Genome-wide Expression Profiling (with Focus on the Galectin Network) in Tumor, Transition Zone and Normal Tissue of Head and Neck Cancer: Marked Differences Between Individual Patients and the Site of Specimen Origin
Jazyk angličtina Země Řecko Médium print
Typ dokumentu časopisecké články
PubMed
28476793
DOI
10.21873/anticanres.11565
PII: 37/5/2275
Knihovny.cz E-zdroje
- Klíčová slova
- Adhesion, glycosylation, lectin, malignancy, proliferation,
- MeSH
- cytokiny genetika MeSH
- epitel metabolismus MeSH
- galektiny genetika metabolismus MeSH
- genom lidský MeSH
- keratiny genetika metabolismus MeSH
- lidé středního věku MeSH
- lidé MeSH
- nádory orofaryngu genetika metabolismus MeSH
- senioři MeSH
- spinocelulární karcinom genetika metabolismus MeSH
- stanovení celkové genové exprese MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- cytokiny MeSH
- galektiny MeSH
- keratiny MeSH
BACKGROUND/AIM: Expression profiling was performed to delineate and characterize the impact of malignancy by comparing tissues from three sites of head and neck cancer of each patient, also determining interindividual variability. MATERIALS AND METHODS: Genome-wide analysis was carried out covering the expression of 25,832 genes with quantification for each site of seven patients with tonsillar or oropharyngeal squamous cell carcinoma. Immunohistochemical analysis was performed for adhesion/growth-regulatory galectins, three pro-inflammatory chemo- and cytokines and keratins. RESULTS: Up- and down-regulation was found for 281 (tumor vs. normal) and 276 genes (transition zone vs. normal), respectively. The profile of the transition zone had its own features, with similarity to the tumor. Galectins were affected in a network manner, with differential regulation and interindividual variability between patients, also true for keratins and the chemo- and cytokines. CONCLUSION: These results underline special features at each site of specimen origin as well as the importance of analyzing galectins as a network and of defining the expression status of the individual patient prior to reaching clinically relevant conclusions.
BIOCEV 1st Faculty of Medicine Charles University Vestec Czech Republic
Institute of Anatomy 1st Faculty of Medicine Charles University Prague Czech Republic
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