Salivary duct carcinomas can be classified into luminal androgen receptor‐positive, HER2 and basal‐like phenotypes*
Adult
Male
Receptor, ErbB-2
03 medical and health sciences
0302 clinical medicine
616
Biomarkers, Tumor
Humans
Salivary Ducts
In Situ Hybridization
Aged
Oligonucleotide Array Sequence Analysis
Aged, 80 and over
Carcinoma
androgen receptor; basal cytokeratins; basal-like phenotype; HER2; molecular subtypes; salivary duct carcinoma
Middle Aged
Salivary Gland Neoplasms
Immunohistochemistry
3. Good health
Carcinoma, Ductal
Phenotype
Receptors, Androgen
Tissue Array Analysis
Female
Carcinoma in Situ
DOI:
10.1111/j.1365-2559.2012.04252.x
Publication Date:
2012-08-09T10:39:13Z
AUTHORS (9)
ABSTRACT
Di Palma S, Simpson R H W, Marchiò C, Skálová A, Ungari M, Sandison A, Whitaker S, Parry S & Reis‐Filho J S
(2012) Histopathology 61, 629–643Salivary duct carcinomas can be classified into luminal androgen receptor‐positive, HER2 and basal‐like phenotypesAims: The aim of this study was to devise a molecular classification for salivary duct carcinomas (SDCs) based on the similarities between SDCs and breast carcinomas and on characteristics of the microarray‐based gene expression profiling‐defined molecular subtypes of breast cancer.Methods and results: Forty‐two pure salivary duct carcinomas, 35 of which contained an in‐situ component as defined by histological review and/or immunohistochemical analysis, were stained with antibodies for oestrogen receptor (ER), progesterone receptor (PR), androgen receptor (AR), human epidermal growth factor receptor 2 (HER2), epidermal growth factor receptor (EGFR) and cytokeratin (CK) 5/6. Based on these markers, tumours were classified into HER2, luminal androgen receptor‐positive, basal‐like, luminal and indeterminate phenotype. Analysis revealed that 16.7%, 69%, 4.8%, 9.5% and 0% were of HER2, luminal androgen receptor‐positive, basal‐like, indeterminate and luminal phenotype, respectively. The in‐situ and invasive components displayed the same molecular subtype in all but one case.Conclusions: Salivary duct carcinomas can be classified into molecular subgroups approximately equivalent to those in the breast. We also report on the existence of a subgroup of bona fide pure salivary duct carcinomas that have a ‘basal‐like’ phenotype. Understanding the phenotypic complexity of SDCs may help to expedite the identification of novel therapeutic targets for these aggressive tumours.
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