Administrative Core
行政核心
基本信息
- 批准号:10729274
- 负责人:
- 金额:$ 24.24万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2023
- 资助国家:美国
- 起止时间:2023-09-15 至 2028-08-31
- 项目状态:未结题
- 来源:
- 关键词:AdministratorAdvisory CommitteesBrain NeoplasmsBusinessesCellsCollaborationsCommunicationDataDevelopmentEducation and OutreachEnsureEvaluationGlioblastomaGoalsImmuneImmunologicsImmunosuppressionInstitutionInvadedLeadershipModelingMolecularNeuronsOffice of Administrative ManagementPathway interactionsProgram EvaluationProgress ReportsReproducibilityResearchRunningSamplingSite VisitSolid NeoplasmSourceSystemSystems BiologyWorkdynamical evolutionmeetingsneoplastic cellnovel therapeutic interventionprocess improvementsymposiumtherapy resistanttooltumortumor microenvironmenttumor progressionweb page
项目摘要
ABSTRACT - ADMINISTRATIVE CORE
The overarching framework for this MIT/DFCI Center for Systems Biology of Glioblastoma is to use systems
biology to define the dynamic evolution of the tumor-microenvironment interface, focusing on the development
of symbiotic relationships between tumor cells and neurons and tumor cells and immune cells, with the ultimate
goal of using this systems-level molecular characterization to define novel therapeutic strategies to abrogate
tumor progression and overcome therapeutic resistance in brain tumors. While this CSBC Center is focused on
defining the networks and pathways regulating progression, invasion, and immunosuppression in brain tumors,
these issues are highly relevant for most solid tumors, including some of the most aggressive tumor types. Thus,
we envision this CSBC will serve as a nexus for collaborations focused on this topic, and one of the key functions
of the Administrative Core will be to actively cultivate these collaborations. These activities will extend both to
collaborations between institutions involved in the MIT/DFCI CSBC and collaborations across the U54 and U01
holders within the CSBC network. The central work for this CSBC Center revolves around extensive analysis of
bio-specimens that are created by the Biospecimens Core and shared between Projects 1 and 2. The Analytical
Core provides ultra-deep multi-‘omic characterization of biospecimens and other samples, providing data to both
Projects that can then be modeled within each project and across both projects. This highly integrated analysis
of biospecimens will be actively managed by the Administrative Core to ensure a smooth experimental flow.
Finally, this Core will organize and manage the activities of the Center Advisory Committee, the external advisory
board, and interactions with NCI staff.
摘要 - 行政核心
MIT/DFCI 胶质母细胞瘤系统生物学中心的总体框架是使用系统
生物学定义肿瘤-微环境界面的动态演化,重点关注发展
肿瘤细胞与神经元、肿瘤细胞与免疫细胞之间的共生关系,最终
使用这种系统级分子表征来定义新的治疗策略以消除
该 CSBC 中心专注于肿瘤肿瘤并克服脑肿瘤进展中的治疗耐药性。
定义调节脑肿瘤进展、侵袭和免疫抑制的网络和途径,
这些问题与大多数实体瘤高度相关,包括一些最具侵袭性的肿瘤类型。
我们预计该 CSBC 将成为专注于该主题的合作的纽带,也是关键职能之一
行政核心的任务是积极培育这些合作,这些活动将延伸至两者。
参与 MIT/DFCI CSBC 的机构之间的合作以及 U54 和 U01 之间的合作
该 CSBC 中心的核心工作围绕着对 CSBC 网络内的持有人的广泛分析。
由生物样本核心创建并在项目 1 和 2 之间共享的生物样本。
Core 提供生物样本和其他样本的超深入多组学表征,为两者提供数据
然后可以在每个项目内以及跨两个项目对项目进行建模。
生物样本的数量将由行政核心积极管理,以确保实验流程顺利进行。
最后,该核心将组织和管理中心咨询委员会、外部咨询委员会的活动
董事会以及与 NCI 工作人员的互动。
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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Forest M White其他文献
MIT Open Access
麻省理工学院开放获取
- DOI:
10.1364/oe.18.013516 - 发表时间:
2010-06-21 - 期刊:
- 影响因子:3.8
- 作者:
Jonathan A Cooper;Joshua A. Jadwin;Dongmyung Oh;T. Curran;M. Ogiue‐Ikeda;Lin Jia;Forest M White;K. Machida;Ji Yu;Bruce J Mayer - 通讯作者:
Bruce J Mayer
Dendritic cell-mediated cross presentation of tumor-derived peptides is biased against plasma membrane proteins
树突状细胞介导的肿瘤衍生肽的交叉呈递偏向于质膜蛋白
- DOI:
- 发表时间:
2022 - 期刊:
- 影响因子:10.9
- 作者:
Tim B. Fessenden;Lauren E. Stopfer;Fiona Chatterjee;Julian Zulueta;J. Mesfin;Therese Cordero Dumit;I. Reijers;E. Hoefsmit;C. Blank;Forest M White;S. Spranger - 通讯作者:
S. Spranger
Forest M White的其他文献
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{{ truncateString('Forest M White', 18)}}的其他基金
Project 2: Deciphering the Dynamic Evolution of the Tumor-Immune Interface
项目2:破译肿瘤免疫界面的动态演化
- 批准号:
10729276 - 财政年份:2023
- 资助金额:
$ 24.24万 - 项目类别:
Project 2: Tumor characteristics and their effect on therapeutic distribution and efficacy
项目2:肿瘤特征及其对治疗分布和疗效的影响
- 批准号:
9187651 - 财政年份:2016
- 资助金额:
$ 24.24万 - 项目类别:
FASEB SRC on Protein Kinases, Cellular Plasticity and Signal Rewiring
FASEB SRC 关于蛋白激酶、细胞可塑性和信号重新布线
- 批准号:
8782243 - 财政年份:2014
- 资助金额:
$ 24.24万 - 项目类别:
Quantitative Analysis of Epidermal Growth Factor Receptor Signaling Networks
表皮生长因子受体信号网络的定量分析
- 批准号:
7617710 - 财政年份:2008
- 资助金额:
$ 24.24万 - 项目类别:
Quantitative Analysis of Epidermal Growth Factor Receptor Signaling Networks
表皮生长因子受体信号网络的定量分析
- 批准号:
8066673 - 财政年份:2008
- 资助金额:
$ 24.24万 - 项目类别:
Quantitative Analysis of Epidermal Growth Factor Receptor Signaling Networks
表皮生长因子受体信号网络的定量分析
- 批准号:
7466873 - 财政年份:2008
- 资助金额:
$ 24.24万 - 项目类别: