Molecular analysis of human endometrium: Short-term tibolone signaling differs significantly from estrogen and estrogen + progestagen signaling
Journal of Molecular Medicine , Volume 85 - Issue 5 p. 471- 480
Tibolone, a tissue-selective compound with a combination of estrogenic, progestagenic, and androgenic properties, is used as an alternative for estrogen or estrogen plus progesterone hormone therapy for the treatment of symptoms associated with menopause and osteoporosis. The current study compares the endometrial gene expression profiles after short-term (21 days) treatment with tibolone to the profiles after treatment with estradiol-only (E2) and E2+ medroxyprogesterone acetate (E2+ MPA) in healthy postmenopausal women undergoing hysterectomy for endometrial prolapse. The impact of E2treatment on endometrial gene expression (799 genes) was much higher than the effect of tibolone (173 genes) or E2+ MPA treatment (174 genes). Furthermore, endometrial gene expression profiles after tibolone treatment show a weak similarity to the profiles after E2treatment (overlap 72 genes) and even less profile similarity to E2+ MPA treatment (overlap 17 genes). Interestingly, 95 tibolone-specific genes were identified. Translation of profile similarity into biological processes and pathways showed that ER-mediated downstream processes, such as cell cycle and cell proliferation, are not affected by E2 + MPA, slightly by tibolone, but are significantly affected by E2. In conclusion, tibolone treatment results in a tibolone-specific gene expression profile in the human endometrium, which shares only limited resemblance to E2and even less resemblance to E2 + MPA induced profiles.
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|Journal of Molecular Medicine|
|Organisation||Erasmus MC: University Medical Center Rotterdam|
Hanifi-Moghaddam, P, Boers-Sijmons, B, Klaassens, A.H.A, van Wijk, F.H, den Bakker, M.A, Ott, M.C, … Blok, L.J. (2007). Molecular analysis of human endometrium: Short-term tibolone signaling differs significantly from estrogen and estrogen + progestagen signaling. Journal of Molecular Medicine, 85(5), 471–480. doi:10.1007/s00109-006-0146-1