A pharmacodynamic model of Aurora kinase inhibitors in the spindle assembly checkpoint

Hitesh B. Mistry, David E. MacCallum, Robert C. Jackson, Mark A. J. Chaplain, Fordyce A. Davidson

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    Abstract

    Arguably the most dramatic phase in the cell cycle is mitosis, during which replicated chromosomes are sorted into two distinct sets. Aurora kinases are central to the accurate segregation of chromosomes during mitosis. Consequently, they have been selected as possible targets for cancer therapy. Anti-cancer drugs that target Aurora kinases are normally designed to inhibit their function. The complexity of the roles of Aurora kinases and their interaction with respective inhibitors means that it is often very difficult to obtain meaningful links between inhibitor concentration and efficacy using standard methods. To overcome these difficulties, we propose a novel mathematical modelling approach. We present a pharmacodynamic model that is able to encapsulate the key roles of two kinases, Aurora A and B, in the spindle assembly checkpoint. Moreover, the model is capable of qualitatively differentiating between the effects of inhibiting Aurora A, Aurora B and A plus B, respectively, by predicting cell behaviour. Consequently, predictions regarding the qualitative relationship between inhibitors, measurable biomarkers and cell damage can be obtained using this powerful modelling approach.
    Original languageEnglish
    Pages (from-to)249-258
    Number of pages10
    JournalFrontiers in Bioscience
    Volume15
    Issue number1
    DOIs
    Publication statusPublished - 2010

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    Keywords

    • Spindle assembly checkpoint
    • Aurora kinase

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