The Heterogeneity of Glioblastoma Multiforme and its Applications towards the Dev
The Heterogeneity of Glioblastoma Multiforme and its Applications towards the Dev
批准号:
7983566
负责人:
PAUL S MISCHEL
金额:
$38.12万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-09-03 至 2015-07-31
关键词:
AddressApoptosisAwardBindingBiologicalBiological AssayCCNE1 geneCancer PatientCellsChemicalsClinicClinicalClinical TrialsCompanionsComplementDNADNA amplificationDNA copy numberData SetDiagnosticERBB2 geneEpidermal Growth Factor ReceptorEpigenetic ProcessFoundationsFundingGenesGeneticGenomeGenomicsGlioblastomaGoalsGrantHeterogeneityIn VitroIndividualInformation TheoryIntracellular Signaling ProteinsKnowledgeLibrariesLinkMalignant NeoplasmsMeasurementMeasuresMediatingMethodologyMicrofluidicsModelingMolecularMolecular AnalysisMusMutateMutationOperating RoomsOutcomePTEN geneParaffin EmbeddingPathologyPathway interactionsPatientsPharmaceutical PreparationsPopulationPopulation HeterogeneityPropertyProteinsProteomicsResearch InfrastructureResearch PersonnelResistanceSamplingSequence AnalysisSeriesSignal TransductionSignaling ProteinSolidSolid NeoplasmStromal CellsSurfaceSystems BiologyTP53 geneTechnologyTestingTherapeuticTumorigenicityWorkbasecancer cellcell motilitycell typeclinical applicationclinical careclinically relevantcommercializationdesigneffective therapyexperienceextracellularimprovedlaser capture microdissectionmouse modelnanoneoplastic cellnovel strategiesoncologyphysical scienceprogramsresearch studyresponsesingle cell analysisstatisticstechnology developmenttherapeutic developmenttherapy resistanttooltranslational medicinetumor
中文摘要
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英文摘要
Molecular heterogeneity is central to the development of therapeutic resistance in cancer patients. Current pathology practices are not sufficient for analyzing the molecular and functional properties of heterogeneous populations within a tumor. New approaches are needed for obtaining and using this information to guide more effective treatments that anticipate and suppress therapeutic resistance, and that improve the outcome
for patients with cancer. Project 4 develops platforms combining nano-, chemical and micro-technologies with biological content to facilitate highly multiplexed quantitative molecular and functional measurements of small tumor samples directiy from the operafing room. The technology mix allows us to perform highly multiplexed biological measurements on small enough samples so that we can effectively address the
questions of heterogeneity within solid glioblastoma tumors. The glioblastoma focus of this project permits leveraging the expertise of the investigators and established infrastructure developed during years 1-4 of our CCNE. This infrastructure includes access to meticulously characterized clinical samples, powerful mouse
models, and companion grants obtained over the past few years that pave the way for integration of these technologies into the clinic. The technology pathway within this project begins by leveraging off of the platform of DNA encoded anfibody libraries (DEAL) that was developed under current CCNE funding. We extend this platform to a host of new measurement types for analyzing tumor molecular heterogeneity
resolved to the single cell level. The biological content makes these platforms clinically relevant and adds significant value for commercialization. We aim to develop technologies and approaches that provide information relevant to the clinical care of GBM pafients, but which should also be broadly applicable to other
solid tumor cancers. We have assembled highly cross-disciplinary, interactive team that has several years of experience at working together. Our team bridges from the physical science lab to the oncology clinic.
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