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EGFR signaling in the HGG-02 glioblastoma cell line with an unusual loss of EGFR gene copy

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F14%3A00074892" target="_blank" >RIV/00216224:14310/14:00074892 - isvavai.cz</a>

  • Alternative codes found

    RIV/00209805:_____/14:#0000498

  • Result on the web

    <a href="http://dx.doi.org/10.3892/or.2013.2864" target="_blank" >http://dx.doi.org/10.3892/or.2013.2864</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3892/or.2013.2864" target="_blank" >10.3892/or.2013.2864</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    EGFR signaling in the HGG-02 glioblastoma cell line with an unusual loss of EGFR gene copy

  • Original language description

    Epidermal growth factor receptor (EGFR) gene amplification and the overexpression of EGFR are described as common features of glioblastoma multiforme (GBM). Nevertheless, we previously reported the loss of EGFR gene copy in a GBM specimen from a patientwith an unusually favorable course of the disease, and the HGG-02 cell line with this aberration was successfully derived from this tumor. Here, we present a detailed analysis of changes in gene expression and cell signaling in the HGG-02 cell line; theGM7 reference cell line with a standard EGFR gene copy number derived from a very aggressive GBM was used as a control. We confirmed the downregulation of EGFR expression and signaling in HGG-02 cells using different methods (RTK analysis, gene profilingand RT-PCR). Other changes that may have contributed to the non-aggressive phenotype of the primary tumor were identified, including the downregulated phosphorylation of the Axl and Trk receptors, as well as increased activity of JNK and

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    EB - Genetics and molecular biology

  • OECD FORD branch

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2014

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Oncology Reports

  • ISSN

    1021-335X

  • e-ISSN

  • Volume of the periodical

    31

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    GR - GREECE

  • Number of pages

    8

  • Pages from-to

    480-487

  • UT code for WoS article

    000330788100065

  • EID of the result in the Scopus database