Integrated genomic approaches to identify and validate cancer targets
Integrated genomic approaches to identify and validate cancer targets
批准号:
7614367
负责人:
William C. Hahn
金额:
$53.15万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-04-15 至 2011-03-31
关键词:
Atlas of Cancer Mortality in the United StatesBiological AssayBreast Cancer CellCancer ModelCancer cell lineCarcinomaCell ProliferationChromosomal DuplicationClassificationCollectionComplementData SetDevelopmentEpithelialEpithelial CellsEventExhibitsExperimental ModelsFoundationsGene MutationGene TargetingGenesGenomeGenomicsGoalsHumanKnowledgeLaboratoriesLibrariesMalignant - descriptorMalignant NeoplasmsMammary NeoplasmsMammary glandMapsMethodologyMethodsMolecularMutationNormal tissue morphologyOncogenesOpen Reading FramesPathway AnalysisPhenotypeProtein-Protein Interaction MapProteinsRNA InterferenceReagentRecurrenceRelative (related person)Signal PathwaySignal TransductionSingle Nucleotide PolymorphismTechnologyTherapeuticValidationWorkbasecancer genomecell transformationcomparative genomic hybridizationdensitygain of functiongene discoveryloss of functionmalignant breast neoplasmneoplasticnoveloverexpressionprogramsresearch studytherapeutic targettooltumor
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Most human tumors, particularly those derived from epithelial cancers, exhibit global genomic alterations that make it difficult to identify mutations critical for cell transformation and to define the consequences of specific cancer-associated mutations. Recent advances in technologies to identify structural changes in human cancers now make it possible to consider enumerating all of the genetic alterations harbored by a particular tumor. Despite these advances in annotating structural alterations in cancer genomes, identifying the genes targeted by specific amplification or deletion events and deciphering the function of targeted gene mutations remains a major challenge. Indeed, the parallel development of efficient methods to annotate the function of cancer-associated genes is necessary to distill validated cancer targets from this structural description of cancer genomes.
This proposal focuses on the integration of newly developed, high throughput methods to functionally annotate the cancer genome. Specifically, methods to perform large scale loss-of function, gain-of-function, and protein-protein network analyses will be combined in a novel integrated program to identify and validate functionally important cancer genes. Specifically, these studies build upon prior work by our laboratories to develop and implement genome scale RNA interference libraries, complete collections of human open reading frames (ORFs) and comprehensive protein-protein interaction maps. Although the basic tools required to perform large-scale studies are now available, the integration of such whole genome approaches represents an entirely new endeavor that requires the further development of these nascent technologies, the fabrication of comprehensive reagents and the creation of new ways to connect these datasets to achieve a scale beyond what has been previously performed. As such, the overarching goals of this R33 application is to apply these technologies in an integrated manner while simultaneously identifying and validating genes of particular promise for therapeutic targeting. The long-term goal of these studies is to provide a foundation for the expansion of these efforts at genome scale.
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财政年份:2017
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Systematic identification of oncogenic KRAS synthetic lethal interactions
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财政年份:2015
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依托单位:
The Dana-Farber Cancer Institute Cancer Target Discovery and Development Center
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批准号:9362809
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资助金额:$102.74万
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财政年份:2013
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依托单位:
The Dana-Farber Cancer Institute Cancer Target Discovery and Development Center
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批准号:9979771
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资助金额:$100.76万
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财政年份:2013
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依托单位:
Identification of TBK1 inhibitors in KRAS-dependent lung cancer
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批准号:8237125
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资助金额:$42.96万
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财政年份:2012
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依托单位:
Discovering modulators of PAX8 for targeting ovarian cancer
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批准号:8548405
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财政年份:2012
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依托单位:
Discovering modulators of PAX8 for targeting ovarian cancer
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批准号:8403869
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财政年份:2012
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依托单位:
Project 2: Identification of combination therapy for KRAS-driven lung cancers.
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批准号:10231099
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资助金额:$28.86万
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财政年份:2012
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依托单位:
Gene Function Manipulation Core
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批准号:8233036
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财政年份:2011
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依托单位:
Druggable Genetic Lesions in Pediatric Astrocytoma
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批准号:8044508
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依托单位:
Interactions of the SV40 Small t Antigen and PP2A in Human Cell Transformation
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依托单位:
Investigations on the role of the CDK8 oncogene in colon cancer
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依托单位:
Investigations on the role of the CDK8 oncogene in colon cancer
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依托单位:
Investigations on the role of the CDK8 oncogene in colon cancer
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依托单位:
海外基金