All-trans-retinoic acid mediates changes in PI3K and retinoic acid signaling proteins of leiomyomas

Fertil Steril. 2011 May;95(6):2080-6. doi: 10.1016/j.fertnstert.2011.01.155. Epub 2011 Feb 26.

Abstract

Objective: To detect changes induced by all-trans-retinoic acid (ATRA) on the expression and activation of target proteins of the retinoic acid (RA) and PI3K/Akt pathways involved in leiomyoma growth.

Design: A study on human tissue cultures.

Setting: Hadassah University Hospital.

Patient(s): Premenopausal women with uterine leiomyomas.

Intervention(s): Paired cultures of normal myometrium and leiomyomas, from women undergoing hysterectomy, were obtained.

Main outcome measure(s): The effect of ATRA was examined on the expression and phosphorylation of relevant RA, PI3K/Akt, and Bcl2 proteins (immunochemical analysis), cell proliferation, cell cycle distribution, and apoptosis.

Result(s): Applying our cell culture model, we demonstrated that ATRA induced changes in the expression and activation of the RA and PI3K/Akt pathway proteins in leiomyoma cells, with significant increases of alcohol dehydrogenase 1 and cyclin D2 protein levels. In part of the leiomyoma cells, ATRA induced a relative increase of Bax (proapoptotic) as well as a relative decrease of phosphorylated glycogen synthase kinase 3β (proapoptotic).

Conclusion(s): Our results highlight the involvement of ATRA in the RA and PI3K/Akt pathways, whose specific signaling products may influence the outcome of leiomyoma growth by regulating cell proliferation, apoptosis, and survival. These results might be useful for the on-going research into alternative methods for treating and preventing this disorder.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Apoptosis / drug effects
  • Cell Cycle / drug effects
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Drug Evaluation, Preclinical
  • Female
  • Humans
  • Leiomyoma / metabolism*
  • Leiomyoma / pathology
  • Matched-Pair Analysis
  • Middle Aged
  • Models, Biological
  • Phosphatidylinositol 3-Kinases / metabolism*
  • Receptors, Retinoic Acid / metabolism
  • Signal Transduction / drug effects
  • Signal Transduction / physiology
  • Tretinoin / metabolism*
  • Tretinoin / pharmacology*
  • Uterine Neoplasms / metabolism*
  • Uterine Neoplasms / pathology

Substances

  • Receptors, Retinoic Acid
  • Tretinoin
  • Phosphatidylinositol 3-Kinases