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中文摘要
翻译
癌症的复杂性,特别是在转移的建立和生长方面,阻碍了对肿瘤细胞与非转化细胞的不同之处的全面了解。癌细胞在体内迁移并存活。周围血流是启动转移灶的特定血管部位的家园,并对局部间质进行重新编程并诱导新血管生成,从而允许转移灶的建立和生长。为了解开这种复杂性并确定新的药理靶点来抑制肿瘤转移的开始和生长,我们将利用我们在康奈尔大学复杂的微米和纳米制造方面的显著优势。这种方法将使3D结构的形成具有精确控制和“可调”的尺寸,以概括和定量测试转移肿瘤微环境中的物理化学决定因素。该中心的物理科学研究人员汇集了小规模材料加工、物理测量和建模方面最先进的方法方面的杰出专业知识。在这项工作中,以物理科学和工程为基础的研究人员在纳米生物技术和使用方法在细胞和分子水平上探索生命过程方面处于世界领先地位。在这一应用中,这些主要为物理科学实验开发的方法将被应用于癌症的研究,重点是剖析通过与组织间质和新生肿瘤血管系统的相互作用来调节循环中的肿瘤细胞迁移、黏附和建立转移灶的分子机制。该团队与威尔医学院癌症中心和布法罗大学的领先癌症研究人员合作,将使人们对肿瘤细胞(包括患者来源的循环肿瘤细胞)及其与特定微环境的相互作用有一个新的基本了解。这些研究将使用无偏见的基因和途径发现方法来促进对癌症转移新干预措施的可行途径的预测,而不是关注用于干预的候选基因。将强调对初级研究人员和教职员工进行跨物理科学和癌症生物学学科的交叉培训,以培养新一代科学家探索癌症的科学基础。向物理科学肿瘤学中心的研究人员提供新的核心设施,包括选定的细胞表观基因组分析和新开发的微米和纳米制造方法,以丰富合作并在整个网络中传播技术进步。通过这种方法,这项研究的影响应该比普通的个人调查项目更广泛地感受到。
英文摘要
The complexity of cancer, particularly in the establishment and growth of metastases, has hampered a comprehensive understanding of how tumor cells differ from their non-transformed counterparts. Cancer cells migrate and survive in. the peripheral bloodstream, home to specific vascular sites to initiate metastatic foci, and reprogram local stroma and induce neoangiogenesis to, permit establishment and growth of metastatic lesions. To deconvolute this complexity and to identify new pharmacological targets to inhibit metastasis initiation and growth, we will draw on our significant strengths in sophisticated micro and nanofabrication at Cornell University. This approach will enable the formation of 3D structures with precisely controlled and "tunable" dimensions to recapitulate and quantitatively test physicochemical determinants in the metastatic tumor microenvironment. The physical science researchers in this center bring together outstanding expertise in the most modem approaches for small scale materials processing, physical measurements and modeling. The physical science and engineering based researchers in this effort are among he world's leaders in nanobiotechnology and in the use of methods to probe life processes at the cellular and molecular level. In this application, these approaches, developed primarily for physical science experimentation, will be adapted and brought to bear on the study of cancer, with an emphasis on dissecting the molecular mechanisms that regulate circulating tumor cell migration, adhesion and the establishment of metastatic foci via interactions with tissue stroma and the nascent tumor vasculature. Working together with leading cancer investigators at Weill Medical College Cancer Center and the University of Buffalo, this team will inform a new fundamental level of understanding of tumor cells, including patient-derived circulating tumor cells, and their interaction with defined microenvironments. Rather than focusing on candidate genes for intervention, these studies will use unbiased gene and pathway discovery approaches to facilitate prediction of viable pathways for novel interventions in cancer metastasis. Cross-training of junior investigators and faculty across physical science and cancer biology disciplines will be emphasized, to educate a new generation of scientist to explore the scientific basis of cancer. New core facilities, including selected cell epigenomic analysis, and newly developed methods in micro and nanofabrication be made available to researchers of Physical Sciences Oncology Centers to enrich collaborations and disseminate technological advances throughout the network. By this approach the impact of this research should be felt far more widely than ordinary individual investigator projects.
期刊论文(142)
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会议论文
DOI: 10.1371/journal.pone.0111487
发表时间: 2014
期刊: PloS one
影响因子: 3.7
作者: [Chandrasekaran S, Marshall JR, Messing JA, Hsu JW, King MR]
通讯作者: King MR
DOI: 10.1007/s12195-015-0381-z
发表时间: 2015
期刊: CELLULAR AND MOLECULAR BIOENGINEERING
影响因子: 2.8
作者: [Li, Jiahe, Sharkey, Charles C., Huang, Dantong, King, Michael R.]
通讯作者: King, Michael R.
DOI: 10.1021/ac400105e
发表时间: 2013-03-19
期刊: ANALYTICAL CHEMISTRY
影响因子: 7.4
作者: [Latulippe, David R., Szeto, Kylan, Ozer, Abdullah, Duarte, Fabiana M., Kelly, Christopher V., Pagano, John M., White, Brian S., Shalloway, David, Lis, John T., Craighead, Harold G.]
通讯作者: Craighead, Harold G.
Physicochemical regulation of endothelial sprouting in a 3D microfluidic angiogenesis model.
3D微流血管生成模型中内皮发芽的物理化学调节。
DOI: 10.1002/jbm.a.34587
发表时间: 2013-10
期刊: JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A
影响因子: 4.9
作者: [Verbridge, Scott S., Chakrabarti, Anirikh, DelNero, Peter, Kwee, Brian, Varner, Jeffrey D., Stroock, Abraham D., Fischbach, Claudia]
通讯作者: Fischbach, Claudia
共 100 条
    Biodistribution and PK modeling of rat vs. human systems
    • 批准号:
      10359139
    • 项目类别:
    • 资助金额:
      $78.94万
    • 财政年份:
      2020
    • 负责人:
      MICHAEL L SHULER
    • 依托单位:
    Biodistribution and PK modeling of rat vs. human systems
    • 批准号:
      10079898
    • 项目类别:
    • 资助金额:
      $22.63万
    • 财政年份:
      2020
    • 负责人:
      MICHAEL L SHULER
    • 依托单位:
    Biodistribution and PK modeling of rat vs. human systems
    • 批准号:
      10341323
    • 项目类别:
    • 资助金额:
      $75.42万
    • 财政年份:
      2020
    • 负责人:
      MICHAEL L SHULER
    • 依托单位:
    Diversity Supplement Magnolia Ariza-Nieto
    • 批准号:
      8753396
    • 项目类别:
    • 资助金额:
      $17.11万
    • 财政年份:
      2013
    • 负责人:
      MICHAEL L SHULER
    • 依托单位:
    海外基金