Sensor-seq: A genome-wide biological measure of microRNA activity.
Sensor-seq: A genome-wide biological measure of microRNA activity.
批准号:
8739636
负责人:
Brian D Brown
金额:
$32.97万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-09-23 至 2016-08-31
关键词:
AddressAdvanced DevelopmentAffectBehaviorBindingBinding SitesBiologicalBiological AssayBiologyCancer BiologyCell physiologyCellsCollectionComplexDataDevelopmentExperimental ModelsFunctional RNAGene ExpressionGene Expression RegulationGenesGeneticHeterogeneityHumanLearningLibrariesMalignant NeoplasmsMeasuresMediatingMethodologyMicroRNAsMolecular ProfilingNeoplasm MetastasisOncogenicOncolytic virusesOutputPatternPharmaceutical PreparationsPilot ProjectsPlayPopulationPopulation HeterogeneityPost-Transcriptional RegulationRegulationReporterResolutionSafetySamplingScientistSiteSpecificitySuicideT-LymphocyteTechnologyTestingTherapeuticTumor Suppressor ProteinsValidationViralVirusVirus Replicationbasecancer cellcancer initiationcancer stem cellcancer therapycell typeexpression vectorgenome-widegenome-wide analysisimprovedinsightneoplastic cellnew technologynovelnovel strategiespublic health relevancescreeningsensorsuicide vectortherapeutic targettooltumortumor progressiontumorigenesisusabilityvector
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): microRNA (miRNA) are a recently uncovered class of regulatory RNAs which help to regulate gene expression, and control cell function. Over 2,000 human miRNAs have been discovered. Many miRNAs have tumor suppressor or oncogenic functions, and miRNA dysregulation has been shown to play a key role oncogenesis, metastasis, and even chemoresistance. Although much has been learned about miRNA biology, as the number of new miRNA genes have been discovered it has become increasingly challenging to annotate relevant miRNA regulatory networks. A critical limitation has been the lack of high-throughput, biological approaches for genome-wide analysis of miRNA behavior. In this R33 proposal, we will develop and validate a new technology and methodology that can be used to: (1) Measure the activity of each and every miRNA within a cell, at single cell resolution,
and (2) Identify optimal synthetic miRNA binding sites that can be used to improve the targeting of suicide vectors and oncolytic viruses being developed for cancer therapies. Our technology will have major utility for expanding our understanding of cancer biology, for generating tools to study and even track specific cancer cell subsets, such as cancer stem cells, for screening for miRNA modulating drugs, and for developing novel therapies that better target tumor cells for destruction.
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海外基金