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    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

    213311_143024_2014_Breast_cancerTMAs.pdf (3.759Mb)
    Access Status
    Open access
    Authors
    Berry, A.
    Charles, A.
    Zeps, N.
    Cregan, D.
    Arfuso, Frank
    Dharmarajan, Arunasalam
    Date
    2014
    Type
    Journal Article
    
    Metadata
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    Citation
    Berry, 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.
    Source Title
    Journal of Analytical Oncology
    DOI
    10.6000/1927-7229.2014.03.04.4
    ISSN
    1927-7210
    School
    School of Biomedical Sciences
    Remarks

    The link to the journal can be found in the Related links field

    URI
    http://hdl.handle.net/20.500.11937/19312
    Collection
    • Curtin Research Publications
    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.

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