Expression of GnRH receptor gene in human ectopic endometrial cells and inhibition of their proliferation by leuprolide acetate

Citation
R. Borroni et al., Expression of GnRH receptor gene in human ectopic endometrial cells and inhibition of their proliferation by leuprolide acetate, MOL C ENDOC, 159(1-2), 2000, pp. 37-43
Citations number
27
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
MOLECULAR AND CELLULAR ENDOCRINOLOGY
ISSN journal
03037207 → ACNP
Volume
159
Issue
1-2
Year of publication
2000
Pages
37 - 43
Database
ISI
SICI code
0303-7207(20000125)159:1-2<37:EOGRGI>2.0.ZU;2-C
Abstract
The present study was conducted to investigate whether GnRH-receptor (GnRH- R) gene is expressed in endometriosis ovarian implants and whether a GnRH-a nalogue (GnRH-a) may exert an effect on endometriosis cell proliferation in vitro. The presence of GnRH-R transcripts in ovarian endometriosis cells w as assessed by reverse transcription-polymerase chain reaction (RT-PCR) and further confirmed by Southern blot analysis. GnRH-R mRNA was detected in a ll the 13 samples examined. In contrast, GnRH-R transcripts were not detect able in endometriosis-free peritoneal tissue. In the second part of the stu dy, endometriosis cells were cultured for 9 days with different doses of le uprolide acetate (ranging from 0 to 10(-5) M). In 4 out of 13 cases, a sign ificant anti-proliferative effect was observed at doses of leuprolide aceta te ranging from 10(-9) to 10(-5) M. In one case, a significant inhibition o f cell proliferation was observed only at 10-5 M leuprolide acetate concent ration. In contrast, the GnRH-a did not affect cell growth, regardless of t he expression of GnRH-R transcripts and the given doses, in the remaining 8 experiments. To date, this is the first evidence indicating that GnRH-R mR NA is expressed in human ovarian endometriomas. Moreover, the inhibition of endometriosis cell proliferation induced by the GnRH-a in vitro suggests t hat, at least in some cases, this compound might exert a direct effect on e ndometriosis lesions. (C) 2000 Elsevier Science Ireland Ltd. All rights res erved.