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MicroRNAs targeting EGFR signalling pathway in colorectal cancer

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00209805%3A_____%2F13%3A%230000469" target="_blank" >RIV/00209805:_____/13:#0000469 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216224:14740/13:00065617

  • Result on the web

    <a href="http://link.springer.com/article/10.1007%2Fs00432-013-1470-9" target="_blank" >http://link.springer.com/article/10.1007%2Fs00432-013-1470-9</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s00432-013-1470-9" target="_blank" >10.1007/s00432-013-1470-9</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    MicroRNAs targeting EGFR signalling pathway in colorectal cancer

  • Original language description

    MicroRNAs (miRNAs) are short, 18-25-nucleotide long, non-coding single-stranded RNAs, which are capable to regulate gene expression on post-transcriptional level through binding to their target protein-encoding mRNAs. miRNAs regulate individual components of multiple oncogenic pathways. One of them is epidermal growth factor receptor (EGFR) signalling pathway that regulates cell proliferation, differentiation, migration, angiogenesis and apoptosis. All these processes are deregulated in colorectal cancer (CRC). Moreover, EGFR has been validated as the therapeutic target in CRC, and monoclonal antibodies cetuximab and panitumumab are used in the therapy of patients with metastatic CRC. Because of the extensive involvement of miRNAs in the regulation ofEGFR signalling, it seems they could also serve as promising predictive biomarkers to anti-EGFR therapy. In this review, we summarize current knowledge about miRNAs targeting EGFR signalling pathway, their functioning in CRC pathogenesis

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    FD - Oncology and haematology

  • 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)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2013

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Journal of Cancer Research and Clinical Oncology

  • ISSN

    0171-5216

  • e-ISSN

  • Volume of the periodical

    139

  • Issue of the periodical within the volume

    10

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    10

  • Pages from-to

    1615-1624

  • UT code for WoS article

    000324269200002

  • EID of the result in the Scopus database