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DESCRIPTION (provided by applicant): Head and neck cancer is one of the top five most common forms of malignancy. One of main problems in head and neck cancer treatment is local regional control and frequent recurrence. In this grant application, we propose to examine a hypothesis that may significantly improve the radiotherapy of H&N cancer. The long-term objective of this project is to characterize the status of the so-called "master switches": hypoxia-inducible factor (HIF) genes, during radiotherapy of head and neck cancer and to exploit such knowledge for potential therapeutic gain. The hypothesis of our project is that HIF-1&2 genes play key roles in determining head and neck (H&N) cancer responses to radiotherapy, and that inhibiting HIF-1&2 activities can enhance the efficacy of H&N cancer radiotherapy. Our project is based on previous studies indicating that hypoxia and both of the HIF-1&2 factors play important roles in determining prognosis of head and neck cancer radiotherapy. In addition, it is based on our new data that indicated HIF factors were activated by radiotherapy independent of hypoxia through the generation of intratumoral nitric oxide, which can stabilize the alpha subunits of the HIF genes. We will conduct experiments to systematically characterize radiation-induced HIF-1 and HIF-2 gene activation in preclinical head and neck cancer models by use of novel molecular imaging and transgenic mouse approaches. Specifically, we will examine the roles of specific nitric oxide synthase genes in radiation-induced HIF-1&2 activation (Specific aim 1). In addition, we will attempt to decipher the molecular mechanism through which nitric oxide mediates radiation-induced HIF-1&2 activation in head and neck cancer radiotherapy (Specific aim 2). Finally, we will evaluate the relative importance of these two factors in head and neck cancer survival after radiotherapy (Specific Aim 3). The proposed studies should provide important insights into the biological mechanisms of radiation-induced activation of the HIF genes and evaluate the efficacy for inhibiting these two factors during head and neck cancer radiotherapy.
期刊论文(12)
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科研奖励(0)
会议论文
Caspase 3 in dying tumor cells mediates post-irradiation angiogenesis.
垂死肿瘤细胞中的 Caspase 3 介导辐射后血管生成。
DOI: 10.18632/oncotarget.5898
发表时间: 2015-10-20
期刊: Oncotarget
影响因子: --
作者: [Feng X, Tian L, Zhang Z, Yu Y, Cheng J, Gong Y, Li CY, Huang Q]
通讯作者: Huang Q
DOI: 10.1371/journal.pcbi.1003461
发表时间: 2014-02
期刊: PLoS computational biology
影响因子: 4.3
作者: [Liu C, Li CY, Yuan F]
通讯作者: Yuan F
DOI: 10.3978/j.issn.2218-676x.2012.05.02
发表时间: 2012-06
期刊: Translational cancer research
影响因子: 0.9
作者: [Kon T, Zhang X, Huang Q, Yang Z, Liu S, Yan B, Li F, Wang H, Li CY]
通讯作者: Li CY
DOI: 10.1016/j.stem.2010.09.003
发表时间: 2010-10-08
期刊: CELL STEM CELL
影响因子: 23.9
作者: [Li, Fang, He, Zhimin, Shen, Jingping, Huang, Qian, Li, Wenrong, Liu, Xinjian, He, Yujun, Wolf, Frank, Li, Chuan-Yuan]
通讯作者: Li, Chuan-Yuan
11
    Targeting ATM to boost systemic effects of radiotherapy and immunotherapy
    • 批准号:
      10368980
    • 项目类别:
    • 资助金额:
      $51.6万
    • 财政年份:
      2021
    • 负责人:
      Chuan-Yuan Li
    • 依托单位:
    Targeting ATM to boost systemic effects of radiotherapy and immunotherapy
    • 批准号:
      10211705
    • 项目类别:
    • 资助金额:
      $52.66万
    • 财政年份:
      2021
    • 负责人:
      Chuan-Yuan Li
    • 依托单位:
    Necroptotic genes in cancer cellular response to radiation
    • 批准号:
      9322798
    • 项目类别:
    • 资助金额:
      $44.3万
    • 财政年份:
      2017
    • 负责人:
      Chuan-Yuan Li
    • 依托单位:
    Targeting apoptotic caspases to enhance cancer radiotherapy
    • 批准号:
      10064085
    • 项目类别:
    • 资助金额:
      $46.78万
    • 财政年份:
      2017
    • 负责人:
      Chuan-Yuan Li
    • 依托单位:
    海外基金