Literature DB >> 16955135

You say estren, I say estrogen. Let's call the whole replacement off!

Ushma S Neill1.   

Abstract

Estrogens and androgens play a key role in regulating bone mass. However, their clinical use as bone anabolic agents is limited due to unwanted side effects, particularly in reproductive organs. In 2002, the synthetic ligand estren was described to reproduce the bone anabolic, nongenotropic effects of sex steroids while having no effect on the uterus or seminal vesicles. But in the current issue of the JCI, Windahl et al. provide data showing that estrens are not as suitable a replacement for estrogen as was initially reported (see the related article beginning on page 2500). Though not catabolic, estrens triggered only minor, nonsignificant increases in bone mass in gonadectomized mice, all the while inducing hypertrophy of reproductive organs. Does this mean estrens should not be pursued as a therapy for osteoporosis?

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Year:  2006        PMID: 16955135      PMCID: PMC1555661          DOI: 10.1172/JCI29733

Source DB:  PubMed          Journal:  J Clin Invest        ISSN: 0021-9738            Impact factor:   14.808


  7 in total

1.  Estren is a selective estrogen receptor modulator with transcriptional activity.

Authors:  Sofia Movérare; Johanna Dahllund; Niklas Andersson; Ulrika Islander; Hans Carlsten; Jan-Ake Gustafsson; Stefan Nilsson; Claes Ohlsson
Journal:  Mol Pharmacol       Date:  2003-12       Impact factor: 4.436

2.  Bone protection by estrens occurs through non-tissue-selective activation of the androgen receptor.

Authors:  Sara H Windahl; René Galien; Riccardo Chiusaroli; Philippe Clément-Lacroix; Frederic Morvan; Liên Lepescheux; François Nique; William C Horne; Michèle Resche-Rigon; Roland Baron
Journal:  J Clin Invest       Date:  2006-09       Impact factor: 14.808

Review 3.  Estrogen deficiency and bone loss: an inflammatory tale.

Authors:  M Neale Weitzmann; Roberto Pacifici
Journal:  J Clin Invest       Date:  2006-05       Impact factor: 14.808

4.  Kinase-mediated regulation of common transcription factors accounts for the bone-protective effects of sex steroids.

Authors:  Stavroula Kousteni; Li Han; Jin-Ran Chen; Maria Almeida; Lilian I Plotkin; Teresita Bellido; Stavros C Manolagas
Journal:  J Clin Invest       Date:  2003-06       Impact factor: 14.808

Review 5.  Estrogen receptors and human disease.

Authors:  Bonnie J Deroo; Kenneth S Korach
Journal:  J Clin Invest       Date:  2006-03       Impact factor: 14.808

6.  Estren behaves as a weak estrogen rather than a nongenomic selective activator in the mouse uterus.

Authors:  Sylvia C Hewitt; Jennifer Collins; Sherry Grissom; Katherine Hamilton; Kenneth S Korach
Journal:  Endocrinology       Date:  2006-02-09       Impact factor: 4.736

7.  Reversal of bone loss in mice by nongenotropic signaling of sex steroids.

Authors:  S Kousteni; J R Chen; T Bellido; L Han; A A Ali; C A O'Brien; L Plotkin; Q Fu; A T Mancino; Y Wen; A M Vertino; C C Powers; S A Stewart; R Ebert; A M Parfitt; R S Weinstein; R L Jilka; S C Manolagas
Journal:  Science       Date:  2002-10-25       Impact factor: 47.728

  7 in total
  1 in total

1.  Tissue selectivity of the anabolic steroid, 19-nor-4-androstenediol-3beta,17beta-diol in male Sprague Dawley rats: selective stimulation of muscle mass and bone mineral density relative to prostate mass.

Authors:  Stephanie T Page; Brett T Marck; James M Tolliver; Alvin M Matsumoto
Journal:  Endocrinology       Date:  2007-12-20       Impact factor: 4.736

  1 in total

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