RT Journal Article SR Electronic T1 Stimulation of Endometrial Glandular Cells with Genistein and Daidzein and their Effects on ERα- and ERβ-mRNA and Protein Expresion JF Anticancer Research JO Anticancer Res FD International Institute of Anticancer Research SP 1713 OP 1718 VO 25 IS 3A A1 STEFANIE STAAR A1 DAGMAR-ULRIKE RICHTER A1 JOSEF MAKOVITZKY A1 VOLKER BRIESE A1 CLAUDIA BERGEMANN YR 2005 UL http://ar.iiarjournals.org/content/25/3A/1713.abstract AB Phytoestrogens seem to have estrogen-like effects in the human body as their structure is very similar to those estrogens produced in human glands. The aim of the present study was to analyse the effects of genistein and daidzein on estrogen receptor (ER)α- and ERβ-mRNA and protein expression in the endometrium of premenopausal women. Materials and Methods: Glandular endometrial cells were isolated from endometrial biopsies obtained from regularly menstruating women undergoing gynaecological abrasio or hysterectomy. Cells were stimulated with single doses of genistein or daidzein. ERα- and ERβ-protein expression were determined by immunocytochemical analysis. In addition ERα- and ERβ-mRNA expression were determined by quantitative real-time RT-PCR. Quantification was carried out by the ΔΔCT-method using glyceraldehyde phosphate dehydrogenase (GAPDH) as housekeeping gene. Results: Endometrial glandular cells responded to stimulation with genistein and daidzein by alteration of both ERα- and ERβ-mRNA expression. The effects were time- and dose-dependent. Detection of ERα- and ERβ-protein expression by immunocytochemistry showed a dose-dependent regulation after stimulation of isolated endometrial cells with phytoestrogens. Discussion: According to our results, we suggest that ER expression in endometrial glandular cells is regulated by genistein and daidzein on the mRNA and protein levels. We could detect a decrease in ERα- and an increase in ERβ-mRNA expression after stimulation with tested phytoestrogens. Our results are in line with findings that phytoestrogens act as anti-estrogens in organs expressing more ERα and as estrogens in ERβ-presenting organs.