P450Arom induction in isolated control endometrial cells by peritoneal fluid from women with endometriosis

Fertil Steril. 2010 Dec;94(7):2521-7. doi: 10.1016/j.fertnstert.2010.03.036. Epub 2010 Apr 28.

Abstract

Objective: To study the effect of peritoneal fluid from women with (PF-E) and without (PF-C) endometriosis on P(450)Arom expression in endometrial cells.

Design: Experimental study.

Setting: University research unit.

Patient(s): Forty women of reproductive age with (n = 22) or without (control; n = 18) endometriosis.

Intervention(s): Peritoneal fluid and eutopic endometrial samples were obtained during surgery from women with (n = 13 and 9, respectively) and without (n = 4 and 14, respectively) endometriosis.

Main outcome measure(s): Expression study for P(450)Arom, steroid factor 1 (SF-1), chicken ovalbumin upstream transcription factor I (COUP-TFI), and COUP-TFII messenger RNA (reverse transcriptase-polymerase chain reacion) and/or protein (immunoblot) in isolated endometrial epithelial cells transfected or not with expression vector containing SF-1, COUP-TFI, or COUP-TFII complementary DNAs.

Result(s): Basal messenger RNA and/or protein expression of P(450)Arom and SF-1 were augmented in endometriosis, and that of COUP-TF was diminished. In control cells, (Bu)(2)cAMP and PF-E increased P(450)Arom and SF-1 expression (but not COUP-TF expression) in a dose-dependent way, an effect not observed with PF-C, adsorbed PF-E, or 10(-5) M indomethacin. Transfected cells confirmed these results. Any treatments modified the studied molecules in endometriosis cells.

Conclusion(s): These data indicate that molecules contained in PF-E favor an estrogenic microenvironment, suggesting a role in the etiopathogenesis of endometriosis enabling the survival, maintenance, and growth of endometrial implants in the ectopic locations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aromatase / biosynthesis*
  • Aromatase / genetics
  • Ascitic Fluid / pathology*
  • Ascitic Fluid / physiology*
  • COUP Transcription Factors / genetics
  • COUP Transcription Factors / metabolism
  • Case-Control Studies
  • Cell Separation
  • Cells, Cultured
  • Endometriosis / metabolism
  • Endometriosis / pathology*
  • Endometrium / cytology
  • Endometrium / drug effects
  • Endometrium / enzymology
  • Endometrium / metabolism*
  • Enzyme Induction
  • Female
  • Humans
  • Middle Aged
  • Peritoneal Diseases / metabolism
  • Peritoneal Diseases / pathology*
  • Steroidogenic Factor 1 / genetics
  • Steroidogenic Factor 1 / metabolism

Substances

  • COUP Transcription Factors
  • NR5A1 protein, human
  • Steroidogenic Factor 1
  • Aromatase