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Overexpression of γ-tubulin in non-small cell lung cancer

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    SYSNO ASEP0387840
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleOverexpression of γ-tubulin in non-small cell lung cancer
    Author(s) Maounis, N.F. (US)
    Dráberová, Eduarda (UMG-J) RID, ORCID
    Mahera, E. (GR)
    Chorti, M. (GR)
    Caracciolo, V. (US)
    Sulimenko, Tetyana (UMG-J)
    Riga, D. (GR)
    Trakas, N. (GR)
    Emmanouilidou, A. (GR)
    Giordano, A. (US)
    Dráber, Pavel (UMG-J) RID, ORCID
    Katsetos, C.D. (US)
    Source TitleHistology and Histopathology. - : Universidad de Murcia - ISSN 0213-3911
    Roč. 27, č. 9 (2012), s. 1183-1194
    Number of pages12 s.
    Languageeng - English
    CountryES - Spain
    Keywordsgamma-tubulin ; microtubules ; NSCLC
    Subject RIVEB - Genetics ; Molecular Biology
    R&D ProjectsGA204/09/1777 GA ČR - Czech Science Foundation (CSF)
    GAP302/10/1701 GA ČR - Czech Science Foundation (CSF)
    LC545 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    CEZAV0Z50520514 - UMG-J (2005-2011)
    UT WOS000306521400007
    AnnotationWWe and others have previously shown that increased expression and altered compartmentalization of γ-tubulin may contribute to tumorigenesis and tumor progression (J. Cell Physiol. 2009;223:519-529; Cancer Biol. Ther. 2010;9:66-76). Here we have determined by immunohistochemistry the localization and cellular distribution of γ-tubulin in clinical tissue samples from 109 non-small cell lung cancer (NSCLC) cases. The expression and distribution of γ-tubulin protein and transcripts was also determined in the NSCLC tumor cell lines NCI-H460 (HTB-177) and NCI-H69 (HTB-119) by immunocytochemistry, quantitative immunoblotting and reverse transcription quantitative real-time PCR (RT-qPCR). Polyclonal and monoclonal anti-peptide antibodies recognizing epitopes in the C- or N-terminal domains of γ-tubulins and human gene-specific primers for γ-tubulins 1 (TUBG1) and 2 (TUBG2) were used. In non-neoplastic cells of the airway epithelium in situ, γ-tubulin exhibited predominantly apical surface and pericentriolar localizations. In contrast, markedly increased, albeit heterogeneous and variously prominent γ-tubulin immunoreactivity was detected in clinical tumor specimens and in the NCI-H460 and NCI-H69 cell lines, where tumor cells exhibited overlapping multi-punctate and diffuse patterns of localization. Co-expression of γ-tubulin and Ki-67 (MIB-1) was detected in a population of proliferating tumor cells. A statistically significant increase of γ-tubulin expression was found in Stage III compared to lesser stage tumors (p<0.001 v. Stages I/II) regardless of histological subtype or grade. By quantitative immunoblotting NCI-H460 and NCI-H69 cells expressed higher levels of γ-tubulin protein compared to small airway epithelial cells (SAEC). In both tumor cell lines increase in TUBG1 and TUBG2 transcripts was detected by RT-qPCR. Our results reveal for the first time an increased expression of γ-tubulin in lung cancer.
    WorkplaceInstitute of Molecular Genetics
    ContactNikol Škňouřilová, nikol.sknourilova@img.cas.cz, Tel.: 241 063 217
    Year of Publishing2013
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