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Regulator of G-protein Signalling-5: a key modulator of vascular maturation and the

Regulator of G-protein Signalling-5: a key modulator of vascular maturation and the
G 蛋白信号传导调节因子 5:血管成熟和血管成熟的关键调节因子
批准号:
nhmrc : 458627
负责人:
Karin Eidne
金额:
$36.57万
依托单位国家:
澳大利亚
项目类别:
NHMRC Project Grants
财政年份:
2007
资助国家:
澳大利亚
项目状态:
已结题
起止时间:
2007-01-01 至 2009-12-31

项目摘要

项目成果

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中文摘要
翻译
肿瘤逐渐生长,部分原因是它们逃脱了免疫系统的破坏。新的血管通过一种叫做血管生成的过程在肿瘤内生长,这反过来又阻止了抗病细胞的运行。然而,我们现在发现,通过使血管正常化来逆转血管生成是可能的。这实际上意味着屏障被打破,肿瘤可以向免疫系统或抗癌药物开放。此外,我们已经确定了一种蛋白质,它似乎对正常化非常重要,这一过程目前尚不清楚。这项建议延续了我们在血管正常化方面的开创性工作,并将使用具有最高临床相关性的模型来研究肿瘤中血管重构的动力学。我们的方法与目前的血管生成研究不同,目前的研究只是试图阻断或破坏滋生肿瘤的血管。我们希望我们的发现能带来高度特异和有效的抗肿瘤疗法。此外,肿瘤中的血管生长与体内的其他血管过程有着惊人的相似之处,这对高血压和动脉粥样硬化等重大和常见的人类疾病具有重要意义。在我们新建立的疾病模型中,我们现在有了研究这些过程及其异常的工具。通过对这些疾病的深入了解,我们将能够开发出阻止疾病进展的新方法。
英文摘要
Tumours progressively grow in part because they escape destruction by the immune system. New blood vessels grow inside tumours by a process called angiogenesis, which in turn stops disease-fighting cells in their tracks. However, we have now discovered that it is possible to reverse angiogenesis by normalising the blood vessels. This effectively means the barriers are broken down and the tumour can be opened to the immune system or cancer fighting drugs. Furthermore, we have identified a protein which appears to be very important for normalisation, a process which is currently not well understood. This proposal continues our pioneering work on vessel normalisation and will use models of highest clinical relevance to study the dynamics of vessel remodelling in tumours. Our approach is different to current angiogenesis research which simply tries to block or destroy the blood vessels that feed tumours. We expect our findings to lead to highly specific and effective anti-tumour therapies. Moreover, vessel growth in tumours has striking parallels to other vascular processes in the body, which have important implications for major and common human diseases such as high blood pressure and atherosclerosis. We now have the tools to study these processes and their abnormalities in our newly established disease model. By gaining insight into these disorders we will be able to develop novel approaches to stop disease progression.
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Novel interactions between GnRH receptor and E2F4 transcription factor.
  • 批准号:
    nhmrc : 303256
  • 项目类别:
    NHMRC Project Grants
  • 资助金额:
    $30.86万
  • 财政年份:
    2004
  • 负责人:
    Karin Eidne
  • 依托单位:
Molecular mechanisms underlying G protein coupled receptor signaling
  • 批准号:
    nhmrc : 299811
  • 项目类别:
    NHMRC Project Grants
  • 资助金额:
    $39.81万
  • 财政年份:
    2004
  • 负责人:
    Karin Eidne
  • 依托单位:
Equipment Grant 2002
  • 批准号:
    nhmrc : 264402
  • 项目类别:
    NHMRC Infrastructure Grants
  • 资助金额:
    $0.69万
  • 财政年份:
    2003
  • 负责人:
    Karin Eidne
  • 依托单位:
Development of BRET detection systems: tools for functional proteomics and drug discovery
  • 批准号:
    nhmrc : 254646
  • 项目类别:
    NHMRC Development Grants
  • 资助金额:
    $25.09万
  • 财政年份:
    2003
  • 负责人:
    Karin Eidne
  • 依托单位:
国内基金
海外基金
子宫内膜间质与巨噬细胞之间通过Protein S-MerTK-Apelin信号对 话促进子宫腺肌病蜕膜化缺陷的机制研究
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  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2024
  • 负责人:
    吕海宁
  • 依托单位:
有翅与无翅蚜虫差异分泌唾液蛋白Cuticular protein在调控植物细胞壁免疫中的功能
  • 批准号:
    32372636
  • 项目类别:
    面上项目
  • 资助金额:
    50.00万元
  • 批准年份:
    2023
  • 负责人:
    郭慧娟
  • 依托单位:
原发性开角型青光眼中SIPA1L1促进小梁网细胞外基质蛋白累积升高眼压的作用机制
  • 批准号:
    82371054
  • 项目类别:
    面上项目
  • 资助金额:
    49.00万元
  • 批准年份:
    2023
  • 负责人:
    郭涛
  • 依托单位:
胆固醇合成蛋白CYP51介导线粒体通透性转换诱发Th17/Treg细胞稳态失衡在舍格伦综合征中的作用机制研究
  • 批准号:
    82370976
  • 项目类别:
    面上项目
  • 资助金额:
    48.00万元
  • 批准年份:
    2023
  • 负责人:
    郑凌艳
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