中华皮肤科杂志 ›› 2013, Vol. 46 ›› Issue (1): 45-46.

• 研究报道 • 上一篇    下一篇

角蛋白17在增殖性皮肤病中的表达

蒋正强1,满孝勇2,郑敏3   

  1. 1. 浙江省临海市第二人民医院
    2. 浙江大学医学院附属第二医院
    3. 杭州:浙江大学医学院附属第二医院
  • 收稿日期:2012-02-22 修回日期:2012-03-12 出版日期:2013-01-15 发布日期:2013-01-01
  • 通讯作者: 满孝勇 E-mail:manxy@zju.edu.cn

Expression of keratin 17 in proliferative skin diseases

1,Man Xiao-Yong2,Min Zheng   

  • Received:2012-02-22 Revised:2012-03-12 Online:2013-01-15 Published:2013-01-01
  • Contact: Man Xiao-Yong E-mail:manxy@zju.edu.cn

摘要: 目的 探讨角蛋白17(K17)在增殖性皮肤病中的表达和意义。 方法 免疫组化法检测K17在正常皮肤、银屑病、基底细胞癌、鳞状细胞癌、恶性黑素瘤中的表达。结果 正常皮肤基底层、棘层、颗粒层的角质形成细胞胞质K17呈阴性表达,银屑病K17强表达于棘层,在基底层呈弱阳性或阴性表达,角化不全细胞不表达。基底细胞癌的瘤细胞不表达K17,瘤细胞旁的棘细胞层、颗粒层细胞呈阳性表达。高分化鳞癌细胞表达K17,而在低分化鳞癌细胞不表达。K17强烈表达于黑素瘤上方表皮全层,在瘤细胞和黑素细胞中不表达。结论 K17的表达可为某些增殖性皮肤病的鉴别诊断提供病理学依据。

关键词: 皮肤疾病, 角蛋白17

Abstract: JIANG Zheng-qiang*, MAN Xiao-yong, ZHENG Min. *Department of Dermatology, Second People′s Hospital of Linhai, Linhai 317016, Zhejiang, China Corresponding author: MAN Xiao-yong, Email: manxyzju@gmail.com 【Abstract】 Objective To investigate the expression and significance of keratin 17 (K17) in proliferative skin diseases, including psoriasis, basal cell carcinoma (BCC), squamous cell carcinoma (SCC) and malignant melanoma. Methods Tissue specimens were collected from the lesions of 14 patients with severe plaque-type psoriasis, 16 patients with BCC, 16 patients with SCC, 8 patients with malignant melanoma, as well as from the normal skin of 17 patients with trauma. Immunohistochemistry was conducted to detect the expression of K17 in these tissue samples. Results K17 was absent in the cytoplasm of keratinocytes in the basal layer, prickle cell layer or granular layer of the normal skin. There was a strong expression of K17 in the prickle cell layer, but a weak or negative expression of K17 in the basal layer of psoriatic skin, and parakeratotic cells did not express K17. In BCC tissues, K17 was absent in carcinoma cells, but visible in peritumoral cells in the prickle cell layer and granular layer. In SCC tissues, K17 was localized in highly differentiated carcinoma cells, but not in lowly differentiated carcinoma cells. There was a strong expression of K17 throughout the epidermis above the melanoma, but a negative expression in the melanoma cells or melanocytes. Conclusion K17 may serve as a molecular marker for the differential diagnosis of some proliferative skin diseases.