Distinct claudin expression characterizes BRCA1-related breast cancer.

Abstract

AIMS:

Members of the claudin family are involved in cancer progression and are differentially expressed in subtypes of breast cancer. Breast cancers in BRCA1 germ line mutation carriers have distinct clinicopathological characteristics. Biomarkers that discriminate between BRCA1-related and sporadic breast cancer cases are needed to improve early identification of mutation carriers. In this study we evaluated protein expression of five major claudins in BRCA1-related breast cancers in comparison with sporadic controls.

METHODS AND RESULTS:

Forty breast cancers in BRCA1 mutation carriers and 40 age-matched sporadic breast cancers were immunohistochemically stained for claudins 1, 3, 4, 6 and 7. Total intratumoural expression levels were compared to those in the surrounding normal tissue. In addition, subcellular claudin expression was scored. Higher overexpression rates were observed for all five claudins in BRCA1-related breast cancers when compared to sporadic controls. In multivariate analysis, overexpression of claudin 3, 4, and 7 was mainly dependent on ER-status, whereas overexpression of claudin 6 and high membranous expression of claudin 1 were independent of other characteristics.

CONCLUSIONS:

BRCA1-related breast cancers are characterized by frequent overexpression of claudins. Especially claudin 1 and 6 expression may help to discriminate mutation carriers from sporadic breast cancer cases.

• Authors: Marise R Heerma van Voss, Paul J van Diest, Yvonne H C M Smolders, Joost Bart, Elsken van der Wall, Petra van der Groep
• Journal: Histopathology (Histopathology) Vol. 65 Issue 6 Pg. 814-27 (Dec 2014) ISSN: 1365-2559 [Electronic] England
• PMID: 25041042 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: © 2014 John Wiley & Sons Ltd.

Chemical References

• Biomarkers, Tumor
• Claudins

Topics

• Biomarkers, Tumor (analysis)
• Breast Neoplasms (genetics, metabolism, pathology)
• Claudins (analysis, biosynthesis)
• Female
• Genes, BRCA1
• Humans
• Immunohistochemistry
• Mutation