Nestin expression in cutaneous melanomas and melanocytic nevi

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 inj...

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Published inJournal of cutaneous pathology Vol. 34; no. 5; pp. 370 - 375
Main Authors Brychtova, Svetlana, Fiuraskova, Michala, Hlobilková, Alice, Brychta, Tomas, Hirnak, Jaroslav
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.05.2007
Blackwell
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Summary: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.
Bibliography:ark:/67375/WNG-MWLJNKL2-W
istex:8072A231CD9F506C17A0E9D2C5D8389FA6CF586F
ArticleID:CUP627
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0303-6987
1600-0560
DOI:10.1111/j.1600-0560.2006.00627.x