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dc.contributor.authorPeters, KM
dc.contributor.authorEdwards, SL
dc.contributor.authorNair, SS
dc.contributor.authorFrench, JD
dc.contributor.authorBailey, PJ
dc.contributor.authorSalkield, K
dc.contributor.authorStein, S
dc.contributor.authorWagner, S
dc.contributor.authorFrancis, GD
dc.contributor.authorClark, SJ
dc.contributor.authorBrown, MA
dc.date.accessioned2017-05-03T14:20:49Z
dc.date.available2017-05-03T14:20:49Z
dc.date.issued2012
dc.date.modified2013-09-09T23:00:58Z
dc.identifier.issn1471-2407
dc.identifier.doi10.1186/1471-2407-12-132
dc.identifier.urihttp://hdl.handle.net/10072/52998
dc.description.abstractBackground Breast cancer outcome, including response to therapy, risk of metastasis and survival, is difficult to predict using currently available methods, highlighting the urgent need for more informative biomarkers. Androgen receptor (AR) has been implicated in breast carcinogenesis however its potential to be an informative biomarker has yet to be fully explored. In this study, AR protein levels were determined in a cohort of 73 Grade III invasive breast ductal adenocarcinomas. Methods The levels of Androgen receptor protein in a cohort of breast tumour samples was determined by immunohistochemistry and the results were compared with clinical characteristics, including survival. The role of defects in the regulation of Androgen receptor gene expression were examined by mutation and methylation screening of the 5' end of the gene, reporter assays of the 5' and 3' end of the AR gene, and searching for miRNAs that may regulate AR gene expression. Results AR was expressed in 56% of tumours and expression was significantly inversely associated with 10-year survival (P = 0.004). An investigation into the mechanisms responsible for the loss of AR expression revealed that hypermethylation of the AR promoter is associated with loss of AR expression in breast cancer cells but not in primary breast tumours. In AR negative breast tumours, mutation screening identified the same mutation (T105A) in the 5'UTR of two AR negative breast cancer patients but not reported in the normal human population. Reporter assay analysis of this mutation however found no evidence for a negative impact on AR 5'UTR activity. The role of miR-124 in regulating AR expression was also investigated, however no evidence for this was found. Conclusion This study highlights the potential for AR expression to be an informative biomarker for breast cancer survival and sets the scene for a more comprehensive investigation of the molecular basis of this phenomenon.
dc.description.peerreviewedYes
dc.description.publicationstatusYes
dc.format.extent519211 bytes
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoeng
dc.publisherBioMed Central
dc.publisher.placeUnited Kingdom
dc.relation.ispartofstudentpublicationN
dc.relation.ispartofpagefrom132-1
dc.relation.ispartofpageto132-10
dc.relation.ispartofjournalBMC Cancer
dc.relation.ispartofvolume12
dc.rights.retentionY
dc.subject.fieldofresearchOncology and carcinogenesis
dc.subject.fieldofresearchcode3211
dc.titleAndrogen receptor expression predicts breast cancer survival: the role of genetic and epigenetic events
dc.typeJournal article
dc.type.descriptionC1 - Articles
dc.type.codeC - Journal Articles
dcterms.licensehttp://creativecommons.org/licenses/by/2.0
gro.description.notepublicPage numbers are not for citation purposes. Instead, this article has the unique article number of 132.
gro.rights.copyright© 2012 Naderi et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
gro.date.issued2012
gro.hasfulltextFull Text
gro.griffith.authorFrancis, Glenn D.


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