Glioblastoma - Molecular Analysis for Clinical Trials
Glioblastoma - Molecular Analysis for Clinical Trials
批准号:
6985320
负责人:
PAUL S MISCHEL
金额:
$34.89万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-12-01 至 2009-11-30
关键词:
SCID mouseastrocytomabioinformaticsbiomarkerbiopsyclinical researchclinical trialsenzyme induction /repressionenzyme therapyepidermal growth factorgrowth factor receptorshigh throughput technologyhuman subjecthuman therapy evaluationkinase inhibitormicroarray technologyneoplasm /cancer therapyphosphatidylinositol 3 kinasephosphorylationprognosiswestern blottings
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Kinase inhibitors have demonstrated great promise for the treatment of some types of cancer, such as leukemia and a few solid tumors. Will kinase inhibitors have a more general role in cancer therapy? Glioblastoma, the most common malignant primary brain tumor of adults and one of the most lethal of all cancers, represents an ideal clinical model to address this question. Chronic PI3K/Akt pathway activation promotes malignant transformation and tumor progression in pre-clinical glioblastoma models, and is commonly detected in glioblastoma patient samples. However, clinical application of PI3K/Akt pathway inhibitors has been severely limited by an inability to determine which patient is most likely to benefit. Because morphologically indistinguishable glioblastomas can have distinct classes of causal oncogene/signaling pathway activation that may render them differentially sensitive to kinase inhibitors, it is crucial to develop methods of detecting pathway activation. Our laboratory has developed a method of analyzing PI3K/Akt pathway activation in routinely processed glioblastoma patient biopsies, which may potentially be used to determine which patients are most likely to benefit from kinase inhibitor therapy (Choe et al., 2003), and we have become a molecular correlates analysis center for a number of ongoing, investigator-initiated multi-center clinical trials of targeted pathway inhibitors. This proposal will provide us with a unique opportunity to determine the impact of chronic PI3K pathway activation on patient survival, to determine whether PI3K pathway activation can be used to select patients for targeted inhibitor therapy, and to develop surrogate molecular markers that can be used to detect pathway inhibition and predict response in patients in molecularly-based clinical trials.
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依托单位:
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资助金额:$12.18万
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依托单位:
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依托单位:
海外基金