Single Cell Sampling of Signaling Activity in Triple Negative Breast Cancer
Single Cell Sampling of Signaling Activity in Triple Negative Breast Cancer
批准号:
9213355
负责人:
DAVID S. LAWRENCE
金额:
$46.62万
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-02-02 至 2021-01-31
关键词:
AddressAffectAgeAgonistBehaviorBiochemicalBiochemistryBiologyBiomedical EngineeringBreast Cancer PatientBreast Cancer cell lineCancer PatientCell LineCellsChemicalsClinicalCommunitiesCytometryDiseaseDisease OutcomeDisease modelDrug MonitoringDrug effect disorderERBB2 geneEnzymesEpidermal Growth Factor ReceptorExhibitsExposure toFamilyFluorescent ProbesFunctional disorderFutureGuidelinesHeterogeneityIndividualInterdisciplinary StudyLaboratoriesLightMeasuresMembraneMole the mammalOncologistPatient SelectionPatientsPatternPharmaceutical PreparationsPharmacologyPhosphotransferasesProtein DephosphorylationProtein KinaseProtein Kinase InhibitorsProtein Tyrosine KinaseProtein phosphataseReceptor Protein-Tyrosine KinasesReporterResearchResolutionRoleSamplingSignal PathwaySignal TransductionSurgeonTechnologyTissuesanticancer researchbasecancer heterogeneityclinical applicationclinical developmentdesigndisease heterogeneitydrug discoveryeffective therapyindividual patientinhibitor/antagonistkinase inhibitormalignant breast neoplasmmolecular subtypesnew technologyoutcome forecastpre-clinicalprecision medicineprogramsprotein kinase inhibitorpublic health relevancereceptorresponsetherapeutic effectivenessthree dimensional cell culturetriple-negative invasive breast carcinomatumortumor heterogeneity
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Breast cancer is commonly divided into four subtypes based on the presence/absence of three distinct receptors: Luminal A, luminal B, HER2, and triple negative/basal-like. Triple negative breast cancer (TNBC) affects approximately 15% of breast cancer patients and has a poorer prognosis than the other subtypes. A major challenge associated with breast cancer in general and TNBC in particular is the heterogeneity of the disease, both between patients and within individual tumors. This has hampered efforts to develop effective therapies. As pointed out by others "the ability to describe tumors at the resolution of single cells will enhance our ability to determine the best treatment options and to anticipate disease outcome". The proposed multidisciplinary research program seeks to develop and apply a technology that simultaneously assesses the intracellular signaling activity of multiple enzymes at the single cell level in TNBC.
We'll compare and contrast the influence of 2D and 3D cell culture conditions as well as antagonists and agonists on signaling activity. In addition, we'll evaluate the presence of subpopulations exhibiting unique signaling behavior. The ability to define heterogeneous aberrant signaling behavior at the single cell level on a patient-by-patient basis could address what is widely viewed as the single most pressing need in TNBC: the absence of guidelines to manage patients with triple-negative disease.
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海外基金