Expression of stromelysin 3 in keratoacanthoma and squamous cell carcinoma

被引:27
作者
Asch, PH
Basset, P
Roos, M
Grosshans, E
Bellocq, JP
Cribier, B
机构
[1] Hop Univ, Dermatol Clin, F-67091 Strasbourg, France
[2] Inst Genet & Biol Mol & Cellulaire, Illkirch, France
[3] Fac Med Strasbourg, Unite Biostat, Strasbourg, France
[4] Serv Anat Pathol Gen, Strasbourg, France
关键词
squamous cell carcinoma; keratoacanthoma; metalloproteinase; stromelysin; 3; immunohistochemistry;
D O I
10.1097/00000372-199904000-00006
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 [皮肤病与性病学];
摘要
Stromelysin 3 (ST3) is a member of the metalloproteinase family, which is expressed in the skin during wound healing and in the stroma of basal cell carcinoma. A high level of expression of ST3 has been observed in carcinomas of poor prognosis. In benign tumors, though, ST3 is not expressed or is at a low level. We have immunohistochemically studied the expression of ST3 in 89 randomly selected cases of squamous cell carcinomas (SCCs), 104 of keratoacanthomas (KA), and 23 cases of metastatic SCC. Stromelysin 3 was expressed only by fibroblasts surrounding the tumors and not by epithelial cells. The proportion of tumors positively stained was 22% of KA, 47% of randomly selected SCC, and 70% of metastatic SCC. In areas of poorly demarcated neoplastic cells, a reinforcement of the staining was observed in the stroma. The intensity and dispersion of staining were used to determine the level of expression. There were significantly more SCC in the groups of high expression levels, and both parameters were significantly higher in SCC than in KA. Expression of ST3 in benign tumors is unusual. Its expression in the the stroma of keratoacanthomas can be related to the high tissue remodeling activity observed in these tumors. It also could be interpreted as in favor of the neoplastic nature of KA. Nevertheless, the level of expression was higher in SCC than in KA and seemed to be related to the prognosis of these tumors. These results correlate well with those obtained in boast cancers and in noncutaneous SCC.
引用
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页码:146 / 150
页数:5
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