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去整合素-金属蛋白酶ADAM 10、12和17在基底细胞癌侵袭性外周肿瘤细胞中上调。

The disintegrin-metalloproteinases ADAM 10, 12 and 17 are upregulated in invading peripheral tumor cells of basal cell carcinomas.

作者信息

Oh Shin Taek, Schramme A, Stark A, Tilgen W, Gutwein P, Reichrath J

机构信息

Department of Dermatology, Saarland University Hospital, Homburg/Saar, Germany.

出版信息

J Cutan Pathol. 2009 Apr;36(4):395-401. doi: 10.1111/j.1600-0560.2008.01082.x.

Abstract

BACKGROUND

Members of the a disintegrin and metalloproteinase (ADAM) family are expressed in malignant tumors and participate in the pathogenesis of cancer. However, the presence of ADAM 10, 12, 17 and their role in basal cell carcinoma (BCC) have not been described. The purpose of this study was to investigate expression of ADAM 10, 12 and 17 in BCC.

METHODS

Expression of ADAM 10, 12 and 17 was analyzed by immunohistochemistry in skin tissues obtained from 25 patients with different types of BCC.

RESULTS

Immunoreactivity of ADAM 10, 12 and 17 was increased at the peripheral tumor margin compared with central areas of BCC tumor cell nests. Immunoreactivity of ADAM 10 and 12 was increased in the deep margin of invading tumor cell nests in mixed BCC. Focally increased expression of ADAM 12 was detected in squamous differentiated tumor cells of nodular BCC. In addition, immunoreactivity of ADAM 17 was increased in superficial BCC.

CONCLUSIONS

ADAM 10, 12 and 17 showed different expression pattern in BCC histologic subtypes, indicating their different role in the BCC pathogenesis. Overexpression of ADAM 10, 12 and 17 immunoreactivity in deep invasion area of BCC indicates that these three proteases may play an important role in the locally invasive and highly destructive growth behavior of BCC. Additionally, we suggest that ADAM 17 may play an important role in early development of BCC.

摘要

背景

解整合素金属蛋白酶(ADAM)家族成员在恶性肿瘤中表达,并参与癌症的发病机制。然而,ADAM 10、12、17在基底细胞癌(BCC)中的存在情况及其作用尚未见报道。本研究旨在探讨ADAM 10、12和17在基底细胞癌中的表达情况。

方法

采用免疫组织化学方法分析25例不同类型基底细胞癌患者皮肤组织中ADAM 10、12和17的表达。

结果

与基底细胞癌肿瘤细胞巢的中心区域相比,ADAM 10、12和17的免疫反应性在肿瘤边缘外周增加。在混合性基底细胞癌中,ADAM 10和12的免疫反应性在侵袭性肿瘤细胞巢的深部边缘增加。在结节性基底细胞癌的鳞状分化肿瘤细胞中检测到ADAM 12的局部表达增加。此外,浅表性基底细胞癌中ADAM 17的免疫反应性增加。

结论

ADAM 10、12和17在基底细胞癌组织学亚型中表现出不同的表达模式,表明它们在基底细胞癌发病机制中的作用不同。基底细胞癌深部浸润区域中ADAM 10、12和17免疫反应性的过表达表明这三种蛋白酶可能在基底细胞癌的局部侵袭和高度破坏性生长行为中起重要作用。此外,我们认为ADAM 17可能在基底细胞癌的早期发展中起重要作用。

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