Abstract

The human estrogen receptor alpha-isoform (ERalpha) is a nuclear transcription factor that displays a complex pharmacology. In addition to classical agonists and antagonists, the transcriptional activity of ERalpha can be regulated by selective estrogen receptor modulators, a new class of drugs whose relative agonist/antagonist activity is determined by cell context. It has been demonstrated that the binding of different ligands to ERalpha results in the formation of unique ERalpha-ligand conformations. These conformations have been shown to influence ERalpha-cofactor binding and, therefore, have a profound impact on ERalpha pharmacology. In this study, we demonstrate that the nature of the bound ligand also influences the stability of ERalpha, revealing an additional mechanism by which the pharmacological activity of a compound is determined. Of note we found that although all ERalpha-ligand complexes can be ubiquitinated and degraded by the 26 S proteasome in vivo, the mechanisms by which they are targeted for proteolysis appear to be different. Specifically, for agonist-activated ERalpha, an inverse relationship between transcriptional activity and receptor stability was observed. This relationship does not extend to selective estrogen receptor modulators and pure antagonists. Instead, it appears that with these compounds, the determinant of receptor stability is the ligand-induced conformation of ERalpha. We conclude that the different conformational states adopted by ERalpha in the presence of different ligands influence transcriptional activity directly by regulating cofactor binding and indirectly by modulating receptor stability.

Highlights

  • estrogen receptor ␣-isoform (ER␣)1 resides within the nuclei of target cells in an inactive form in the absence of hormone

  • It has been speculated that recruitment of coactivators like SRC-1 may be a rate-limiting step in this pathway [21], the mechanism(s) by which estradiol-activated ER␣ is recognized by the 26 S proteasome remains to be determined

  • We evaluated the effect of short term treatment (4 h) with a variety of ER␣ ligands on the relative expression level of endogenous ER␣ within MCF-7 cells, using Western immunoblot analysis

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Summary

The abbreviations used are

ER␣, estrogen receptor ␣-isoform; SERM, selective estrogen receptor modulator; PAGE, polyacrylamide gel electrophoresis. In this study, we have performed a series of experiments to 1) evaluate the influence of ER␣ agonists, antagonists, and SERMs on the stability of the human ER␣ and 2) probe potential correlations between ligand-induced receptor stability and the relative agonist/antagonist activity of an individual compound. Information of this nature will help us to define the mechanisms underlying the agonist/antagonist activity of ER␣-ligands and will be useful in the design of screens for ER␣-ligands with unique pharmacological attributes

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