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Publication : Aggressive prostate cancer is prevented in ERαKO mice and stimulated in ERβKO TRAMP mice.

First Author  Slusarz A Year  2012
Journal  Endocrinology Volume  153
Issue  9 Pages  4160-70
PubMed ID  22753646 Mgi Jnum  J:189182
Mgi Id  MGI:5444580 Doi  10.1210/en.2012-1030
Citation  Slusarz A, et al. (2012) Aggressive prostate cancer is prevented in ERalphaKO mice and stimulated in ERbetaKO TRAMP mice. Endocrinology 153(9):4160-70
abstractText  Previous evidence suggests soy genistein may be protective against prostate cancer, but whether this protection involves an estrogen receptor (ER)-dependent mechanism is unknown. To test the hypothesis that phytoestrogens may act through ERalpha or ERbeta to play a protective role against prostate cancer, we bred transgenic mice lacking functional ERalpha or ERbeta with transgenic adenocarcinoma of mouse prostate (TRAMP) mice. Dietary genistein reduced the incidence of cancer in ER wild-type (WT)/transgenic adenocarcinoma of mouse prostate mice but not in ERalpha knockout (KO) or ERbetaKO mice. Cancer incidence was 70% in ERWT mice fed the control diet compared with 47% in ERWT mice fed low-dose genistein (300 mg/kg) and 32% on the high-dose genistein (750 mg/kg). Surprisingly, genistein only affected the well differentiated carcinoma (WDC) incidence but had no effect on poorly differentiated carcinoma (PDC). No dietary effects have been observed in either of the ERKO animals. We observed a very strong genotypic influence on PDC incidence, a protective effect in ERalphaKO (only 5% developed PDC), compared with 19% in the ERWT, and an increase in the incidence of PDC in ERbetaKO mice to 41%. Interestingly, immunohistochemical analysis showed ERalpha expression changing from nonnuclear in WDC to nuclear in PDC, with little change in ERbeta location or expression. In conclusion, genistein is able to inhibit WDC in the presence of both ERs, but the effect of estrogen signaling on PDC is dominant over any dietary treatment, suggesting that improved differential targeting of ERalpha vs. ERbeta would result in prevention of advanced prostate cancer.
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