Craniopharyngioma: a case report and comparative galectin histochemical analysis
Jazyk angličtina Země Nizozemsko Médium print
Typ dokumentu kazuistiky, srovnávací studie, časopisecké články, práce podpořená grantem
PubMed
12495217
DOI
10.1023/a:1020934329211
Knihovny.cz E-zdroje
- MeSH
- bazocelulární nádory metabolismus patologie MeSH
- buněčná diferenciace fyziologie MeSH
- dospělí MeSH
- epitel metabolismus patologie MeSH
- epitopy MeSH
- fenotyp MeSH
- fluorescenční mikroskopie MeSH
- galektiny metabolismus MeSH
- histocytochemie MeSH
- keratiny metabolismus MeSH
- kraniofaryngeom metabolismus patologie MeSH
- lektiny MeSH
- lidé MeSH
- monoklonální protilátky MeSH
- nádorové biomarkery MeSH
- nádory hypofýzy metabolismus patologie MeSH
- polysacharidy metabolismus MeSH
- spinocelulární karcinom metabolismus patologie MeSH
- vazebná místa MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- epitopy MeSH
- galektiny MeSH
- keratiny MeSH
- lektiny MeSH
- monoklonální protilátky MeSH
- nádorové biomarkery MeSH
- polysacharidy MeSH
Craniopharyngioma is a rare benign tumour originating from Rathke's pouch. This paper reports a tumour case studied with a set of markers defining protein-carbohydrate recognition. Expression of endogenous lectins and their reactive glycoligands is under differentiation-dependent control in many cell types. These parameters can be related to the degree of cell differentiation in tumours. Therefore, the expression patterns of endogenous lectins, namely galectins-1, -3, and -7, in the craniopharyngioma case were determined. Galectins-1 and -3 were also used to reveal glycoconjugates in cells and extracellular matrices, an approach that has heretofore relied largely on plant lectins. The staining pattern of craniopharyngioma is compared with that of two other types of ectodermally derived tumours, namely basal and squamous cell carcinomas. Clusters of polygonal and flattened cells with morphological characteristics of differentiated cells in the craniopharyngioma and the majority of poorly differentiated cells in squamous cell carcinomas were reactive with galectin-3. No binding of this probe was observed in cells of basal cell carcinomas and the majority of craniopharyngioma cells. In view of the lack of accessible binding in the basal layer of normal squamous epithelia where proliferative cells (including stem cells) are located, galectin-3 binding could be used to distinguish basal from suprabasal cells of squamous epithelial cells.
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