Measurement of newly developed tumor markers and molecular markers in health screening for lung cancer
Measurement of newly developed tumor markers and molecular markers in health screening for lung cancer
批准号:
18590849
负责人:
SHIMIZU Eiji
金额:
$2.04万
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:
2006
资助国家:
日本
项目状态:
已结题
起止时间:
2006 至 2007
中文摘要
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英文摘要
To establish serum markers for early diagnosis of lung cancer, we developed methods to detect a candidate for molecular marker. In addition, we conducted a large scale survey to confirm the performance of this marker in combination with known tumor markers, to detect lung cancer among healthy people. First, we developed Enzyme-Linked Immunosorbent Assay (ELISA) for detecting soluble ULBP-2. This ELISA system could detect elevated ULBP-2 in serum of lung cancer patients, but not in normal volunteers. These results indicated the usefulness of the ELISA systems. Secondly, to study the performance of the molecular and tumor markers in health screening for lung cancer, we recruited healthy volunteers in group health examination settings. We measured ProGRP, ULBP-2, anti-p53 autoantibody, and cotinine as a marker for small cell lung cancer, non-small cell lung cancer, lung cancer, and smoking habits, respectively. As a result, we revealed that these markers are independent indicators. Thirdly, we developed a new recruitment system to obtain complete personal information of the participants. We got 163 new participants using this system. Serum ProGRP was elevated in two (?20.0 pg/mL), but not exceed a normal level (46.0 pg/mL). Serum ULBP-2 was mildly (2 - 10 ng/ml), moderately (10 - 100 ng/ml), or highly (?100 ng/ml) elevated in five, three, or one subjects, respectively. We are planning to follow up this study population to find the onsets of lung cancer. In summary, supported by this grant, we made a sensitive method to detect a potential candidate of the molecular marker of lung cancer, verified the usefulness of it in combination with kwon tumor maker and autoantibody in cancer screening. In addition, we developed a new system of mass survey to confirm their performance in health screening settings. We believe this will lead to the development of new serum indicators for early detection of lung cancer.
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肺癌細胞株におけるセツキシマブを介した抗体依存的細胞傷害活性の検討(Antibody-Dependent Cellular Cytotoxicity Mediated by Cetuximab against Lung Cancer Cell Lines)
西妥昔单抗介导的针对肺癌细胞系的抗体依赖性细胞毒性
DOI:
--
发表时间:
2007
期刊:
影响因子:
--
作者:
[倉井 淳, 他]
通讯作者:
他
Antibody-dependent cellular cytotoxicity mediated by cetuximab against lung cancer lines.
西妥昔单抗介导的针对肺癌细胞系的抗体依赖性细胞毒性。
DOI:
--
发表时间:
2007
期刊:
Clin Cancer Res 13(5)
影响因子:
--
作者:
[Kurai J, et al.]
通讯作者:
et al.
DOI:
10.1158/1078-0432.ccr-06-1726
发表时间:
2007-03-01
期刊:
CLINICAL CANCER RESEARCH
影响因子:
11.5
作者:
[Kurai, Jun, Chikumi, Hiroki, Shimizu, Eiji]
通讯作者:
Shimizu, Eiji
DOI:
10.3892/ijo.30.1.187
发表时间:
2007
期刊:
International journal of oncology
影响因子:
5.2
作者:
[M. Morita;H. Suyama;T. Igishi;Y. Shigeoka;M. Kodani;Kiyoshi Hashimoto;K. Takeda;T. Sumikawa;E. Shimizu]
通讯作者:
M. Morita;H. Suyama;T. Igishi;Y. Shigeoka;M. Kodani;Kiyoshi Hashimoto;K. Takeda;T. Sumikawa;E. Shimizu
DOI:
10.3892/ijo.32.3.683
发表时间:
2008-03
期刊:
International journal of oncology
影响因子:
5.2
作者:
[T. Sumikawa;Y. Shigeoka;T. Igishi;H. Suyama;A. Yamasaki;Kiyoshi Hashimoto;S. Matsumoto;K. Takeda;Y. Ueda;E. Shimizu]
通讯作者:
T. Sumikawa;Y. Shigeoka;T. Igishi;H. Suyama;A. Yamasaki;Kiyoshi Hashimoto;S. Matsumoto;K. Takeda;Y. Ueda;E. Shimizu
共 11 条
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组蛋白乙酰化对MSCs微环境适应性的调控作用及机制
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项目类别:青年科学基金项目
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