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ERK and RSK regulate distinct steps of a cellular program that induces transition from multicellular epithelium to single cell phenotype

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388971%3A_____%2F13%3A00422123" target="_blank" >RIV/61388971:_____/13:00422123 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.cellsig.2013.08.024" target="_blank" >http://dx.doi.org/10.1016/j.cellsig.2013.08.024</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.cellsig.2013.08.024" target="_blank" >10.1016/j.cellsig.2013.08.024</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    ERK and RSK regulate distinct steps of a cellular program that induces transition from multicellular epithelium to single cell phenotype

  • Original language description

    The ERR (extracellular signal-regulated kinases) cascade has an evolutionarily conserved three tier architecture consisting of protein kinases Raf, MEK (MAPK/ERK kinase) and ERK Following activation, ERK phosphorylates various cellular elements leading to diverse cellular responses. Downstream of ERK the family of p90 ribosomal 56 kinases (RSKs) has been proven to be an important conveyor of ERK signaling, however, little is known if ERK and RSK coordinate their functions to generate a specific biological response. Here we show that in epithelial cells conditional activation of the ERK pathway causes phenotypic conversion of epithelial cells to autonomously migrating cells, This process involves two sequential steps characterized by loss of apical-basal polarity followed by cell scattering. The activation of ERR, but not RSK, is sufficient for the execution of the first step and it requires calpain mediated remodeling of actin cytoskeleton. Conversely, RSK regulates the successive stag

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    EE - Microbiology, virology

  • OECD FORD branch

Result continuities

  • Project

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

  • Continuities

    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

    Cellular Signalling

  • ISSN

    0898-6568

  • e-ISSN

  • Volume of the periodical

    25

  • Issue of the periodical within the volume

    12

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    9

  • Pages from-to

    2743-2751

  • UT code for WoS article

    000328179800042

  • EID of the result in the Scopus database