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Nanotechnologies for Comprehensive Single Cancer Cell Analysis

Nanotechnologies for Comprehensive Single Cancer Cell Analysis
用于综合单癌细胞分析的纳米技术
批准号:
7983244
负责人:
STEPHEN R QUAKE
金额:
$58.69万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-09-01 至 2015-07-31

项目摘要

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中文摘要
翻译
项目概述:针对表皮生长因子受体的癌症治疗 (EGFR)在肺癌中显示出巨大的潜力;然而,这些药物只在一小部分中有效 病人的数量。此外,肿瘤最初是有反应的,随着时间的推移经常会产生耐药性。尽管它 可以直接测量分子(DNA、RNA、蛋白质)和生物物理(质量、密度、电荷) 大量肿瘤的特征,最近的研究表明广泛的细胞到细胞 可变性以及在估计患者预后时表征这种可变性的重要性。我们假设循环细胞的分子和生物物理特征可以区分对治疗有反应的细胞和耐药的细胞。 在分析从循环或其他体液(例如胸腔积液、腹水)收集的细胞时,通常只有少量细胞可用。为了评估这有限数量的细胞的细胞间异质性,我建议开发和应用定量的、全面的单细胞分析设备来评估dna。 为了预测患者对EGFR靶向治疗的可能反应和监测患者对EGFR靶向治疗的抵抗力,单细胞的基因组(例如,单核苷酸多态、融合、缺失)、RNA表达、蛋白质丰度(细胞表面、细胞内和分泌组丰度)以及生物物理特性。N3.3.1)。我们为我们的综合分析平台的开发、测试和应用提出了两个具体目标(表N3.3.1)。
英文摘要
Project Overview: Cancer therapeutics targeted against the Epidermal Growth Factor Receptor (EGFR) have demonstrated great potential in lung cancer; however, these agents are effective in only a subset of patients. Furthermore, tumors tliat are initially responsive frequently acquire resistance over time. Though it is straightforward to measure molecular (DNA, RNA, protein) and biophysical (mass, density, charge) characteristics of tumors in bulk, recent studies have shown wide cell-tocell variability and the importance of characterizing that variability in estimating patient outcome^^^. We hypothesize that molecular and biophysical characterizations of circulating cells can discriminate cells that are responsive to therapy from those that are resistant. When analyzing cells collected from the circulation, or from other bodily fluids (e.g., pleural effusions, ascites), typically only a small number of cells are available. To asses the cell-to-cell heterogeneity of this limited number of cells, ive propose to develop and to apply quantitative, comprehensive single-cell analysis devices for assessing the DNA genome (e.g., single nucleotide polymorphisms, fusions, deletions), RNA expression, protein abundance (cell surface, intracellular, and secretome abundance), and biophysical properties of single cells for the dual purposes of predicting a patient's likely response to EGFR-targeted therapies and for monitoring a patient's acquisition of resistance to EGFR-targeted therapies (Fig. N3.3.1). We propose two specific aims for the development, testing, and application of our comprehensive analysis platform (Table N3.3.1).
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STEPHEN QUAKE PRT TIME
  • 批准号:
    8362085
  • 项目类别:
  • 资助金额:
    $0.03万
  • 财政年份:
    2011
  • 负责人:
    STEPHEN R QUAKE
  • 依托单位:
Genome Transplant Dynamics: non-invasive sequencing-based diagnosis of rejection
  • 批准号:
    8047524
  • 项目类别:
  • 资助金额:
    $246.39万
  • 财政年份:
    2010
  • 负责人:
    STEPHEN R QUAKE
  • 依托单位:
STEPHEN QUAKE PRT TIME
  • 批准号:
    8169986
  • 项目类别:
  • 资助金额:
    $0.03万
  • 财政年份:
    2010
  • 负责人:
    STEPHEN R QUAKE
  • 依托单位:
Microfluidic Techniques for the Molecular and Functional Analysis of Gene Express
  • 批准号:
    7662667
  • 项目类别:
  • 资助金额:
    $44.58万
  • 财政年份:
    2009
  • 负责人:
    STEPHEN R QUAKE
  • 依托单位:
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