Abstract

Objective: To quantify messenger RNA (mRNA) levels of the two estrogen receptor isoforms, estrogen receptor-α (ER-α) and estrogen receptor-β (ER-β) in the eutopic endometrium and ovarian endometriotic cysts. Design: Prospective study. Setting: University hospital. Patient(s): Patients with endometriosis and patients with uterine leiomyoma or carcinoma in situ. Intervention(s): Gonadotropin-releasing hormone agonist (GnRH-a)-treated (n = 12) or untreated (n = 24) endometriotic cysts were obtained from 36 patients during laparoscopic cystectomy. Eutopic endometrium tissues were obtained from 24 patients during or immediately after surgery. Main Outcome Measure(s): ER-α and ER-β mRNA levels, using a real-time reverse transcription (RT)-polymerase chain reaction (PCR) assay, TaqMan RT-PCR. Result(s): Eutopic endometrium and ovarian endometriotic cysts showed predominantly higher levels of ER-α mRNA than ER-β mRNA. Although ER-α and ER-β mRNA levels in the eutopic endometrium were affected by a cyclic change in ovarian hormones, ovarian endometriotic cysts were less affected. Moreover, a long-term hypoestrogenic state induced by GnRH-a especially decreased ER-α mRNA levels in endometriotic cysts. Consequently, the relative ratios of ER-α to ER-β mRNA levels in both GnRH-a-treated and untreated endometriotic cysts were significantly lower than those in the eutopic endometrium. Conclusion(s): The results suggest that the principal and regulatory effects of estrogens may be mediated mainly via ER-α rather than ER-β in both the eutopic endometrium and endometriotic cysts.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.