Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/41974
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dc.contributor.authorBirrell, S.en
dc.contributor.authorButler, L.en
dc.contributor.authorHarris, J.en
dc.contributor.authorBuchanan, G.en
dc.contributor.authorTilley, W.en
dc.date.issued2007en
dc.identifier.citationFASEB Journal, 2007; 21(10):2285-2293en
dc.identifier.issn0892-6638en
dc.identifier.issn1530-6860en
dc.identifier.urihttp://hdl.handle.net/2440/41974-
dc.descriptionCopyright © 2007 by The Federation of American Societies for Experimental Biologyen
dc.description.abstractThere is now considerable evidence that using a combination of synthetic progestins and estrogens in hormone replacement therapy (HRT) increases the risk of breast cancer compared with estrogen alone. Furthermore, the World Health Organization has recently cited combination contraceptives, which contain synthetic progestins, as potentially carcinogenic to humans, particularly for increased breast cancer risk. Given the above observations and the current trend toward progestin-only contraception, it is important that we have a comprehensive understanding of how progestins act in the millions of women worldwide who regularly take these medications. While synthetic progestins, such as medroxyprogesterone acetate (MPA), which are currently used in both HRT and oral contraceptives were designed to act exclusively through the progesterone receptor, it is clear from both clinical and experimental settings that their effects may be mediated, in part, by binding to the androgen receptor (AR). Disruption of androgen action by synthetic progestins may have serious deleterious side effects in the breast, where the balance between estrogen signaling and androgen signaling plays a critical role in breast homeostasis. Here, we review the role of androgen signaling in the normal breast and in breast cancer and present new data demonstrating that androgen receptor function can be perturbed by low doses of MPA, similar to doses achieved in serum of women taking HRT. We propose that the observed excess of breast malignancies associated with combined HRT may be explained, in part, by synthetic progestins such as MPA acting as endocrine disruptors to negate the protective effects of androgen signaling in the breast. Understanding the role of androgen signaling in the breast and how this is modulated by synthetic progestins is necessary to determine how combined HRT alters breast cancer risk, and to inform the development of optimal preventive and treatment strategies for this disease.en
dc.description.statementofresponsibilityStephen N. Birrell, Lisa M. Butler, Jonathan M. Harris, Grant Buchanan and Wayne D. Tilleyen
dc.language.isoenen
dc.publisherFederation Amer Soc Exp Biolen
dc.subjecthormone replacement therapy; medroxyprogesterone acetate; estrogen signalingen
dc.titleDisruption of androgen receptor signaling by synthetic progestins may increase risk of developing breast canceren
dc.typeJournal articleen
dc.identifier.rmid0020072268en
dc.identifier.doi10.1096/fj.06-7518comen
dc.identifier.pubid47802-
pubs.library.collectionMedicine publicationsen
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
dc.identifier.orcidBirrell, S. [0000-0002-1023-413X]en
dc.identifier.orcidButler, L. [0000-0003-2698-3220]en
dc.identifier.orcidTilley, W. [0000-0003-1893-2626]en
Appears in Collections:Medicine publications

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