Endometrial expression of the estrogen-sensitive genes MMP-26 and TIMP-4 is altered by a substitution protocol without down-regulation in IVF patients
Language English Country Great Britain, England Media print-electronic
Document type Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't
PubMed
17012332
DOI
10.1093/humrep/del180
PII: del180
Knihovny.cz E-resources
- MeSH
- Estrogen Receptor alpha metabolism MeSH
- Adult MeSH
- Down-Regulation * MeSH
- Endometrium metabolism MeSH
- Estrogens pharmacology MeSH
- Fertilization in Vitro * MeSH
- Humans MeSH
- Menstrual Cycle metabolism MeSH
- Matrix Metalloproteinases, Secreted genetics metabolism MeSH
- Receptors, Progesterone metabolism MeSH
- Gene Expression Regulation MeSH
- Tissue Inhibitor of Metalloproteinases genetics metabolism MeSH
- Tissue Inhibitor of Metalloproteinase-4 MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Estrogen Receptor alpha MeSH
- Estrogens MeSH
- Matrix Metalloproteinases, Secreted MeSH
- MMP26 protein, human MeSH Browser
- Receptors, Progesterone MeSH
- Tissue Inhibitor of Metalloproteinases MeSH
BACKGROUND: The aim of this study was to analyse the effects of an estradiol (E(2))-progesterone substitution protocol on the endometrial expression of estrogen-sensitive genes during the peri-implantation period. METHODS: Peripheral blood and endometrial biopsies were obtained from 13 infertile women both in a natural cycle (NC), on days 5 and 7 after ovulation (NC5, NC7), and in an artificial (substituted) cycle (AC), on days 5 and 7 of progesterone addition (AC5, AC7). Estrogen receptor-alpha (ERalpha) and progesterone receptor (PR) were assayed by immunohistochemistry. Matrix metalloproteinase-26 (MMP-26) mRNA and tissue inhibitor of metalloproteinase-4 (TIMP-4) mRNA were semiquantitatively assessed in tissue sections using in situ hybridization (ISH) and quantified in tissue extracts using real-time PCR. RESULTS: Levels of both E(2) and progesterone were higher in the peripheral blood in AC than in NC. Also on day AC5, expressions of ERalpha, PR and MMP-26 mRNA (focally) were increased in the epithelium and TIMP-4 mRNA in the stroma. Expression levels of these genes dropped significantly between AC5 and AC7, but not between NC5 and NC7. Abnormally high levels in AC5 samples suggest overstimulation with E(2), and the rapid decrease between AC5 and AC7 suggests overstimulation with progesterone. CONCLUSIONS: In ACs, increased levels of E(2) in the blood exaggerate the endometrial expression of estrogen-sensitive genes, whereas higher levels of progesterone in the blood in the secretory phase exaggerate the drop in expression of these genes. Dramatic variations in the gene expression may not be optimal for the implantation process.
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