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Microarray analysis of serum mRNA in patients with head and neck squamous cell carcinoma at whole-genome scale

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    SYSNO ASEP0435343
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleMicroarray analysis of serum mRNA in patients with head and neck squamous cell carcinoma at whole-genome scale
    Author(s) Čapková, M. (CZ)
    Šáchová, Jana (UMG-J)
    Strnad, Hynek (UMG-J) RID
    Kolář, Michal (UMG-J) RID, ORCID
    Hroudová, Miluše (UMG-J) RID
    Chovanec, M. (CZ)
    Čada, Z. (CZ)
    Štefl, M. (CZ)
    Valach, J. (CZ)
    Kastner, J. (CZ)
    Smetana, K. Jr. (CZ)
    Plzák, J. (CZ)
    Source TitleBioMed Research International. - : Hindawi - ISSN 2314-6133
    -, April 23 (2014)
    Number of pages10 s.
    Languageeng - English
    CountryUS - United States
    KeywordsMicroarray Analysis ; Head and Neck Squamous Cell Carcinoma ; whole-genome scale
    Subject RIVEB - Genetics ; Molecular Biology
    R&D ProjectsNT13488 GA MZd - Ministry of Health (MZ)
    Institutional supportUMG-J - RVO:68378050
    UT WOS000335235800001
    DOI10.1155/2014/408683
    AnnotationWith the increasing demand for noninvasive approaches in monitoring head and neck cancer, circulating nucleic acids have been shown to be a promising tool. We focused on the global transcriptome of serum samples of head and neck squamous cell carcinoma (HNSCC) patients in comparison with healthy individuals. We compared gene expression patterns of 36 samples. Twenty-four participants including 16 HNSCC patients (from 12 patients we obtained blood samples 1 year posttreatment) and 8 control subjects were recruited. The Illumina HumanWG-6 v3 Expression BeadChip was used to profile and identify the differences in serum mRNA transcriptomes. We found 159 genes to be significantly changed (Storey's P value <0.05) between normal and cancer serum specimens regardless of factors including p53 and B-cell lymphoma family members (Bcl-2, Bcl-XL). In contrast, there was no difference in gene expression between samples obtained before and after surgery in cancer patients. We suggest that microarray analysis of serum cRNA in patients with HNSCC should be suitable for refinement of early stage diagnosis of disease that can be important for development of new personalized strategies in diagnosis and treatment of tumours but is not suitable for monitoring further development of disease.
    WorkplaceInstitute of Molecular Genetics
    ContactNikol Škňouřilová, nikol.sknourilova@img.cas.cz, Tel.: 241 063 217
    Year of Publishing2015
Number of the records: 1  

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