The immninent dawn of SPRMs in obstetrics and gynecology

Mol Cell Endocrinol. 2012 Jul 25;358(2):232-43. doi: 10.1016/j.mce.2012.02.021. Epub 2012 Mar 10.

Abstract

Selective progesterone receptor modulators (SPRMs) have been developed since the late 70s when mifepristone was first described. They act through nuclear progesterone receptors and can have agonist or mixed agonist antagonist actions depending on the cell and tissue. Mifepristone has unique major antagonist properties allowing its use for pregnancy termination. Ulipristal acetate has been marketed in 2009 for emergency contraception and has been recently approved for preoperative myoma treatment. Further perspectives for SPRMs use include long term estrogen free contraception, endometriosis treatment. However long term applications will be possible only after confirmation of endometrial safety.

Publication types

  • Review

MeSH terms

  • Contraception
  • Female
  • Gynecology*
  • Hormone Antagonists / adverse effects
  • Hormone Antagonists / chemistry
  • Hormone Antagonists / pharmacology*
  • Humans
  • Mifepristone / adverse effects
  • Mifepristone / chemistry
  • Mifepristone / pharmacology
  • Obstetrics*
  • Receptors, Progesterone / agonists
  • Receptors, Progesterone / antagonists & inhibitors

Substances

  • Hormone Antagonists
  • Receptors, Progesterone
  • Mifepristone