Nestin expression in cutaneous melanomas and melanocytic nevi
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
17448190
DOI
10.1111/j.1600-0560.2006.00627.x
PII: CUP627
Knihovny.cz E-resources
- MeSH
- Immunohistochemistry MeSH
- Humans MeSH
- Melanoma blood supply metabolism MeSH
- Biomarkers, Tumor analysis MeSH
- Skin Neoplasms blood supply metabolism MeSH
- Nestin MeSH
- Neovascularization, Pathologic metabolism MeSH
- Nevus, Pigmented blood supply metabolism MeSH
- Intermediate Filament Proteins biosynthesis MeSH
- Nerve Tissue Proteins biosynthesis MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Biomarkers, Tumor MeSH
- NES protein, human MeSH Browser
- Nestin MeSH
- Intermediate Filament Proteins MeSH
- Nerve Tissue Proteins MeSH
BACKGROUND: Nestin is one of the intermediate filaments that are expressed in proliferating neural progenitor cells during development of the central nervous system (CNS) and peripheral nervous system. Postnatal re-expression of the protein occurs mainly under pathological conditions, including injury and neoplasia. In this study, nestin expression was detected in both benign and malignant melanocytic skin lesions and its diagnostic relevance was then evaluated. METHODS: Altogether 139 bioptic tissue samples consisting of 42 nodular melanomas, 32 superficial spreading melanomas, 12 metastatic melanomas, 10 dysplastic nevi and 43 common melanocytic intradermal and dermoepidermal nevi were analysed using indirect immunohistochemical staining. RESULTS: We demonstrated that nestin immunostaining was significantly increased in melanomas where it correlated with more advanced stages of the disease. CONCLUSION: We conclude that expression of the intermediate filament protein nestin might be an indicator of tumor dedifferentiation and more aggressive behaviour. Furthermore, we suggest that nestin might be a relevant marker of tumorous and non-tumorous angiogenesis.
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