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dc.contributor.authorMoi, Line Leonora Hauganen_US
dc.contributor.authorFlågeng, Marianne Haugliden_US
dc.contributor.authorGjerde, Jenniferen_US
dc.contributor.authorMadsen, Andreen_US
dc.contributor.authorRøst, Therese Halvorsenen_US
dc.contributor.authorGudbrandsen, Oddrun Anitaen_US
dc.contributor.authorLien, Ernst Asbjørnen_US
dc.contributor.authorMellgren, Gunnaren_US
dc.date.accessioned2014-11-06T14:17:51Z
dc.date.available2014-11-06T14:17:51Z
dc.date.issued2012-06-15eng
dc.identifier.issn1471-2407
dc.identifier.urihttp://hdl.handle.net/1956/8718
dc.description.abstractBackground: Steroid receptor coactivators (SRCs) may modulate estrogen receptor (ER) activity and the response to endocrine treatment in breast cancer, in part through interaction with growth factor receptor signaling pathways. In the present study the effects of tamoxifen treatment on the expression of SRCs and human epidermal growth factor receptors (HERs) were examined in an animal model of ER positive breast cancer. Methods: Sprague-Dawley rats with DMBA-induced breast cancer were randomized to 14 days of oral tamoxifen 40 mg/kg bodyweight/day or vehicle only (controls). Tumors were measured throughout the study period. Blood samples and tumor tissue were collected at sacrifice and tamoxifen and its main metabolites were quantified using LC-MS/MS. The gene expression in tumor of SRC-1, SRC-2/transcription intermediary factor-2 (TIF-2), SRC-3/amplified in breast cancer 1 (AIB1), ER, HER-1, -2, -3 and HER-4, as well as the transcription factor Ets-2, was measured by real-time RT-PCR. Protein levels were further assessed by Western blotting. Results: Tamoxifen and its main metabolites were detected at high concentrations in serum and accumulated in tumor tissue in up to tenfolds the concentration in serum. Mean tumor volume/rat decreased in the tamoxifen treated group, but continued to increase in controls. The mRNA expression levels of SRC-1 (P=0.035), SRC-2/TIF-2 (P=0.002), HER-2 (P = 0.035) and HER-3 (P = 0.006) were significantly higher in tamoxifen treated tumors compared to controls, and the results were confirmed at the protein level using Western blotting. SRC-3/AIB1 protein was also higher in tamoxifen treated tumors. SRC-1 and SRC-2/TIF-2 mRNA levels were positively correlated with each other and with HER-2 (P≤0.001), and the HER-2 mRNA expression correlated with the levels of the other three HER family members (P<0.05). Furthermore, SRC-3/AIB1 and HER-4 were positively correlated with each other and Ets-2 (P<0.001). Conclusions: The expression of SRCs and HER-2 and -3 is stimulated by tamoxifen treatment in DMBA-induced breast cancer. Stimulation and positive correlation of coactivators and HERs may represent an early response to endocrine treatment. The role of SRCs and HER-2 and -3 should be further studied in order to evaluate their effects on response to long-term tamoxifen treatment.en_US
dc.language.isoengeng
dc.publisherBioMed Centraleng
dc.rightsAttribution CC BYeng
dc.rights.urihttp://creativecommons.org/licenses/by/2.0eng
dc.subjectSRC-1eng
dc.subjectSRC-2/TIF-2eng
dc.subjectSRC-3/AIB1eng
dc.subjectHEReng
dc.subjectHER-2eng
dc.subjectBreast cancereng
dc.subjectTamoxifeneng
dc.titleSteroid receptor coactivators, HER-2 and HER-3 expression is stimulated by tamoxifen treatment in DMBA-induced breast canceren_US
dc.typePeer reviewed
dc.typeJournal article
dc.date.updated2013-08-23T09:16:34Z
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2012 Haugan Moi et al.; licensee BioMed Central Ltd
dc.rights.holderLine L Moi et al.; licensee BioMed Central Ltd.
dc.identifier.doihttps://doi.org/10.1186/1471-2407-12-247
dc.identifier.cristin959475
dc.source.articlenumber247
dc.source.journalBMC Cancer
dc.source.volume12


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