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Bacterial intoxication evokes cellular senescence with persistent DNA damage and cytokine signalling

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    SYSNO ASEP0347149
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleBacterial intoxication evokes cellular senescence with persistent DNA damage and cytokine signalling
    Author(s) Blažková, Hana (UMG-J)
    Krejčíková, Kateřina (UMG-J)
    Moudrý, Pavel (UMG-J)
    Frisan, T. (SE)
    Hodný, Zdeněk (UMG-J) RID
    Bártek, Jiří (UMG-J) RID
    Source TitleJournal of Cellular and Molecular Medicine. - : Wiley - ISSN 1582-1838
    Roč. 14, 1-2 (2009), s. 357-367
    Number of pages11 s.
    Languageeng - English
    CountryGB - United Kingdom
    Keywordscellular senescence ; DNA damage response ; bacterial toxins
    Subject RIVEB - Genetics ; Molecular Biology
    R&D ProjectsIAA500390501 GA AV ČR - Academy of Sciences of the Czech Republic (AV ČR)
    GA204/08/1418 GA ČR - Czech Science Foundation (CSF)
    GA301/08/0353 GA ČR - Czech Science Foundation (CSF)
    CEZAV0Z50520514 - UMG-J (2005-2011)
    UT WOS000275639700031
    DOI10.1111/j.1582-4934.2009.00862.x
    AnnotationCytolethal distending toxins (CDT) are proteins produced and secreted by facultative pathogenic strains of gram-negative bacteria with potentially genotoxic effects. We found both normal and cancer human cells exposed to CDT, surviving the acute phase of intoxication by Haemophilus ducreyi CDT, possess the main hallmarks of cellular senescence including persistently activated DNA damage signalling, expansion of promyelocytic leukaemia nuclear compartment and induced expression of several cytokines (e.g. IL-6, IL-8 and IL-24). We conclude that analogous to oncogenic, oxidative and replicative stresses, bacterial toxins represent another pathophysiological stimulus that induces premature senescence. Thus, the activation of cellular senescence as the anticancer barrier, together with evidence of chromosomal defects reported here, support the emerging genotoxic and potentially oncogenic effects of this group of bacterial toxins, and warrant further research of their role in human disease.
    WorkplaceInstitute of Molecular Genetics
    ContactNikol Škňouřilová, nikol.sknourilova@img.cas.cz, Tel.: 241 063 217
    Year of Publishing2011
Number of the records: 1  

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