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英文摘要
The overall goal of this U54 application is to create and support a highly multidisciplinary team of expert oncologists, biologists, biochemists, engineers and both theoretical and experimental physicists. This team will form a Physical Science-Oncology Center (PS-OC) at the Massachusetts Institute of Technology for Single-Cell Dynamics in Cancer (SCDC). The overarching goal of this team is to use both theoretical and experimental approaches inspired by Physics and Engineering to attack important problems in cancer biology by developing novel technology and analytical/computational methods to track the dynamics of cancer at the single cell level. Most investigators from our team are affiliated with institutes in the Boston area including MIT, the Whitehead Institute for Biomedical Research, the Broad Institute of MIT and Harvard, Harvard Medical School, Brigham and Women's Hospital, and Boston University. Institutions from several other investigators are located at the West coast including the University of California, San Francisco and Stanford University. One of team members is located at the Hubrecht Institute and University Medical Center Utrecht in the Netherlands. The SCDC PS-OC will be based on close collaborations between investigators originating from three fields: cancer biology, experimental physics/engineering and theoretical/computational physics. In Project 1 single-cell transcript counting will be use to develop quantitative models of stem cell differentiation and reprogramming in healthy tissue and cancer. Project 2 utilizes complementary in silico, in vitro, and in vivo studies to deconvolute Ras signaling networks in T cell lymphoma. Project 3 will explore the coordination of cell growth and division in normal and cancer cells and Project 4 focuses on characterizing the load of driver and passenger mutations in cancer by modeling neoplastic progression and analyzing genomic data. All projects will make extensive of the Single-Cell Transcript Counting Core and the Cell Sorting and Physical Measurement Core. These facilities and all reagents generated by the cores will be made available to other PS-OCs.
期刊论文(17)
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会议论文
DOI: 10.1016/j.gde.2012.01.006
发表时间: 2012-04
期刊: CURRENT OPINION IN GENETICS & DEVELOPMENT
影响因子: 4
作者: [Fudenberg, Geoffrey, Mirny, Leonid A.]
通讯作者: Mirny, Leonid A.
DOI: 10.1038/ncb2581
发表时间: 2012-10
期刊: Nature cell biology
影响因子: 21.3
作者: []
通讯作者:
DOI: 10.1016/j.celrep.2013.12.002
发表时间: 2014-01-16
期刊: Cell reports
影响因子: 8.8
作者: [Semrau S, Crosetto N, Bienko M, Boni M, Bernasconi P, Chiarle R, van Oudenaarden A]
通讯作者: van Oudenaarden A
DOI: 10.1038/bcj.2014.67
发表时间: 2014-10-10
期刊: BLOOD CANCER JOURNAL
影响因子: 12.8
作者: [Barreca, A., Martinengo, C., Annaratone, L., Righi, L., Chiappella, A., Ladetto, M., Demurtas, A., Chiusa, L., Stacchini, A., Crosetto, N., van Oudenaarden, A., Chiarle, R.]
通讯作者: Chiarle, R.
10
    Measuring single-cell water content non invasively and with high precision
    Building microenvironment-containing organoids from patient samples with single-cell precision
    Project 1: Systematic discovery of cell-intrinsic mechanisms of cancer drug resistance
    Administrative Core
    国内基金
    海外基金
    层出镰刀菌氮代谢调控因子AreA 介导伏马菌素 FB1 生物合成的作用机理
    • 批准号:
      2021JJ40433
    • 项目类别:
      省市级项目
    • 资助金额:
      --
    • 批准年份:
      2021
    • 负责人:
      孙磊
    • 依托单位:
    寄主诱导梢腐病菌AreA和CYP51基因沉默增强甘蔗抗病性机制解析
    • 批准号:
      32001603
    • 项目类别:
      青年科学基金项目
    • 资助金额:
      24.0万元
    • 批准年份:
      2020
    • 负责人:
      段真珍
    • 依托单位:
    AREA国际经济模型的移植.改进和应用
    • 批准号:
      18870435
    • 项目类别:
      面上项目
    • 资助金额:
      2.0万元
    • 批准年份:
      1988
    • 负责人:
      史树中
    • 依托单位: