4.7 Article

Increased claudin-4 expression is associated with poor prognosis and high tumour grade in breast cancer

期刊

INTERNATIONAL JOURNAL OF CANCER
卷 124, 期 9, 页码 2088-2097

出版社

WILEY
DOI: 10.1002/ijc.24159

关键词

breast cancers; tissue microarrays; prognostic biomarkers; claudin-4; tight junctions

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资金

  1. Enterprise Ireland
  2. Irish Research Council for Science Engineering and Technology
  3. Cancer Research Ireland
  4. Science Foundation Ireland
  5. British Association for Cancer Research
  6. Health Research Board of Ireland
  7. Swedish Cancer Society, Swegene/Wallenberg Consortium North, Gunnar, Arvid and Elisabeth Nilsson Cancer Foundation
  8. Per-Eric and Ulla Schyberg Foundation,
  9. Lund University Research Funds
  10. Malmo University Hospital Research and Cancer Funds
  11. Programme for Third Level Institutions (PRTLI)

向作者/读者索取更多资源

The role of intercellular tight junctions in breast epithelia[ cells is traditionaliy thought to be in maintaining polarity and barrier function. However, claudin-4, a tight junction protein, is overexpressed in breast tumour cells compared to normal epithelial cells, which generally corresponds to a loss in polarity. The aim of this study was to investigate the distribution and potential clinical value of claudin-4 in breast cancer, and to evaluate its usefulness as a prognostic and predictive biomarker. Expression of claudin-4 was initially examined by Western blot analysis in a cohort of 88 breast tumours, and was found to correlate positively with tumour grade and negatively with ER. Claudin-4 expression was then evaluated by immunohistochemistry in a larger cohort of 299 tumours represented on a tissue microarray. Claudin-4 expression correlated positively with tumour grade and Hcr2, and negatively with ER. High claudin-4 expression was also associated with worse breast cancer-specific survival (p = 0.0031), recurrence-free survival (P = 0.025) and overall survival (p = 0.034). Multivariate analysis revealed that claudin-4 independently predicted survival in the entire cohort (HR 1.95; 95%CI 1.01-3.79; p = 0.047) and in the ER positive subgroup treated with adjuvant tamoxifen (FIR 4.34; 95%C1 1.14-16.53; p = 0.032). This relationship between increased claudin-4 expression and adverse outcome was validated at the mRNA level in a DNA microarray dataset of 295 breast tumours. We conclude that high levels of claudin-4 protein are associated with adverse outcome in breast cancer patients, including the subgroup of patients treated with adjuvant tamoxifen. (C) 2008 Wiley-Liss, Inc.

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