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Effects of mifepristone on vascular endothelial growth factor and thrombospondin-1 mRNA in Ishikawa cells: implication for the endometrial effects of mifepristone.

Abstract
Mifepristone has been used for both medical termination of pregnancy and emergency contraception. Mifepristone may have both an antiovulatory activity and an antiproliferative effect on the endometrium. We have evaluated the effect of mifepristone on vascular endothelial growth factor (VEGF) and thrombospondin-1 (TSP-1) using Ishikawa cells in vitro. Mifepristone, progesterone and 17beta-estradiol at concentrations of 1.0, 0.1 and 0.01 microM, were added to confluent cells and further cultured for additional 24 h. Total RNA was extracted from control and treated cells. After reverse transcription, VEGF, TSP-1 and beta-actin cDNAs were amplified with polymerase chain reaction spiked with 33p-dCTP. The relative abundance of VEGF 121 and 165 isoforms and TSP-1 mRNA were measured by scintillation spectroscopy. Mifepristone and progesterone did not stimulate VEGF mRNA 121 and 165 isoforms, while 17beta-estradiol increased both VEGF isoforms. Mifepristone did not stimulate TSP-1 mRNA at any concentration, but progesterone increased TSP-1 mRNA, and this effect was inhibited with mifepristone. 17beta-Estradiol did not increase TSP-1 expression. We hypothesized, based on these data, that the clinical finding of endometrial antiproliferative effect and low vaginal bleeding rate observed in women using mifepristone may be related to lack of stimulation of these angiogenic factors.
AuthorsSebastian Mirkin, David F Archer
JournalContraception (Contraception) Vol. 70 Issue 4 Pg. 327-33 (Oct 2004) ISSN: 0010-7824 [Print] United States
PMID15451338 (Publication Type: Journal Article)
CopyrightCopyright 2004 Elsevier Inc.
Chemical References
  • Contraceptives, Oral, Synthetic
  • Hormone Antagonists
  • RNA, Messenger
  • Thrombospondin 1
  • Vascular Endothelial Growth Factor A
  • Mifepristone
  • Progesterone
  • Estradiol
Topics
  • Adenocarcinoma
  • Cell Line
  • Contraceptives, Oral, Synthetic (pharmacology)
  • Dose-Response Relationship, Drug
  • Endometrial Neoplasms
  • Endometrium (drug effects)
  • Epithelial Cells
  • Estradiol (administration & dosage, pharmacology)
  • Female
  • Gene Expression (drug effects)
  • Hormone Antagonists (pharmacology)
  • Humans
  • Mifepristone (administration & dosage, pharmacology)
  • Progesterone (administration & dosage, pharmacology)
  • RNA, Messenger (analysis)
  • Thrombospondin 1 (genetics)
  • Tumor Cells, Cultured
  • Vascular Endothelial Growth Factor A (genetics)

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