Dephosphorylation of oestradiol nuclear receptor in vitro. A hypothesis on the mechanism of action of non-steroidal anti-oestrogens

Biochem J. 1981 Sep 15;198(3):699-702. doi: 10.1042/bj1980699.

Abstract

We show that a mouse uterus nuclear phosphatase exists that is capable of inactivating nuclear oestrogen receptor complexed to oestradiol-17 beta in vitro but is ineffective when the receptor is complexed with the two non-steroidal anti-oestrogens, nafoxidine and tamoxifen. We suggest that the long half-life of the tamoxifen-receptor complex versus the short half-life of the oestradiol-receptor complex in uterine nuclei in vivo is the result of the ineffectiveness of the phosphatase in dephosphorylating the anti-oestrogen-receptor complex.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cattle
  • Cell Nucleus / drug effects
  • Cell Nucleus / enzymology
  • Cell Nucleus / metabolism
  • Cytosol / metabolism
  • Estradiol / metabolism
  • Female
  • Half-Life
  • In Vitro Techniques
  • Mice
  • Nafoxidine / pharmacology*
  • Phosphoric Monoester Hydrolases / metabolism
  • Pyrrolidines / pharmacology*
  • Receptors, Estradiol
  • Receptors, Estrogen / drug effects*
  • Tamoxifen / pharmacology*
  • Uterus / drug effects
  • Uterus / metabolism*

Substances

  • Pyrrolidines
  • Receptors, Estradiol
  • Receptors, Estrogen
  • Tamoxifen
  • Nafoxidine
  • Estradiol
  • Phosphoric Monoester Hydrolases