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Protein kinase C isoform expression as a predictor of disease outcome on endocrine therapy in breast cancer
  1. J W Assender1,
  2. J M W Gee2,
  3. I Lewis2,
  4. I O Ellis3,
  5. J F R Robertson4,
  6. R I Nicholson2
  1. 1
    CRUK Institute of Cancer Studies, University of Birmingham, Edgbaston, Birmingham, UK
  2. 2
    Tenovus Centre for Cancer Research, Welsh School of Pharmacy, Cardiff University, Cardiff, UK
  3. 3
    Department of Histopathology, City Hospital, Nottingham, UK
  4. 4
    Professional Unit of Surgery, City Hospital, Nottingham, UK
  1. Dr J Assender, CRUK Institute of Cancer Studies, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK; J.W.Assender{at}bham.ac.uk

Abstract

Background: Although in vitro breast cancer models have demonstrated a role for protein kinase C (PKC) α and δ isoforms in endocrine insensitivity and resistance respectively, there is currently little clinical evidence to support these observations.

Aims: To define the pattern of PKC α and δ expression using breast cancer cell lines, with and without endocrine resistance, and also breast cancer samples, where expression can be correlated with clinicopathological and endocrine therapy outcome data.

Methods: PKC isoform expression was examined in tamoxifen responsive, oestrogen receptor positive (ER+), ER+ acquired tamoxifen resistant (TAM-R) and oestrogen receptor negative (ER) cell lines by western blotting and immunocytochemical analysis. PKC isoform expression was then examined by immunohistochemistry in archival breast cancer specimens from primary breast cancer patients with known clinical outcome in relation to endocrine response and survival on therapy.

Results: ER+ breast cancer cell lines expressed considerable PKC-δ but barely detectable levels of PKC-α, whereas ER cell lines expressed PKC-α but little PKC-δ. ER+ acquired TAM-R cell lines expressed substantial levels of both PKC-α and δ. In clinical samples, high PKC-δ expression correlated to endocrine responsiveness whereas PKC-α expression correlated to ER negativity. PKC-δ was an independent predictor of duration of response to therapy. Patients showing a PKC-δ+/PKC-α phenotype had a six times longer endocrine response than patients with the PKC-δ+/ PKC-α+ phenotype (equating to tamoxifen resistance in vitro).

Conclusions: Levels of PKC-α and δ expression appear to be indicative of response to anti-oestrogen therapy and could be useful in predicting a patient’s suitability for endocrine therapy.

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Footnotes

  • Funding: The Tenovus Cancer Research Charity funded the work. The Wales Office of Research and Development for Health and Social Care provided Ian Lewis’s PhD stipend. Wellcome provided Vacation Studentship funding for Frances Boyns, a summer student who did much of the 1HC work under the direction of JMWG.

  • Competing interests: None declared.

  • Abbreviations:
    AP-1
    activator protein-1 complex
    BSA
    bovine serum albumin
    DAB
    diamino benzidine-tetrahydrochloride
    EGF
    epidermal growth factor
    ER
    oestrogen receptor
    ERK2
    extracellular signal-regulated kinase 2
    HR
    hazard ratio
    MAPK
    mitogen activated protein kinase
    NHS
    normal human serum
    PBS
    phosphate buffered saline
    PKC
    protein kinase C
    TAM-R
    tamoxifen resistant
    TBS
    Tris buffered saline

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