Estren Is a Selective Estrogen Receptor Modulator with Transcriptional Activity

Sofia Movérare, Johanna Dahllund, Niklas Andersson, Ulrika Islander, Hans Carlsten, Jan-Ake Gustafsson, Stefan Nilsson, Claes Ohlsson

Research output: Contribution to journalArticle

21 Scopus citations

Abstract

It was recently reported that the synthetic compound estren increases bone mass without affecting reproductive organs or classic transcription. The aim of the present study was to further characterize the in vivo and in vitro effects of estren. We demonstrate that estren is a selective estrogen receptor modulator (SERM) with a strong effect on thymus, a moderate effect on uterus and trabecular bone, but no major effect on fat or cortical bone in 11-month-old ovariectomized mice. The effect of estren on trabecular bone and uterus is mediated via estrogen receptors (ERs) because no effect is seen in ER double-inactivated mice. Furthermore, with the use of ERα- and ERβ-expressing reporter cell lines, we demonstrate that estren displays an agonistic effect on transcriptional activity of an estrogen-responsive element-driven reporter gene with a degree of agonism similar to that of 17β-estradiol for both ERα and ERβ. Thus, estren has the capacity to exert genomic effects via both ERα and ERβ. We conclude, in contrast to what was previously reported by others, that estren is a SERM with transcriptional activity.

Original languageEnglish (US)
Pages (from-to)1428-1433
Number of pages6
JournalMolecular Pharmacology
Volume64
Issue number6
DOIs
StatePublished - Dec 1 2003

ASJC Scopus subject areas

  • Molecular Medicine
  • Pharmacology

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