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Factor XIIIa-positive dendrocytes and proliferative activity of cutaneous cancers
Authors:Claudine Piérard-Franchimont  Jorge E Arrese  Arjen F Nikkels  Géerald E Piérard  Walid Al-Saleh  Philippe Delvenne
Institution:(1) Department of Dermatopathology, University of Liège, CHU Sart Tilman, B-4000 Liège, Belgium;(2) Department of Pathology, University of Liège, CHU Sart Tilman, B-4000 Liège, Belgium
Abstract:Factor XIIIa-positive dendrocytes present at the periphery and inside epithelial neoplasms are an heterogeneous group of cells. They are subsets of mesenchymal cells, cancer-associated macrophages and antigen-presenting cells. Factor XIIIa, other tissue transglutaminases, agr2-macroglobulin and tumour necrosis factor-agr represent a complex network of mediators influencing tumour progression in the skin. In the present study we searched for the presence of dendrocytes and agr2-macroglobulin deposits inside and in the vicinity of cutaneous carcinomas (90 basal cell carcinomas and 46 squamous cell carcinomas) and malignant melanomas (69 primary and 28 metastatic tumours). We also studied the proliferation of the same neoplasms by Ki-67 immunohistochemistry. Dendrocytes were numerous, abutting on and infiltrating most basal cell carcinomas and thin malignant melanomas. In contrast, they were present in only low numbers or even absent in thick primary malignant melanomas and in their metastases. They appeared unmodified around squamous cell carcinomas compared with the surrounding skin. Extracellular deposits of agr2-macroglobulin were often found in locations where dermal dendrocytes were numerous. No correlation was found between the Ki-67 indices of carcinomas and the density of peritumoral dendrocytes. In contrast, negative relationships were found between the Ki-67 indices and the number of dendrocytes present inside basal cell carcinomas and thin malignant melanomas. This study has yielded circumstantial evidence to link the density of factor XIIIa-positive dendritic cells and a low proliferative rate of neoplastic cells in basal cell carcinomas and malignant melanomas.
Keywords:Carcinoma  Cell proliferation  Malignant melanoma  Macrophage  Dendrocyte
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