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    Antivir Chem Chemother. 2010 Jan 5;20(3):133-42.

    The inhibitor of cyclin-dependent kinases, olomoucine II, exhibits potent antiviral properties.

    Source

    Department of Oncological and Experimental Pathology, Masaryk Memorial Cancer Institute, Brno, Czech Republic.

    Abstract

    BACKGROUND:

    Olomoucine II, the most recent derivative of roscovitine, is an exceptionally potent pharmacological inhibitor of cyclin-dependent kinase activities. Here, we report that olomoucine II is also an effective antiviral agent.

    METHODS:

    Antiviral activities of olomoucine II were tested on a range of human viruses in in vitro assays that evaluated viral growth and replication.

    RESULTS:

    Olomoucine II inhibited replication of a broad range of wild-type human viruses, including herpes simplex virus, human adenovirus type-4 and human cytomegalovirus. Olomoucine II also inhibited replication of vaccinia virus and herpes simplex virus mutants resistant to conventional acyclovir treatment. This report is the first demonstration of a poxvirus being sensitive to a cyclin-dependent kinase inhibitor. The antiviral effects of olomoucine II could be observed at lower concentrations than with roscovitine, although both were short-term. A remarkable observation was that olomoucine II, when used in combination with the DNA polymerase inhibitor cidofovir, was able to almost completely eliminate the spread of infectious adenovirus type-4 progeny from infected cells.

    CONCLUSIONS:

    Our results show that when targeting two complementary antiviral mechanisms, strongly additive effects could be observed.

    PMID:
    20054100
    [PubMed - indexed for MEDLINE]
    PMCID:
    PMC2948526
    Free PMC Article

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