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
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DOI - Digital Object Identifier
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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
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Czech description
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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
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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
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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
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UT code for WoS article
000273650000010
EID of the result in the Scopus database
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