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J Oral Pathol Med ; 42(2): 133-9, 2013 Feb.
Article de Anglais | MEDLINE | ID: mdl-22672247

RÉSUMÉ

BACKGROUND: The product of the Wilms' tumor gene, WT1 protein, is a tumor antigen for various kinds of cancer, and WT1 peptide-based cancer immunotherapy is widely anticipated as a new possibility for cancer treatment. The aim of this study was to investigate the expression of WT1 from quantitative and morphological perspectives in oral squamous cell carcinoma (OSCC), the most widespread malignant neoplasm of the oral cavity. METHODS: Six OSCC cell lines and tissue sections from 29 OSCC patients were analyzed. To detect WT1 expression, reverse transcription-polymerase chain reaction analysis (RT-PCR), real-time PCR, Western blots, and immunofluorescence flow cytometry for WT1 were performed on the cell lines, and immunohistochemistry and fluorescence in situ hybridization (FISH) were performed on the tissue sections. RESULTS: WT1 mRNA was found overexpressed in one of the six OSCC cell lines, with expression levels higher than that seen in human leukemia cell line (K562). Immunohistochemical analysis of tissue sections showed overexpression of WT1 protein in two patients, concentrated mainly in the cytoplasm of the outer one to three cell layers of the cancer nests. This was consistent with the expression of WT1 mRNA observed by FISH. Meanwhile, WT1 was not detected on normal oral epithelium. WT1 protein was detected on actively proliferating cancer nests and even on elongated epithelial ridge where new droplet-cancer-nests were being formed and starting infiltration toward subepithelial layer. CONCLUSIONS: The results suggest that WT1 plays an important role in the pathogenesis of some types of OSCC, particularly in proliferation of the cancer cells.


Sujet(s)
Carcinome épidermoïde/anatomopathologie , Tumeurs de la bouche/anatomopathologie , Protéines WT1/analyse , Adulte , Sujet âgé , Sujet âgé de 80 ans ou plus , Technique de Western , Lignée cellulaire tumorale , Prolifération cellulaire , Séparation cellulaire , Cytoplasme/anatomopathologie , Épithélium/anatomopathologie , Femelle , Cytométrie en flux , Régulation de l'expression des gènes tumoraux/génétique , Humains , Immunohistochimie , Hybridation fluorescente in situ , Mâle , Adulte d'âge moyen , Muqueuse de la bouche/anatomopathologie , Invasion tumorale , Réaction de polymérisation en chaine en temps réel , RT-PCR
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