Measurement of antibodies against tumor suppressor gene products in health screening for lung cancer

肺癌健康筛查中抑癌基因产物抗体的测定

基本信息

  • 批准号:
    14570550
  • 负责人:
  • 金额:
    $ 1.73万
  • 依托单位:
  • 依托单位国家:
    日本
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 财政年份:
    2002
  • 资助国家:
    日本
  • 起止时间:
    2002 至 2003
  • 项目状态:
    已结题

项目摘要

To establish serum markers for early diagnosis of lung cancer, we developed methods to detect autoantibodies against tumor suppressor gene products. In addition, we conducted a large scale survey to confirm the performance of these markers to detect lung cancer among healthy people. First, we developed an immunoblotting assay against bacterially generated GST-RB fusion proteins. Using this assay, we examined 45 sera from lung cancer patients and 30 healthy volunteers. We found 13.3% of lung cancer patients had serum antibodies against GST-Rb fusion proteins, while none of 30 normal volunteers had these antibodies. Secondly, we developed Enzyme-Linked Immunosorbent Assay (ELISA) for detecting anti-Rb antibodies to facilitate measurement a lot of samples. This ELISA system could detect elevated anti-Rb antibodies in serum of lung cancer patients, but not in normal volunteers. These results indicated the usefulness of our measuring systems for anti-Rb antibodies. Thirdly, to study the performance of these measuring systems in health screening for lung cancer, we got the approval of the ethical committee of Tottori University, and of local self-governing bodies in Tottori prefecture. After that, we started to recruit healthy volunteers who provide their serum and information of disease experience in group health examination settings. We are planning to continue this study for more three years. In summary, supported by this grant, we made two sensitive methods to detect autoantibodies against tumor suppressor gene products, verified their usefulness in lung cancer patients as tumor makers, and started mass survey to confirm their performance in health screening for lung cancer. We believe this will lead to the development of a new serum indicator for early detection of lung cancer.
为了建立肺癌早期诊断的血清标志物,我们开发了检测抗肿瘤抑制基因产物的自身抗体的方法。此外,我们进行了一项大规模调查,以确认这些标志物在健康人群中检测肺癌的性能。首先,我们开发了针对细菌产生的GST-RB融合蛋白的免疫印迹分析。用此方法检测了45例肺癌患者和30例健康志愿者的血清。我们发现13.3%的肺癌患者血清中有抗GST-Rb融合蛋白的抗体,而30名正常志愿者中没有这些抗体。其次,我们开发了检测抗Rb抗体的酶联免疫吸附试验(ELISA),以方便大量样本的测量。该ELISA检测系统能检测出肺癌患者血清中抗Rb抗体的升高,但不能检测到正常人血清中抗Rb抗体的升高。这些结果表明,我们的抗Rb抗体的测量系统的有用性。第三,为了研究这些测量系统在肺癌健康筛查中的性能,我们得到了鸟取大学伦理委员会和鸟取县地方自治团体的批准。之后,我们开始招募健康志愿者,他们在团体健康检查设置中提供他们的血清和疾病经历信息。我们计划继续这项研究三年以上。综上所述,在该基金的支持下,我们建立了两种灵敏的检测肿瘤抑制基因产物自身抗体的方法,验证了它们作为肿瘤标记物在肺癌患者中的有用性,并开始进行大规模调查,以确认它们在肺癌健康筛查中的性能。我们相信这将导致一种新的血清指标的发展,用于肺癌的早期检测。

项目成果

期刊论文数量(20)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Sako T, Burioka N, Yasuda K, Shimizu E., et al.: "Cellular immune profile in patients with non-small cell lung cancer after weekly paclitaxel therapy."Acta Oncol. 43. 5-7 (2004)
Sako T、Burioka N、Yasuda K、Shimizu E. 等人:“每周紫杉醇治疗后非小细胞肺癌患者的细胞免疫特征。”Acta Oncol。
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    0
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  • 通讯作者:
Iwata K, Shimizu E, et al.: "Trichostatin A, a histone deacetylase inhibitor, down-regulates lnterleukin-12 transcription in SV-4O-transformed lung epithelial cells"Cell Immunol.. 218(1-2). 26-33 (2002)
Iwata K、Shimizu E 等人:“曲古抑菌素 A,一种组蛋白脱乙酰酶抑制剂,下调 SV-4O 转化的肺上皮细胞中白细胞介素 12 的转录”《细胞免疫学》218(1-2)。
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  • 影响因子:
    0
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Igishi T, Hitsuda Y, Shimizu E., et al.: "Elevated urinary 8-hydroxydeoxyguanosine, a biomarker of oxidative stress, and lack of association with antioxidant vitamins in chronic obstructive pulmonary disease."Respirology. 8. 455-460 (2003)
Igishi T、Hitsuda Y、Shimizu E. 等人:“尿 8-羟基脱氧鸟苷升高,这是氧化应激的生物标志物,并且与慢性阻塞性肺病中的抗氧化维生素缺乏相关性。”呼吸学。
  • DOI:
  • 发表时间:
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  • 影响因子:
    0
  • 作者:
  • 通讯作者:
Sako T, Burioka N, Yasuda K, Tomita K, Miyata M, Kurai J, Chikumi H, Watanabe M, Suyama H, Fukuoka Y, Ueda Y, Shimizu E.: "Cellular immune profile in patients with non-small cell lung cancer after weekly paclitaxel therapy."Acta Oncol.. 43(1). 5-7 (2004)
Sako T、Burioka N、Yasuda K、Tomita K、Miyata M、Kurai J、Chikumi H、Watanabe M、Suyama H、Fukuoka Y、Ueda Y、Shimizu E.:“非小细胞肺癌患者的细胞免疫特征
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
Chikumi H, Barac A, Behbahani B, Gutkind JS, et al.: "Homo- and hetero-oligomerization of PDZ-RhoGEF, LARG and p115RhoGEF by their C-terminal region regulates their in vivo Rho GEF activity and transforming potential."Oncogene. 23. 233-240 (2004)
Chikumi H、Barac A、Behbahani B、Gutkind JS 等人:“PDZ-RhoGEF、LARG 和 p115RhoGEF 通过 C 端区域的同源和异源寡聚可调节其体内 Rho GEF 活性和转化潜力。”Oncogene
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SHIMIZU Eiji其他文献

SHIMIZU Eiji的其他文献

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{{ truncateString('SHIMIZU Eiji', 18)}}的其他基金

New method of cognitive behavior therapy for adolescent depression considering the gender difference in mind and brain, and social development
考虑心脑性别差异和社会发展的青少年抑郁症认知行为治疗新方法
  • 批准号:
    24659538
  • 财政年份:
    2012
  • 资助金额:
    $ 1.73万
  • 项目类别:
    Grant-in-Aid for Challenging Exploratory Research
Development of novel therapy for malignant mesothelioma by controllingADCC activity.
通过控制 ADCC 活性开发恶性间皮瘤的新疗法。
  • 批准号:
    22590863
  • 财政年份:
    2010
  • 资助金额:
    $ 1.73万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Search for the epigenetic transcription factor related to fear extinction
寻找与恐惧消退相关的表观遗传转录因子
  • 批准号:
    21500344
  • 财政年份:
    2009
  • 资助金额:
    $ 1.73万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Sensory gating deficits in schizophrenia and midkine deficiency
精神分裂症和中期因子缺乏症的感觉门控缺陷
  • 批准号:
    18500289
  • 财政年份:
    2006
  • 资助金额:
    $ 1.73万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Measurement of newly developed tumor markers and molecular markers in health screening for lung cancer
新开发的肿瘤标志物和分子标志物在肺癌健康筛查中的测定
  • 批准号:
    18590849
  • 财政年份:
    2006
  • 资助金额:
    $ 1.73万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Gene therapy for lung cancer using tumor suppressor gene product as molecular target
以抑癌基因产物为分子靶点的肺癌基因治疗
  • 批准号:
    09670615
  • 财政年份:
    1997
  • 资助金额:
    $ 1.73万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Basic and clinical research of peripheral blood stem cell transplant (PBSCT) in chemotherapy for lung cancer
外周血干细胞移植(PBSCT)在肺癌化疗中的基础与临床研究
  • 批准号:
    06670615
  • 财政年份:
    1994
  • 资助金额:
    $ 1.73万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (C)

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与作为单倍体不足和隐性肿瘤抑制基因 KMT2C 相关的乳腺癌建模
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正常和恶性造血过程中增强 RNA 介导的肿瘤抑制基因表达
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共存多种抑癌基因突变的 KRAS 突变肺癌细胞治疗靶点的研究
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