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    Overexpression of cellular telomerase RNA enhances virus-induced cancer formation (2019)

    Art
    Zeitschriftenartikel / wissenschaftlicher Beitrag
    Autoren
    Kheimar, Ahmed (WE 5)
    Trimpert, Jakob (WE 5)
    Groenke, Nicole (WE 5)
    Kaufer, Benedikt B (WE 5)
    Quelle
    Oncogene
    Bandzählung: 38
    Heftzählung: 10
    Seiten: 1778 – 1786
    ISSN: 1476-5594
    Sprache
    Englisch
    Verweise
    DOI: 10.1038/s41388-018-0544-1
    Pubmed: 30846849
    Kontakt
    Institut für Virologie

    Robert-von-Ostertag-Str. 7-13
    14163 Berlin
    +49 30 838 51833
    virologie@vetmed.fu-berlin.de

    Abstract / Zusammenfassung

    The telomerase RNA subunit (TR) is overexpressed in many tumors; however, the contribution of TR in cancer formation remains elusive. The most frequent clinically diagnosed cancer in the animal kingdom is caused by the highly oncogenic herpesvirus Marek's disease virus (MDV). MDV encodes a TR (vTR) that plays an important role in virus-induced tumorigenesis and shares 88% sequence identity with its cellular homologue. To determine if the cellular TR possesses pro-oncogenic activity, we replaced vTR with the cellular homologue in the virus genome. Insertion of cellular TR resulted in a strong overexpression in virus infected cells, while virus replication was not affected. Strikingly, cellular TR promoted tumor formation as efficient as vTR, while tumorigenesis was severely impaired in the absence of vTR. Our data provide the first evidence that overexpression of cellular TR can contribute to tumor formation in vivo using this natural virus-host model for herpesvirus-induced oncogenesis.