课题基金 / 基金详情

Mayo Center for Cell Signaling in Gastroenterology

Mayo Center for Cell Signaling in Gastroenterology
梅奥胃肠病学细胞信号转导中心
批准号:
10630250
负责人:
Nicholas F. LaRusso
金额:
$117.98万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-01 至 2024-06-30

项目摘要

项目成果

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中文摘要
翻译
项目摘要 马约胃肠病学细胞信号传导临床中心(C-SiG)的总体目标是利用 胃肠细胞中的信号通路,以改善消化系统疾病患者的健康。为了做到这一点, C-SiG提供了强大的基础设施,主题平台和职业发展机会, 沿着“发现-翻译-应用”的范式扩大有影响力的调查。我们的研究基地 现在包括68名科学家(增长15%),涉及18个部门和2370万美元(直接成本, 2.5%增长)的消化系统疾病相关的资金。响应成员不断变化的兴趣和科学 进步,我们已经重新排列成三个相互关联的机制研究主题(细胞内 信号传导、细胞间通讯和遗传学/表观遗传学),每一个都与三种疾病交叉。 焦点小组(肝脏病理生物学,肠道神经科学,炎症/转化),一个矩阵, 促进发现和疾病相关调查。我们持续的中心假设是, 消化系统疾病患者护理的进步需要一个促进性的基础设施, 研究细胞机制、途径和治疗方法的多学科科学家之间的相互作用 目标是促进基本发现快速转化为临床试验。我们的总体具体目标是 ㈠通过扩大现有机构的技术和协作能力,促进多学科研究 GI科学家和吸引其他学科的研究人员; ii)确定和培养新的GI研究人员 通过同行评审的试点和可行性(P/F)计划,包括职业发展研讨会,课程, (19/26,73%的P/F接受者获得联邦资助); 专门的设备、技术、方法、试剂和专业知识(光学显微镜,临床, 和基因编辑和表观基因组学核心),不断更新核心菜单,质量保证和 (四)支持健全的项目管理体系, v)促进C-SiG与马约的其他NIDDK中心之间的相互作用(例如, PKD中心)和现有的DDRCC,特别是在中西部(即,中西部DDRCC联盟)。我们的全球 这些努力产生了215份手稿,其中56%是专题内出版物,44%是专题间出版物 (70涉及两名或两名以上成员的百分比)。重要的是,我们在了解疾病方面取得了重大进展, 与信号转导、细胞间通讯和遗传学/表观遗传学相关的发病机制, 识别潜在的疾病修饰靶点。
英文摘要
PROJECT SUMMARY The overall objective of the Mayo Clinic Center for Cell Signaling in Gastroenterology (C-SiG) is to exploit signaling pathways in gastrointestinal cells to improve the health of patients with digestive diseases. To do this, C-SiG provides a robust infrastructure, thematic platforms, and career development opportunities to integrate and amplify impactful investigation along the discovery-translation-application paradigm. Our Research Base now consists of 68 scientists (15% growth) involving 18 departments and $23.7 million (direct costs, 2.5% growth) in digestive disease-related funding. Responding to members' evolving interests and scientific advances, we've re-aligned members into three interconnected Mechanistic Research Themes (intracellular signaling, cell-to-cell communication, and genetics/epigenetics), each intersecting with three Disease Focus Groups (liver pathobiology, enteric neurosciences, inflammation/transformation), a matrix that fosters both discovery and disease relevant investigation. Our ongoing CENTRAL HYPOTHESIS is that advances in care of patients with digestive diseases requires a facilitative infrastructure supporting meaningful interactions among multidisciplinary scientists investigating cellular mechanisms, pathways, and therapeutic targets to enhance rapid translation of basic discoveries into clinical trials. Our OVERALL SPECIFIC AIMS are to: i) Foster multidisciplinary research by expanding technical and collaborative capabilities of established GI scientists and attracting investigators from other disciplines; ii) Identify and nurture new GI investigators via a peer-reviewed Pilot and Feasibility (P/F) Program including career development workshops, curricula, and structured mentorship (19/26, 73% of P/F recipients achieving federal funding); iii) Offer core-based specialized equipment, technologies, methodologies, reagents, and expertise (Optical Microscopy, Clinical, and Gene Editing and Epigenomics Cores), with continuous core menu updates, quality assurance and assessments, and project management oversight in response to member feedback; iv) Support a robust Enrichment Program; and v) Promote interactions between C-SiG with other NIDDK centers at Mayo (e.g., PKD Center) and existing DDRCCs, especially in the Midwest (i.e., Midwest DDRCC Alliance). Our global efforts have resulted in 215 manuscripts, with 56% percent intra- and 44% inter-thematic publications (70% involving two or more members). Importantly, we've made critical advances in understanding disease pathogenesis relevant to signal transduction, cell-to-cell communication and genetics/epigenetics, thereby identifying potential disease modifying targets.
期刊论文(576)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1038/onc.2011.329
发表时间: 2012-03-08
期刊: ONCOGENE
影响因子: 8
作者: [Eppinga, R. D., Krueger, E. W., Weller, S. G., Zhang, L., Cao, H., McNiven, M. A.]
通讯作者: McNiven, M. A.
DOI: 10.3350/cmh.2012.18.4.337
发表时间: 2012-12
期刊: Clinical and molecular hepatology
影响因子: 8.9
作者: [Seo YS, Shah VH]
通讯作者: Shah VH
Notch Signaling Coordinates Progenitor Cell-Mediated Biliary Regeneration Following Partial Hepatectomy.
缺口信号传导部分肝切除术后祖细胞介导的胆汁再生。
DOI: 10.1038/srep22754
发表时间: 2016-03-08
期刊: Scientific reports
影响因子: 4.6
作者: [Lu J, Zhou Y, Hu T, Zhang H, Shen M, Cheng P, Dai W, Wang F, Chen K, Zhang Y, Wang C, Li J, Zheng Y, Yang J, Zhu R, Wang J, Lu W, Zhang H, Wang J, Xia Y, De Assuncao TM, Jalan-Sakrikar N, Huebert RC, Bin Zhou, Guo C]
通讯作者: Guo C
DOI: 10.1016/j.micinf.2011.03.008
发表时间: 2011-08
期刊: Microbes and infection
影响因子: 5.8
作者: [O'Hara SP, Chen XM]
通讯作者: Chen XM
共 379 条
    Midwest DDRCC Alliance Conference (Hosted by the Mayo Clinic DDRCC)
    • 批准号:
      10675868
    • 项目类别:
    • 资助金额:
      $2.2万
    • 财政年份:
      2023
    • 负责人:
      Nicholas F. LaRusso
    • 依托单位:
    The Development of TGR5 Antagonists for the Treatment of Cholangiopathies
    The Development of TGR5 Antagonists for the Treatment of Cholangiopathies
    The Development of TGR5 Antagonists for the Treatment of Cholangiopathies
    海外基金