared and epithelial PCNA labeling was elevated. These epithelial changes were associated with almost total loss of smooth muscle cells in the stroma. The results of this study demonstrate that the absence of the Rb tumor suppressor gene predisposes prostatic epithelial cells to hormonal carcinogenesis. 
ER  -

