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Differences in sialyl‐Tn antigen expression between keratoacanthomas and cutaneous squamous cell carcinomas
Author(s) -
Jensen Petter,
Clausen Ole P. F.,
Bryne Magne
Publication year - 1999
Publication title -
journal of cutaneous pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.597
H-Index - 75
eISSN - 1600-0560
pISSN - 0303-6987
DOI - 10.1111/j.1600-0560.1999.tb01826.x
Subject(s) - keratoacanthoma , antigen , pathology , immunohistochemistry , basal cell , cell , medicine , biology , immunology , genetics
Keratoacanthoma and squamous cell carcinoma are common skin tumors, especially in immunosuppressed transplant recipients, but the distinction between these two types of epidermal neoplasia may be difficult. Sialyl‐Tn (Sia‐GalNAc‐O‐Ser/Thr) is a cell surface carbohydrate associated with hyperplasia in squamous epithelium, and correlated with poor prognosis in several human adenocarcinomas. Twenty‐seven keratoacanthomas and 29 cutaneous squamous cell carcinomas were examined for the expression of sialyl‐Tn and of the Ki67 epilope, the latter a marker for cell proliferation. By immunohistochemistry, basaloid tumor cells at the periphery of tumor nests showed some degree of sialyl‐Tn expression in 16 keratoacanthomas (59%), while only three squamous cell carcinomas (10%) showed sialyl‐Tn‐positive basaloid tumor cells (p<0.001). Keratinized, differentiated tumor cells were more often sialyl‐Tn‐positive in keratoacanthomas (89%) than in squamous cell carcinomas (31%) (p<0.001). A striking sialyl‐Tn‐positivity in the basal cell layer was found in a border zone directly adjacent to most tumors of both types (88 and 88%). By immunohistochemical examination of parallel sections and by double immnnofluorescence, sialyl‐Tn antigen expression was primarily seen in cells that did not express Ki67, although some overlap was present. Keratoacanthomas from transplant recipients did not differ in sialyl‐Tn expression compared to those from non‐immunosuppressed patients. The results indicate that sialyl‐Tn expression is not directly related to cell proliferation, but rather to cellular features of post‐mitotic cells, and that sialyl‐Tn is not associated with a malignant phenotype. Sialyl‐Tn may be linked to tumor regression, as seen in keratoacanthomas.