Identification of optimal drug combinations targeting cellular networks: Integrating phospho-proteomics and computational network analysis

Sergio Iadevaia, Yiling Lu, Fabiana C. Morales, Gordon B. Mills, Prahlad T. Ram

    Research output: Contribution to journalArticle

    141 Scopus citations

    Abstract

    Targeted therapeutics hold tremendous promise in inhibiting cancer cell proliferation. However, targeting proteins individually can be compensated for by bypass mechanisms and activation of regulatory loops. Designing optimal therapeutic combinations must therefore take into consideration the complex dynamic networks in the cell. In this study, we analyzed the insulin-like growth factor (IGF-1) signaling network in the MDA-MB231 breast cancer cell line. We used reverse-phase protein array to measure the transient changes in the phosphorylation of proteins after IGF-1 stimulation. We developed a computational procedure that integrated mass action modeling with particle swarm optimization to train the model against the experimental data and infer the unknown model parameters. The trained model was used to predict how targeting individual signaling proteins altered the rest of the network and identify drug combinations that minimally increased phosphorylation of other proteins elsewhere in the network. Experimental testing of the modeling predictions showed that optimal drug combinations inhibited cell signaling and proliferation, whereas nonoptimal combination of inhibitors increased phosphorylation of nontargeted proteins and rescued cells from cell death. The integrative approach described here is useful for generating experimental intervention strategies that could optimize drug combinations and discover novel pharmacologic targets for cancer therapy.

    Original languageEnglish (US)
    Pages (from-to)6704-6714
    Number of pages11
    JournalCancer Research
    Volume70
    Issue number17
    DOIs
    StatePublished - Sep 1 2010

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    ASJC Scopus subject areas

    • Oncology
    • Cancer Research

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