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dc.contributor.authorBerry, A.
dc.contributor.authorCharles, A.
dc.contributor.authorZeps, N.
dc.contributor.authorCregan, D.
dc.contributor.authorArfuso, Frank
dc.contributor.authorDharmarajan, Arunasalam
dc.date.accessioned2017-01-30T12:13:07Z
dc.date.available2017-01-30T12:13:07Z
dc.date.created2015-02-01T20:00:58Z
dc.date.issued2014
dc.identifier.citationBerry, A. and Charles, A. and Zeps, N. and Cregan, D. and Arfuso, F. and Dharmarajan, A. 2014. Expression Profile of Wnt/β-Catenin Signalling Molecules and the Wnt Antagonist Secreted Frizzled-Related Protein 4 in Apoptosis in Breast Cancer Tissue Micro-Arrays. Journal of Analytical Oncology. 3: pp. 205-212.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/19312
dc.identifier.doi10.6000/1927-7229.2014.03.04.4
dc.description.abstract

Wnt proteins are often up-regulated in cancer. The secreted frizzled-related proteins (sFRPs) can abrogate Wnt signalling and are involved in apoptosis. We investigated the expression of Wnt1, β-Catenin, and an antagonist, sFRP4, as well as apoptosis in breast cancer using tissue micro-arrays (TMAs) comprising 191 tissue cores. Results demonstrated stronger staining intensity for Wnt1 in tumour versus non-tumour samples (p<0.05). Epithelial sFRP4 did not differ between invasive and non-invasive tissue; however, there was increased sFRP4 expression in the blood vessels and lymphocyte cells of tumour compared to non-tumour tissue. These data suggest Wnt involvement in determining the breast cancer phenotype and highlight a potential new role for sFRP4 as a diagnostic/prognostic marker.

dc.publisherLifescience Global
dc.subjectWnt
dc.subjectsecreted frizzled-related protein 4
dc.subjectBreast
dc.subjecttissue micro-arrays
dc.subjectcancer
dc.titleExpression Profile of Wnt/β-Catenin Signalling Molecules and the Wnt Antagonist Secreted Frizzled-Related Protein 4 in Apoptosis in Breast Cancer Tissue Micro-Arrays
dc.typeJournal Article
dcterms.source.volume3
dcterms.source.startPage205
dcterms.source.endPage212
dcterms.source.issn1927-7210
dcterms.source.titleJournal of Analytical Oncology
curtin.note

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curtin.departmentSchool of Biomedical Sciences
curtin.accessStatusOpen access


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