grant

Pathology & Genomics

Organization DANA-FARBER CANCER INSTLocation BOSTON, UNITED STATESPosted 1 Aug 2022Deadline 31 Jul 2027
NIHUS FederalResearch GrantFY2025AllelesAllelomorphsAnatomic SitesAnatomic structuresAnatomyAntibodiesAreaAssayBioassayBiochemical PathwayBiochemical ProcessBiologicalBiological AssayBiological MarkersBlood PlasmaBody TissuesCancer BiologyCancer CenterCancersCaringCausalityCell BodyCellsCertificationClinical PathologyClinical TreatmentComplementComplement ProteinsCustomCyclicityDF/HCCDNA mutationDana-Farber Cancer InstituteData BasesDatabasesDetection of Minimal Residual DiseaseDevelopmentDiagnosisDiseaseDisorderEGF ReceptorEGFRERBB ProteinEpidermal Growth Factor ReceptorEpidermal Growth Factor Receptor KinaseEpidermal Growth Factor Receptor Protein-Tyrosine KinaseEpidermal Growth Factor-Urogastrone ReceptorsErlotinibEtiologyExpression ProfilingGefitinibGene Expression MonitoringGene Expression Pattern AnalysisGene Expression ProfilingGeneticGenetic ChangeGenetic defectGenetic mutationGenomicsGenotypeGoalsHER1HistologicHistologicallyHybrid captureHybridization captureImageImmuneImmune infiltratesImmunesImmunofluorescenceImmunofluorescence ImmunologicImmunohistochemistryImmunohistochemistry Cell/TissueImmunohistochemistry Staining MethodImmunologic SubtypingImmunomodulationImmunophenotypingIn SituIndividualInternationalInvestigatorsIonsIressaKnowledgeLaboratoriesLung ParenchymaLung TissueMCF3Malignant CellMalignant NeoplasmsMalignant TumorMalignant Tumor of the LungMalignant neoplasm of lungManualsMassive Parallel SequencingMassively Parallel DNA SequencingMassively Parallel SequencingMeasuresMedicineMetabolic NetworksMicroscopicMolecularMolecular GeneticsMonitorMultiplexed Ion Beam ImagingMutationNGS MethodNGS systemOncogenicPathologistPathologyPatient MonitoringPatient SelectionPatientsPeriodicityPlasmaPlasma SerumProceduresProteinsProtocolProtocols documentationPulmonary CancerPulmonary malignant NeoplasmQuality ControlRNA analysisROS1ROS1 geneReproduction sporesResearchResearch PersonnelResearch ResourcesResearch SpecimenResearchersResourcesReticuloendothelial System, Serum, PlasmaRhythmicitySamplingScanningSelection for TreatmentsSeminalServicesSlideSpecimenSpinal ColumnSpineSporesStructure of parenchyma of lungSupervisionSystemTGF-alpha ReceptorTarcevaTechniquesTechnologyTissue ArraysTissue BanksTissue ChipTissue CollectionTissue MicroarrayTissue SampleTissue repositoryTissuesTranscriptTranscript Expression AnalysesTranscript Expression AnalysisTransforming Growth Factor alpha ReceptorTranslational ResearchTranslational ScienceTumor TissueUrogastrone ReceptorValidationVertebral columnWorkXalkorianalyze gene expressionauto-segmentationautomated image analysisautomated segmentationautomatic segmentationautosegmentationbackbonebio-markersbiologicbiologic markerbiomarkerc-erbB-1c-erbB-1 Proteincancer cellcancer microenvironmentcausationcirculating tumor DNA assaycirculating tumor DNA assessmentcirculating tumor DNA evaluationcirculating tumor DNA monitoringcirculating tumor DNA profilingcirculating tumor DNA screeningcirculating tumor DNA testingclinical interventionclinical therapycomplementationcrizotinibctDNA assayctDNA assessmentctDNA evaluationctDNA monitoringctDNA profilingctDNA screeningctDNA testingcustomsdata basedesigndesigningdetection assaydevelopmentaldisease causationerbB-1erbB-1 Proto-Oncogene ProteinerbBlgene expression analysisgene expression assaygenome mutationhybridization-based captureimagingimmune cell infiltrateimmune modulationimmune regulationimmunologic reactivity controlimmunomodulatoryimmunoregulationimmunoregulatoryimprovedinhibitorinnovateinnovationinnovativelung cancermalignancymolecular pathologynanostringneoplasm/cancernew markernext gen sequencingnext generation sequencingnextgen sequencingnovelnovel biomarkernovel markerprotein biomarkersprotein expressionprotein markersproto-oncogene protein c-erbB-1quality assuranceresponsesample collectionselection of treatmentsequencing platformskillsspatial RNA sequencingspatial gene expression analysisspatial gene expression profilingspatial resolved transcriptome sequencingspatial transcriptome analysisspatial transcriptome profilingspatial transcriptome sequencingspatial transcriptomicsspatially resolved transcriptomicsspatio transcriptomicsspecimen collectionstandard of caretherapy selectiontranscriptional profilingtranscriptomicstranslation researchtranslational investigationtreatment and outcometreatment selectiontrial regimentrial treatmenttumortumor DNAtumor cell DNAtumor microenvironmenttumor-specific DNAv-ROS Avian UR2 Sarcoma Virus Oncogene Homolog 1validations
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Full Description

Project Summary:
The Integrated Pathology and Genomics Core provides state-of-the-art analytic services for lung cancer samples

spanning the full spectrum from initial sample handling and processing, to microscopic analysis by certified

anatomic pathologists, to immunophenotypic analysis, to molecular genetic and genomic analysis. This work

constitutes the backbone of lung cancer management, and enables the diagnosis and proper treatment selection

for patients with lung cancers of all types, and also enables research into cancer biology, etiology, and

management. Our pathology core has supported work that has led to major advances in the understanding of

lung cancer biology, and associated management thereof, including seminal discoveries of the importance of

mutations in EGFR, ALK, ROS1, and MET in lung cancer, the diagnosis and management of which have become

the international standard-of-care in this area of medicine. In the same manner, we intend to continue our work

to advance the understanding and care of lung cancer, by supporting the new projects proposed herein, with a

combination of standard-of-care and innovative new cutting-edge technologies.

In this SPORE proposal, we will support each of the proposed projects with a combination of standard-of-care

clinical pathology services - such as histologic characterization of tumors, immunohistochemical assessment of

protein expression, and massively parallel sequencing of tumor DNA - and innovative new techniques. Among

the innovative new techniques to be deployed for this project are customized allele-specific PCR assays for

individual fusion transcripts to enable ultrasensitive monitoring of cell-free circulating ALK rearrangements in

plasma samples, cyclic immunofluorescence and transcriptomics for simultaneous in situ spatial expression of

multiple proteins and transcripts involved in various biochemical pathways, and multiplexed ion beam imaging

to provide high-order assessment of immune cell infiltrates within and adjacent to cancers.

Grant Number: 5P50CA265826-04
NIH Institute/Center: NIH

Principal Investigator: David Barbie

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