Tamoxifen

From OpenWetWare

Revision as of 04:33, 6 April 2009 by Jakob Suckale (Talk | contribs)
Jump to: navigation, search
chemical structure of tamoxifen
chemical structure of tamoxifen

Tamoxifen is a common breast cancer drug (Nolvadex, Istubal, and Valodex). In molecular biology tamoxifen activates enzymes inactivated by fusion to a modified estrogen receptor (ER). This is employed, for example, in the timed activation of Cre recombinase in CreER mice.

Contents

Molecular mechanism of action

Tamoxifen competitively binds to GPCR type and intracellular type estrogen receptors (ER). Binding to the intracellular ER on tumours and other tissue targets produces a nuclear complex that decreases DNA synthesis and inhibits estrogen effects (diagram of estrogen & tamoxifen mechanism). It thus acts as an estrogen antagonists which inhibits the growth of some tumours dependent on estrogen stimulation.

Tamoxifen itself is a prodrug, having relatively little affinity for the estrogen receptor. It is metabolised in the liver by the cytochrome P450 to active metabolites such as 4-hydroxytamoxifen and N-desmethyl-4-hydroxytamoxifen.

Activation of ER-fusion proteins

Proteins fused to an estrogen receptor (ER) domain are sequestered by heat shock proteins (hsp). Administration of tamoxifen to an often modified ER with increased affinity for tamoxifen over the natural substrate estrogen, releases the fusion protein. In the case of an enzyme-ER fusion, like CreER, it can than act on its substrate.

Stability & storage

Chemical stability (tamoxifen citrate [1])

  • stable for at least 2 years when stored desiccated at 2-8°C in the dark
  • hygroscopic at high relative humidities
  • sensitive to UV light

Metabolism

  • distribution half-life: 7-14 hours
  • elimination half-life: 5-7 days (range: 3-21 days)
  • elimination half-life of N-desmethyltamoxifen (major metabolite): 9-14 days

(estimates based on limited data probably from humans [2])

Protocols using tamoxifen

  • [Tamoxifen administration to mice]

See also

Personal tools