The Role of PI3-Kinase Signaling Pathway in Defining Sensitivity and Resistance
The Role of PI3-Kinase Signaling Pathway in Defining Sensitivity and Resistance
批准号:
7879497
负责人:
JEFFREY A MEYERHARDT
金额:
$39.8万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
关键词:
1-Phosphatidylinositol 3-Kinase1-Phosphatidylinositol 4-KinaseAntibodiesApoptosisArchivesBinding ProteinsBioinformaticsBiopsy SpecimenCancer PatientCancer cell lineCatalytic DomainCell LineCetuximabCharacteristicsClinical ResearchClinical TrialsColon CarcinomaColorectal CancerDana-Farber Cancer InstituteDoseDrug CombinationsEnzymesEpidermal Growth Factor ReceptorEpithelialExcisionGene Expression ProfileGene MutationGenesGeneticGenetic TranscriptionGenomicsGoalsImmunoprecipitationMalignant NeoplasmsMalignant neoplasm of gastrointestinal tractMalignant neoplasm of lungMass Spectrum AnalysisMeasuresModelingMolecular ProfilingMonoclonal AntibodiesMusMutateMutationNude MicePIK3CA geneParaffinParaffin EmbeddingPathway interactionsPatient SelectionPatientsPharmaceutical PreparationsPhase II Clinical TrialsPhosphatidylinositolsPhosphotransferasesProteinsReceptor Protein-Tyrosine KinasesRegulationReproduction sporesResistanceResourcesRoleSamplingSignal PathwaySignal TransductionSignaling ProteinSpecimenTP53 geneTestingTherapeuticTimeTissuesTumor BankTyrosineWestern BlottingXenograft procedurebasecancer geneticscaspase-3cell growthcomparative genomic hybridizationhumanized monoclonal antibodiesindexinginsightkillingskinase inhibitormetastatic colorectalmolecular markerpreclinical studyreceptorresponsetherapeutic targettumortumor xenograft
中文摘要
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英文摘要
Clinical studies indicate that a humanized monoclonal antibody against the Epidermal Growth Factor
Receptor (EGFR), cetuximab, confers an objective tumor response in a subset of patients with metastatic
colorectal cancer. However, most patients do not respond to cetuximab and therefore receive limited or no
benefit from this drug. Currently, there is no test that can predict if a cancer will respond to cetuximab.
Compelling evidence supports the view that targeting the receptor tyrosine kinases (RTK), particularly those
that engage the Phosphoinositide 3-Kinase (PI3K) signaling pathways, is a highly effective strategy for killing
for cancers. Accordingly, the therapeutic response to anti-RTK therapy has been shown to be modulated
dramatically by the mutational status of key signaling components in the PI3K pathway. The PI3K/Akt
signaling pathway drives many epithelial cancers, and its importance in colorectal cancers is underscored by
the presence of PIK3CA mutations (the gene encoding for PI3K) in 20-30% of these cancers. PI3K can be
activated by multiple different signaling pathways including EGFR, and there is accumulating evidence that
EGFR regulates PI3K via distinct mechanisms in cancers sensitive to anti-EGFR therapies. We propose to
study the PI3K signaling pathway, biochemically and genetically, in colorectal cancers with the translationa)
goal of identifying markers that will predict sensitivity to cetuximab. This will enable the selection of patients
that are most likely to benefit from cetuximab. Additionally, these studies may also reveal additional
therapeutic targets to enhance cetuximab sensitivity. Our specific aims include: (1) Identify the mechanisms
for activating the PI3K/AKT pathway in colorectal cancers; (2) To determine the differences in PI3K
regulation between cetuximab sensitive and resistant colorectal cancers in xenograft tumor models; (3) To
determine if we can use the information discovered in the first two aims to identify markers that will predict
which colorectal cancers will respond to cetuximab.
Brief Summary: Cetuximab, a monoclonal antibody against the Epidermal Growth Factor Receptor, is
commonly used to treat patients with metastatic colorectal cancer. However, not all patients benefit from this
therapy and currently there are no reliable molecular markers to select patients that will benefit. The goal of
this project is to find such markers that can be used to select patients most likely to respond to cetuximab.
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