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Cytokine expression and signaling in drug-induced cellular senescence

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388971%3A_____%2F10%3A00333900" target="_blank" >RIV/61388971:_____/10:00333900 - isvavai.cz</a>

  • Alternative codes found

    RIV/68378050:_____/10:00333900

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Cytokine expression and signaling in drug-induced cellular senescence

  • Original language description

    Cellular senescence, the permanent state of cell-cycle arrest, is emerging as an intrinsic barrier against tumorigenesis and a mechanism contributing to organismal ageing. Pathophysiologically relevant part of senescent phenotype is the expression and secretion of several cytokines. In this article we present that premature cellular senescence promoted by senescence-inducing compounds (e.g. bromodeoxyuridine, distamycin A, hydroxyurea, and aphidicoline) in several human tumor cell lines is accompanied by persistent activity of the interferon JAK/STAT signaling pathway and the expression of several interferon-stimulated genes such as MX1, OAS, ISG15, STAT1, PML, IRF1 and IRF7. JAK1/STAT-activating ligands IL-10, IL-20, IL-24, IFNgamma, IFNbeta and IL-6were also expressed by senescent cells, supporting autocrine/paracrine activation of JAK1/STAT. Furthermore, cytokine genes including proinflammatory IL-1, TNF and TGF families were highly expressed.

  • 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)<br>Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2010

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Oncogene

  • ISSN

    0950-9232

  • e-ISSN

  • Volume of the periodical

    29

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    12

  • Pages from-to

  • UT code for WoS article

    000273650000010

  • EID of the result in the Scopus database