High resolution cell lineage tracking and isolation
High resolution cell lineage tracking and isolation
批准号:
9358785
负责人:
Amy Brock
金额:
$18.83万
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-08-01 至 2020-07-31
关键词:
AcuteAffectArchivesBar CodesBehaviorBiological AssayCell LineageCellsCharacteristicsCommunitiesDataDevelopmentDiagnosisDisease ProgressionDoxorubicinElementsEvolutionFrequenciesGene ExpressionGenerationsGeneticGenomeGenomicsGuide RNAHL60HeterogeneityIndividualLibrariesLongitudinal StudiesMalignant NeoplasmsMammary NeoplasmsMapsMeasurementMethodsMolecularMolecular AnalysisMolecular ProfilingMonitorMutationPhenotypePlasmidsPlayPopulationPopulation HeterogeneityPopulation SizesProliferatingProteomeReporterResolutionSamplingSpecific qualifier valueSystemTechniquesTherapeuticTimeTranscription CoactivatorTumor BiologyTumor Cell LineVariantVincristineanticancer researchcancer cellcancer therapychemotherapeutic agentclinical developmentfitnessinsightinterestleukemiametabolomeneoplastic cellnovelprognosticpromoterresponsescale uptherapy developmenttooltranscriptometranscriptomicstumortumor heterogeneity
中文摘要
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英文摘要
Abstract
Cancer cell populations are marked by significant intratumoral heterogeneity and this
heterogeneity varies over time with disease progression and with response to therapies.
To monitor heterogeneity among large cell populations, barcode sequencing is useful for
quantifying relative lineage frequencies with high resolution. However, current
approaches preclude the simultaneous isolation of a particular lineage of interest. In the
study of cancer and the development of clinical treatments, there are many instances in
which it would be useful to perform subsequent molecular characterization or cellular
functional assays on purified populations of cells exclusively of one specific lineage. A
further challenge is that it is often not possible to identify which lineage is of interest until
a longitudinal study has been completed—for example, comparing the survival and
relative fitness of many cell lineages as they proliferate over many cell generations in a
tumor. Only at the conclusion of a lineage tracing study does it become clear which
specific lineages had a survival advantage. In this proposal we develop a novel lineage
tracing method, Barcode Assisted Ancestral Recall (BAAR), that allows for high-
resolution lineage tracking and subsequent isolation of purified cell lineages for
downstream analysis. Lineage tracing via barcoding is typically a destructive
measurement; with the BAAR system we gain the ability to return to an earlier time point
in the evolutionary trajectory and retrieve selected cells of interest. The ability to
concurrently track clonal fitness dynamics and generate lineage specific genomic and
transcriptomic data over longitudinal studies will give us unprecedented insight into the
behaviors of heterogeneous populations of cancer cells.
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会议论文
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海外基金