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Insulin-like growth factors (IGFs) system and tumors

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00669806%3A_____%2F16%3A10335292" target="_blank" >RIV/00669806:_____/16:10335292 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11140/16:10335292

  • Result on the web

    <a href="http://www.cupress.cuni.cz/ink2_stat/dload.jsp?prezMat=74633" target="_blank" >http://www.cupress.cuni.cz/ink2_stat/dload.jsp?prezMat=74633</a>

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Insulin-like growth factors (IGFs) system and tumors

  • Original language description

    The interaction between growth factors and cancer incidence and development has been discussed recently. Insulin-like growth factors (IGF, insulin-like growth factors, formerly named somatomedines) are peptides, that participate on growth regulation, metabolism regulation, cell survival and differentiation. They are regulated by growth hormone (GH). IGFs are synthesized in liver and they occur in other body fluids. IGFBPs occur in different body fluids like serum, amniotic fluid and cerebrospinal fluid. IGFBPs are synthesized in liver. These binding proteins serve as storage of IGFs in intercellular space. Effect of IGF1 and IGF2 on cell is mediated by receptors. Signal transduction follows the successful binding to the receptor via signal intracellular pathway - i.e. cascade of enzymes and its substrates. Based on knowledge of IGF1 and IGF2 effect on cells it is assumed that high IGFs serum levels increase the risk for cancer development. They also stimulate proliferation and risk of malignant transformation. High serum levels of binding proteins IGFBPs, particularly dominant serum binding protein IGFBP3, should decrease the risk and inhibit the cellular growth. It is assumed that malignant transformation of the cells can occur independently from serum levels of IGFs in case of presence of functional IGF1R. Recent clinical studies confirmed that high circulating IGF1 concentrations and low IGFBP3 serum levels are related to increase risk for cancer diseases. Negative correlation between IGFBP3 levels and risk of cancer diseases corresponds to protective role of IGFBP3.

  • 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

    <a href="/en/project/EE2.3.20.0040" target="_blank" >EE2.3.20.0040: Molecular genetics of tumor and cardiovascular diseases</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2016

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Plzeňský lékařský sborník

  • ISSN

    0551-1038

  • e-ISSN

  • Volume of the periodical

    2016

  • Issue of the periodical within the volume

    82

  • Country of publishing house

    CZ - CZECH REPUBLIC

  • Number of pages

    7

  • Pages from-to

    17-23

  • UT code for WoS article

  • EID of the result in the Scopus database