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Mesothelial markers in high-grade breast carcinoma.

AbstractAIMS:
Advances in molecular profiling have subdivided breast carcinomas into distinct subtypes. Basal carcinomas are generally oestrogen receptor (ER)-progesterone receptor (PR)-/human epidermal growth factor receptor 2 (HER2)-, and cytokeratin (CK)5/6+. This profile overlaps with that of mesothelial cells. This study of high-grade breast carcinomas was undertaken to determine the expression of mesothelial markers.
METHODS AND RESULTS:
Immunohistochemistry was performed on 23 basal-like breast carcinomas and 30 high-grade breast carcinomas with variable ER, PR and HER2 expression. The incidence of staining of CK5/6, CK14, calretinin, Wilms' tumour 1 (WT1), thrombomodulin and epithelial membrane antigen was assessed statistically. CK14 staining was more specifically associated with triple-negative tumours than CK5/6. Calretinin positivity was statistically associated with basal-like carcinomas. WT1 and thrombomodulin expression was infrequent and limited to a small number of non-basal carcinomas.
CONCLUSIONS:
There is an overlap between the immunophenotype of mesothelial cells and that of basal-like carcinomas of breast. Positive calretinin and CK5/6 are not specific, and may be seen in both mesothelial cells and basal-like breast carcinomas. Negative ER and PR of basal carcinomas may also bias the observer against a breast origin. However, other negative mesothelial markers, such as WT1 and thrombomodulin, may help point to the correct diagnosis.
AuthorsEdwina E Duhig, Lydia Kalpakos, Ian A Yang, Belinda E Clarke
JournalHistopathology (Histopathology) Vol. 59 Issue 5 Pg. 957-64 (Nov 2011) ISSN: 1365-2559 [Electronic] England
PMID22092407 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2011 Blackwell Publishing Limited.
Chemical References
  • Biomarkers, Tumor
Topics
  • Adult
  • Aged
  • Aged, 80 and over
  • Biomarkers, Tumor (analysis)
  • Breast Neoplasms (chemistry, metabolism, pathology)
  • Carcinoma (chemistry, metabolism, pathology)
  • Epithelium (metabolism)
  • Female
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization
  • Middle Aged
  • Neoplasm Grading

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