Effect of hormonal agents on monocyte chemotactic protein-1 expression by endometrial epithelial cells of women with endometriosis

Citation
A. Boucher et al., Effect of hormonal agents on monocyte chemotactic protein-1 expression by endometrial epithelial cells of women with endometriosis, FERT STERIL, 74(5), 2000, pp. 969-975
Citations number
46
Categorie Soggetti
Reproductive Medicine","da verificare
Journal title
FERTILITY AND STERILITY
ISSN journal
00150282 → ACNP
Volume
74
Issue
5
Year of publication
2000
Pages
969 - 975
Database
ISI
SICI code
0015-0282(200011)74:5<969:EOHAOM>2.0.ZU;2-M
Abstract
Objective: To assess whether hormonal agents used in the medical treatment of endometriosis, such as danazol and GnRH agonist, exert direct regulatory action on monocyte chemotactic protein-1 (MCP-I) expression by endometrial epithelial cells. Design: Primary cultures of epithelial cells isolated from human endometriu m were exposed to different concentrations of cytokines and steroid hormone analogs. Expression of MCP-1 was analyzed at the levels of protein and mes senger RNA. Setting: Gynecology clinic and laboratory of endocrinology of r eproduction. Patient(s): Women presenting for infertility or pelvic pain in whom endomet riosis was diagnosed by using laparoscopy. Intervention(s): Endometrial tissue biopsy performed at laparoscopy. Main Outcome Measure(s): Secretion of MCP-1 protein was measured by using e nzyme-linked immunosorbent assay, and mRNA steady-state levels were measure d by performing Northern blot analysis. Results: Buserelin acetate, a GnRH agonist (0.1-10 ng/mL), had no significa nt effect on MCP-1 expression, whereas danazol (10(-7)-10(-5) M), a testost erone analog, and dexamethasone, an anti-inflammatory glucocorticoid hormon e (10(-12)-10(-6) M), showed a direct and a dose-dependent inhibitory effec t on MCP-1 expression. This effect occurred at the level of protein and mRN A. Conclusion(s): The findings of the study may affect understanding of the me chanisms by which hormonal treatments act on endometriosis and influence it s clinical manifestations. (C) 894 by American Society for Reproductive Med icine.