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Fröhlich, E; Mack, AF; Garbe, C; Klessen, C.
Distribution and colocalization of markers for proliferation, invasion, motility and neoangiogenesis in benign melanocytic naevi and malignant melanomas.
Br J Dermatol. 2005; 153(6):1159-1165
Doi: 10.1111/j.1365-2133.2005.06883.x
Web of Science
PubMed
FullText
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- Führende Autor*innen der Med Uni Graz
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Fröhlich Eleonore
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- Abstract:
- BACKGROUND: Melanomas are heterogeneous tumours, and differentiation from other melanocytic lesions may cause problems. It may be possible that the distribution and/or colocalization pattern of different markers in the lesions can enable a more accurate diagnosis of melanocytic tumours. OBJECTIVES: To test this hypothesis, melanocytic naevi, primary melanomas and metastases were investigated. METHODS: The distribution and colocalization of markers for proliferation, invasion, angiogenesis and motility of the tumour cells were investigated using antibodies directed against actin, cathepsin B (CatB), transforming growth factor-beta, vascular endothelial growth factor (VEGF), proliferating cell nuclear antigen/Ki-67 and basic fibroblast growth factor (FGF-2). In addition, melanoma markers (HMB-45 and Melan-A) and proteins unrelated to melanoma progression [epidermal growth factor (EGF) and cathepsin H] were investigated. RESULTS: Malignant melanomas tended to express more markers of malignancy compared with melanocytic naevi, and the differences were statistically significant for EGF and actin immunoreactivity: melanocytic naevi displayed clear EGF labelling more often (60% vs. 5%) and melanomas showed more intense actin labelling (70% vs. 0%). HMB-45+ cells to a large extent also stained with antibodies to CatB but not to EGF or actin; EGF-, FGF-2- and VEGF-immunoreactive cells were predominantly HMB-45-. Similar combinations were observed in melanocytic naevi and in melanomas. CONCLUSIONS: Labelling with EGF may improve the differential diagnosis of melanocytic neoplasias. However, we did not detect a clear-cut increase of markers of malignancy in melanoma. Cells expressing multiple malignancy markers were also found in some melanocytic naevi; this may confirm the dormant potential of melanocytic naevi for melanoma development.
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Cell Movement -
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Cell Proliferation -
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Diagnosis, Differential -
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Epidermal Growth Factor - metabolism
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Humans - metabolism
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Melanoma - blood supply
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Neoplasm Invasiveness - blood supply
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Neoplasm Proteins - metabolism
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Neovascularization, Pathologic - metabolism
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Nevus, Pigmented - blood supply
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Skin Neoplasms - blood supply
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Tumor Markers, Biological - metabolism
- Find related publications in this database (Keywords)
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actin
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epidermal growth factor
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marker
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melanoma
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naevus
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vascular endothelial growth factor