Critical oncogenic mutations in newly diagnosed pediatric diffuse intrinsic pontine glioma.

Jacques Grill, Stephanie Puget, Felipe Andreiuolo, Cathy Philippe, Laura MacConaill, Mark W. Kieran

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    96 Citations (Scopus)

    Abstract

    Diffuse intrinsic pontine gliomas (DIPG) can not be cured with current treatment modalities. Targeted therapy in this disease would benefit from advanced technologies detecting relevant drugable mutations. Twenty patients with classic newly diagnosed DIPG underwent stereotactic biopsies and were analyzed for the presence of 983 different mutations in 115 oncogenes and tumor-suppressor genes using OncoMap, a mass spectrometric method of allele detection. Our results identified oncogenic mutations in TP53 (40%), PI3KCA (15%), and ATM/MPL (5%) while none were identified in a large number of other genes commonly mutated in malignant gliomas. The identification of oncogenic mutations in the PI3K pathway offers the potential of a therapeutic target at initial diagnosis in this devastating disease.

    Original languageEnglish
    Pages (from-to)489-491
    Number of pages3
    JournalPediatric Blood and Cancer
    Volume58
    Issue number4
    DOIs
    Publication statusPublished - 1 Apr 2012

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