Immunohistochemical expression of matrix metalloproteinase-2 (MMP-2) in common melanocytic nevi, dysplastic nevi and primary cutaneous malignant melanomas
TURKISH JOURNAL OF PATHOLOGY, vol.22, no.2, pp.82-86, 2006 (ESCI)
- Publication Type: Article / Article
- Volume: 22 Issue: 2
- Publication Date: 2006
- Journal Name: TURKISH JOURNAL OF PATHOLOGY
- Journal Indexes: Emerging Sources Citation Index (ESCI)
- Page Numbers: pp.82-86
- Keywords: Common melanocytic nevus, dysplastic nevus, malignant melanoma, immunohistochemistry, MMP-2
- Dokuz Eylül University Affiliated: Yes
Abstract
MMPs play a significant role in the progression of different types of human tumors as well as malignant melanomas. MMP-2, which is also known as 72-kD type IV collagenase is a member of MMPs. The aim of this immunohistochemical study is to evaluate the role of MMP-2 expression in common melanocytic nevi, dysplastic nevi and primary cutaneous malignant melanomas. Formalin-fixed paraffin-embedded materials from 21 common melanocytic nevi (CMN), 42 dysplastic nevi (DN) and 18 primary cutaneous malignant melanomas (MM) were examined. Standard streptavidin-biotin immunoperoxidase method was used for immunostaining with MMP2 antibody. Both tumoral and stromal cytoplasmic MMP2 expressions in melanocytic lesions were scored semiquantitatively. MMP-2 immunoreactivity was not observed in stromal and/or melanocytic cells in either common melanocytic or dysplastic nevi. Eleven of 18 malignant melanomas expressed MMP-2. Five cases showed positive cytoplasmic staining only in stromal cells, and six cases in both stromal and melanocytic cells. MMP-2 was more commonly expressed at the tumor-stroma interface where significant amount of plasma cells and lymphocytes were observed. MMP-2 expression does not appear to be related to the pathobiology of benign melanocytic lesions such as common melanocytic nevi and dysplastic nevi. On the other hand, MMP-2 expression by the cells in the tumor stroma, particularly by endothelial cells and fibroblasts, may play a significant role in melanoma pathobiology.