All Benign and Malignant Apocrine Breast Lesions Over-Express Claudin 1 and 3 and Are Negative for Claudin 4

被引:3
|
作者
Shousha, Sami [1 ,2 ]
Anscombe, Oliver [1 ,2 ]
Mcfarlane, Taneisha [1 ,2 ,3 ]
机构
[1] Charing Cross Hosp, Dept Histopathol, Fulham Palace Rd, London W6 8RF, England
[2] Imperial Coll, Fulham Palace Rd, London W6 8RF, England
[3] Imperial Coll, Royal Sch Mines, London SW7 2AZ, England
关键词
Breast; Apocrine breast carcinoma; Triple negative carcinoma; Claudin; 1; 3; 4; INVASIVE DUCTAL CARCINOMA; CANCER; GRADE; FEATURES;
D O I
10.1007/s12253-019-00662-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Invasive apocrine carcinoma of the breast is an uncommon triple negative tumour that lacks a specific therapeutic target. Apocrine metaplasia of the breast shares common morphological features with apocrine carcinoma, and was previously found to consistently over-express claudin 1 and to lack claudin 4. This study was aimed at finding whether apocrine carcinoma, and other related apocrine breast lesions, have similar claudin profile. The immunohistochemical expression of claudin 1, 3 and 4 was studied in 11 cases of in situ and invasive apocrine breast carcinoma, 7 benign apocrine lesions and 45 consecutive morphologically non-apocrine triple negative breast carcinomas. All cases were also immunostained for Gross Cystic Disease Fluid Protein-15 (GCDFP-15), a marker for apocrine differentiation. Apocrine breast lesions maintained their expression pattern from benign through DCIS to invasive carcinoma; all showing strong expression of claudin 1 and 3 and absence of claudin 4. The same pattern of expression was seen in 2 out of the 45 morphologically non-apocrine tumours, but both showed strong positive staining for GCDFP-15. It is concluded that all benign and malignant apocrine lesions of the breast have a consistent pattern of claudin 1, 3 and 4 expression, suggesting the presence of a specific pathway for the development of invasive apocrine carcinoma. The over-expression of claudin 1 and 3 may have therapeutic implications as targets for managing apocrine cancers.
引用
收藏
页码:1073 / 1078
页数:6
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