Regulation of 3 beta-hydroxysteroid dehydrogenase type 1 and type 2 gene expression and function in the human ovarian surface epithelium by cytokines

Georgia Papacleovoulou, Kirsten Hogg, K Scott Fegan, Hilary O D Critchley, Stephen G Hillier, J Ian Mason

Research output: Contribution to journalArticlepeer-review

Abstract / Description of output

The human ovarian surface epithelium (hOSE) is a squamous-to-cuboidal layer that surrounds the ovary. hOSE undergoes injury and repair cycles as a result of ovulation-induced inflammation, an event relevant to the development of epithelial ovarian cancer (EOC). Locally produced steroids mediate the response to inflammation. 3 beta-Hydroxysteroid dehydrogenase (3 beta-HSD) drives the intracrine generation of progestogens and androgens that potentially affect cell survival and proliferation. We therefore investigated the regulation of 3 beta-HSD along with downstream steroid signalling in hOSE. Double immunofluorescence of cultured primary hOSE cells confirmed the expression of 3 beta-HSD protein Interleukin (IL). IL-1 alpha treatment of primary cells to mimic ovulation-associated inflammation suppressed 3 beta-HSD1 expression and stimulated 3 beta-HSD2 mRNA (P <0.001), without affecting total 3 beta-HSD protein and activity or androgen or progesterone receptor (PR) mRNA levels. Conversely, IL-4 as a proxy for a post-ovulatory healing cytokine increased both 3 beta-HSD transcripts, total protein and activity (P <0.01). IL-4 also suppressed androgen receptor expression (P <0.01) without affecting that of the PR, thereby potentially sustaining both progesterone biosynthesis and its underlying signalling in the ovarian surface. 3 beta-HSD protein was immunodetectable in primary ascites of women who were diagnosed with EOC but both mRNA transcripts were diminished relative to normal cells (P <0.05). Notably, this difference was countered by IL-4 treatment (P <0.01). We conclude that stimulation by IL-4 could be physiologically relevant to post-ovulatory ovarian healing and suggest a novel therapeutic strategy for the activation of progesterone-associated apoptosis in ovarian cancer. Also, our results suggest an attenuation of 3 beta-HSD expression in EOC although further studies are required for confirmation.
Original languageEnglish
Pages (from-to)379-392
Number of pages14
JournalMolecular Human Reproduction
Issue number6
Publication statusPublished - Jun 2009

Keywords / Materials (for Non-textual outputs)

  • human ovarian surface epithelium
  • 3beta-HSD
  • ovulation
  • cytokines
  • ovarian cancer


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