Research Program
研究计划
基本信息
- 批准号:10633093
- 负责人:
- 金额:$ 4.91万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1997
- 资助国家:美国
- 起止时间:1997-08-01 至 2025-03-31
- 项目状态:未结题
- 来源:
- 关键词:AbbreviationsAdverse effectsAnimal ModelAntigen-Presenting CellsAreaBasic ScienceBiologicalBiological ModelsBiological ProcessBudgetsCancer BiologyCancer CenterCancer Center Support GrantCancer ModelCancer VaccinesCell modelChromosomal RearrangementCitiesClinicalCollaborationsComplementComplexComputational ScienceComputational algorithmComputer ModelsComputing MethodologiesConnecticutDNA DamageDNA Repair PathwayDNA Sequence AlterationData SetDevelopmentDirect CostsDisciplineEvolutionExtracellular MatrixFaculty RecruitmentFosteringFoundationsFundingFutureGeneticGenetic EngineeringGenetic ModelsGenetic VariationGenomeGenomic InstabilityGenomicsGoalsGrantHealthImmune checkpoint inhibitorImmunodeficient MouseImmunologicsImmunotherapyInvestigationIsraelKnowledgeLaboratoriesLeadershipMaineMalignant NeoplasmsMediatorMedical centerMedicineMethodsModelingMusMutationNCI Center for Cancer ResearchNamesOncogene ActivationOutputPatientsPediatric HospitalsPeer ReviewPhenotypePropertyProteinsPublicationsRecordsResearchResearch PersonnelResearch Project SummariesResearch SupportResistanceResource DevelopmentResourcesSamplingShapesSouthwest Oncology GroupSystemTechnologyTelomere MaintenanceThe Jackson LaboratoryTravelTumor Suppressor ProteinsTumorigenicityUnited States National Institutes of HealthUniversitiesVisionWorkanticancer researchbehavioral responsebiological systemsbiomarker validationcancer cellcancer genomicscancer therapycandidate markerchemotherapycomputing resourcesdesignfunctional genomicsgenetic resourcegenomic aberrationsin vitro Modelin vivoin vivo Modelinnovationinnovative technologiesmeetingsmembermodel developmentneoplastic cellnew technologynovelpatient derived xenograft modelprecision medicineprecision oncologyprogramsresistance mechanismresponsesingle cell technologytechnological innovationtechnology platformtherapeutic targettherapy resistanttranslational potentialtreatment responsetumor
项目摘要
PROJECT SUMMARY RESEARCH PROGRAM
The overarching goal of the JAX Cancer Center (JAXCC) Research Program, Genetic Models for Precision
Cancer Medicine, is to advance the vision of precision oncology through basic research discoveries with
potential for translational and clinical impact. Members use diverse, multi-scale strategies to deconvolute
complex cancer systems to their principal components and to investigate the drivers of cancer cell complexity,
tumor evolution, and tumor adaptation. Elucidating these fundamental biological processes are key to a
principled, mechanistic understanding of the adverse effects of cancer therapy and of treatment resistance.
During the current funding period we have expanded, and reshaped, the JAXCC into a new cancer research
force with a focus on complex genetics and functional genomics. Research is organized around three
complementary Specific Aims. Aim 1 seeks to develop novel organismal, cellular, and computational models of
cancer, drawing on the JAXCC's longstanding strengths in model development. Aim 2 examines the genomic
instability and genetic complexity of cancer and determines their functional consequences in the cancer cell.
Using advanced computational methods and genomic technologies we will interrogate animal models developed
in Aim 1 as well as patient samples. Aim 3 investigates how key components of a tumor and the host contribute
to cancer biology, examining the cancer cell intrinsic and extrinsic components of a malignant tumor. Results
from studies in Aim 3, integrated with the genetic alterations identified in Aim 2 with models developed in Aim 1,
will allow us to deconvolute the complex interactions of the tumor and host microenvironments. The 53 full
program members of the JAXCC include 33 on the Bar Harbor campus and 20 on the Farmington campus.
Through its emphasis on basic research, unique model development, and technological innovation, the program
leverages funding from multiple NIH ICs in support of cancer-focused research. More recently, we brought our
technologies into the clinical arena through collaborations with SWOG, the Maine Cancer Genomics Initiative,
City of Hope, Beth Israel Deaconess Medical Center, University of Connecticut Health Center, and the
Connecticut Children's Hospital. The program is supported by $10,401,511 direct costs in NCI and other peer-
reviewed cancer-related grants in the last budget year. Over the last grant cycle, CCSG funds have supported
379 publications including 30% intra-programmatic collaborations and 72% with external collaborators. The
efforts of the Co-Program Leaders, Drs. Karolina Palucka and Roel Verhaak, and JAXCC leadership have
fostered interactivity among JAXCC members through regular Research Program meetings, subsidized travel
between campuses, and the JAXCC Annual Retreat. The annual JAXCC Retreat and monthly program meetings
are the primary forums that bring together Cancer Center members from both campuses to develop intra-
programmatic collaborations and to participate in the planning for resource development and faculty recruitment.
项目摘要研究计划
JAX癌症中心(JAXCC)研究计划的总体目标,精确的遗传模型
癌症医学是通过与
潜在的翻译和临床影响。成员使用多样化的多尺度策略来宣传
复杂的癌症系统与其主要成分,并研究癌细胞复杂性的驱动因素,
肿瘤演化和肿瘤适应。阐明这些基本的生物学过程是
原则上对癌症治疗和治疗耐药性的不良影响的机械理解。
在当前的资金期间,我们已经扩展并重塑了JAXCC,将
侧重于复杂遗传学和功能基因组学的力。研究大约是三个
互补的特定目的。 AIM 1试图开发新的生物,细胞和计算模型
癌症,借鉴JAXCC在模型开发方面的长期优势。 AIM 2检查基因组
癌症的不稳定性和遗传复杂性,并确定其在癌细胞中的功能后果。
使用先进的计算方法和基因组技术,我们将询问开发的动物模型
在AIM 1和患者样品中。 AIM 3调查了肿瘤和宿主的关键成分如何贡献
为了癌症生物学,检查恶性肿瘤的癌细胞固有和外在成分。结果
根据AIM 3的研究,与AIM 2中确定的遗传变量整合在一起,与AIM 1中开发的模型,
将使我们能够解散肿瘤和宿主微环境的复杂相互作用。 53满
JAXCC的计划成员在Bar Harbour校园内包括33个,在Farmington校园中包括20名。
通过强调基础研究,独特的模型开发和技术创新,该计划
利用多个NIH IC的资金来支持以癌症为中心的研究。最近,我们带来了我们的
通过与缅因州癌症基因组学计划Swog的合作,进入临床领域的技术,
希望之城,贝丝以色列女执事医疗中心,康涅狄格大学健康中心和
康涅狄格州儿童医院。该计划由NCI和其他同行的10,401,511 $ 10,401,511的直接费用支持
在上一个预算中审查了与癌症相关的补助金。在上一个赠款周期中,CCSG资金支持
379个出版物,包括30%的杂项内合作,以及与外部合作者的72%。这
联合计划领导者的努力,博士。 Karolina Palucka和Roel Verhaak和Jaxcc领导
通过常规的研究计划会议,补贴旅行来促进JAXCC成员之间的互动
在校园之间和JAXCC年度静修处。年度JAXCC务虚会和月度课程会议
是将两个校园的癌症中心成员聚集在一起以发展内部的主要论坛
计划合作,并参与资源开发和教师招聘的计划。
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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Jennifer Jean Trowbridge其他文献
Jennifer Jean Trowbridge的其他文献
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{{ truncateString('Jennifer Jean Trowbridge', 18)}}的其他基金
Discovery of Aging-Associated Mechanisms Causing Expansion and Progression of Clonal Hematopoiesis of Indeterminant Potential (CHIP)
发现导致不确定潜能克隆造血(CHIP)扩张和进展的衰老相关机制
- 批准号:
10645132 - 财政年份:2020
- 资助金额:
$ 4.91万 - 项目类别:
Discovery of Aging-Associated Mechanisms Causing Expansion and Progression of Clonal Hematopoiesis of Indeterminant Potential (CHIP)
发现导致不确定潜能克隆造血(CHIP)扩张和进展的衰老相关机制
- 批准号:
10425388 - 财政年份:2020
- 资助金额:
$ 4.91万 - 项目类别:
Discovery of Aging-Associated Mechanisms Causing Expansion and Progression of Clonal Hematopoiesis of Indeterminant Potential (CHIP)
发现导致不确定潜能克隆造血(CHIP)扩张和进展的衰老相关机制
- 批准号:
10226903 - 财政年份:2020
- 资助金额:
$ 4.91万 - 项目类别:
Developing Effective Approaches to Extend Hematopoietic Healthspan by Targeting Cell-extrinsic and Cell-intrinsic Alterations at Middle Age
通过针对中年细胞外在和细胞内在的改变来开发延长造血健康寿命的有效方法
- 批准号:
10449973 - 财政年份:2018
- 资助金额:
$ 4.91万 - 项目类别:
Developing Effective Approaches to Extend Hematopoietic Healthspan by Targeting Cell-extrinsic and Cell-intrinsic Alterations at Middle Age
通过针对中年细胞外在和细胞内在的改变来开发延长造血健康寿命的有效方法
- 批准号:
10192711 - 财政年份:2018
- 资助金额:
$ 4.91万 - 项目类别:
Developing Effective Approaches to Extend Hematopoietic Healthspan by Targeting Cell-Extrinsic and Cell-Intrinsic Alterations at Middle Age
通过针对中年细胞外在和细胞内在的改变来开发延长造血健康寿命的有效方法
- 批准号:
10771727 - 财政年份:2018
- 资助金额:
$ 4.91万 - 项目类别:
Aging-induced Alterations in the Microenvironment as Drivers of Myeloid Lineage Skewing
衰老引起的微环境变化是骨髓谱系偏斜的驱动因素
- 批准号:
9542466 - 财政年份:2017
- 资助金额:
$ 4.91万 - 项目类别:
(PQB5) Epigenetic Drivers of Hematopoietic Stem Cell Transformation
(PQB5) 造血干细胞转化的表观遗传驱动因素
- 批准号:
8685438 - 财政年份:2014
- 资助金额:
$ 4.91万 - 项目类别:
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