Core B: Functional Phenotyping Core
核心 B:功能表型核心
基本信息
- 批准号:10684103
- 负责人:
- 金额:$ 13.01万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2017
- 资助国家:美国
- 起止时间:2017-09-30 至 2027-08-31
- 项目状态:未结题
- 来源:
- 关键词:Acute Myelocytic LeukemiaAddressArchitectureBiological AssayBiologyCell SeparationCell SurvivalClinicClinicalClinical DataClinical TrialsCollectionCommunicationCommunitiesComplexComputerized Medical RecordConsentCryopreservationDataData AnalysesData CorrelationsData ScientistData SetDedicationsDiagnosisDiseaseDisease ProgressionDrug CombinationsEnsureEvolutionFeedsGoalsImmune signalingInformed ConsentInfrastructureIntrinsic factorMalignant NeoplasmsMetadataMethodsModelingMolecularPatient IsolationPatient-Focused OutcomesPatientsPerformancePharmacotherapyPhenotypePreparationProceduresProcessProtocols documentationQuality ControlRecording of previous eventsResearchResearch PersonnelResource SharingResourcesSamplingSecuritySignal TransductionStandardizationStimulusStructureSystemTherapeuticTranslational ResearchTranslationsVariantWorkacquired drug resistancecell preparationdata acquisitiondata curationdata integrationdata managementdata standardsfunctional genomicsgenomic platformimprovedlarge scale dataleukemiamultidisciplinaryneoplastic cellnovelpressureprogramsquality assurancesuccesstherapy resistanttumortumor microenvironment
项目摘要
PROJECT SUMMARY/ABSTRACT: Core B: Functional Phenotyping Core
In the last 20 years, a number of pivotal new treatments have changed the world of cancer as a disease.
Despite these advances, not a single treatment offers a guaranteed cure to everyone who is diagnosed with this
disease. The overall goal of our leukemia-focused ARTNet Center is to understand, on a mechanistic level, how
tumors evolve and adapt under therapeutic pressure leading to loss of tumor control and ultimately disease
progression. Specifically, this application interrogates the temporal extrinsic and intrinsic factors that influence
tumor evolution and its influence on tumor microenvironment in patients with Acute Myeloid Leukemia (AML). In
order to achieve this goal, we have assembled an exceptional team of leukemia researchers, clinicians and data
scientists that have a long history of working together to bridge basic/mechanistic and translational research in
order to tackle AML biology and how this biology changes upon drug treatments.
The Functional Phenotyping core will support this ARTnet project in the standardization, optimization,
and implementation of state-of-the art advanced molecular and functional assays. Additionally, the FP team will
assume oversite, governance as well as integration and standardization of all data collected from each of these
functional genomic assays used in this ARTNet Center. This is an important and essential part of a well-executed
multiparametric and multidisciplinary project, which will allow for extraction of the most meaningful data that can
be cross-compared and interpreted.
The specific aims of the Functional Phenotyping core are to: 1) Optimize standard operating
procedures and provide oversight for the processing, tracking, and dissemination of biospecimens from
AML patients; 2) Work with all ARTNet leaders and researchers to develop and execute SOPs for
functional genomic platforms to facilitate standardized data acquisition and analysis; 3) Serve as data
stewards with regard to governance, security, storage, management, standards, integration, and
dissemination to support intra- and inter-Center analyses and modeling.
In order to achieve these aims, the Functional Phenotyping core will establish and implement SOP-driven
work flows with well-defined milestones and quality check ins across all stages and assays implemented in this
proposal. Further, the FP Core will focus on quality assurance for all assays and help with communication in the
case that unforeseen troubleshooting is required. Overall, the FP core will serve as a resource for all researchers,
making sure the goals of this application are achieved in successful and timely matter.
项目摘要/摘要:核心 B:功能表型核心
在过去 20 年中,许多关键的新疗法改变了癌症作为一种疾病的世界。
尽管取得了这些进展,但没有一种治疗方法可以保证治愈所有被诊断患有此病的人
疾病。我们专注于白血病的 ARTNet 中心的总体目标是在机制层面上了解如何
肿瘤在治疗压力下进化和适应,导致肿瘤失去控制并最终导致疾病
进展。具体来说,该应用程序询问影响时间的外部和内部因素
急性髓系白血病(AML)患者肿瘤进化及其对肿瘤微环境的影响。在
为了实现这一目标,我们组建了一支由白血病研究人员、临床医生和数据组成的杰出团队
有着悠久合作历史的科学家们在基础/机械和转化研究之间架起桥梁
为了解决 AML 生物学问题以及该生物学如何随药物治疗而变化。
功能表型核心将在标准化、优化、
并实施最先进的先进分子和功能测定。此外,FP 团队将
假设从每个这些收集的所有数据的现场、治理以及集成和标准化
该 ARTNet 中心使用的功能基因组测定。这是良好执行的重要且必不可少的部分
多参数和多学科项目,这将允许提取最有意义的数据
进行交叉比较和解释。
功能表型核心的具体目标是: 1) 优化标准操作
程序并为生物样本的处理、跟踪和传播提供监督
急性髓系白血病患者; 2) 与所有 ARTNet 领导者和研究人员合作,制定和执行 SOP
功能基因组平台,促进标准化数据采集和分析; 3)作为数据
治理、安全、存储、管理、标准、集成和
传播以支持中心内和中心间的分析和建模。
为了实现这些目标,功能表型核心将建立并实施 SOP 驱动的
工作流程具有明确定义的里程碑和跨所有阶段的质量检查以及在此实施的分析
提议。此外,FP 核心将专注于所有检测的质量保证,并帮助在
需要进行不可预见的故障排除的情况。总体而言,FP 核心将作为所有研究人员的资源,
确保成功且及时地实现此应用程序的目标。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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{{ truncateString('Tothu Q Vu', 18)}}的其他基金
Neuronal signal transduction in space and time using single quantum dots
使用单量子点进行空间和时间神经元信号转导
- 批准号:
8241032 - 财政年份:2011
- 资助金额:
$ 13.01万 - 项目类别:
Neuronal signal transduction in space and time using single quantum dots
使用单量子点进行空间和时间神经元信号转导
- 批准号:
8695500 - 财政年份:2011
- 资助金额:
$ 13.01万 - 项目类别:
Neuronal signal transduction in space and time using single quantum dots
使用单量子点进行空间和时间神经元信号转导
- 批准号:
8108911 - 财政年份:2011
- 资助金额:
$ 13.01万 - 项目类别:
Neuronal signal transduction in space and time using single quantum dots
使用单量子点进行空间和时间神经元信号转导
- 批准号:
8494700 - 财政年份:2011
- 资助金额:
$ 13.01万 - 项目类别:
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