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Molecular Genetics of the Heterogeneiety of the Tumor Perturbing Cacer Treatment

Molecular Genetics of the Heterogeneiety of the Tumor Perturbing Cacer Treatment
肿瘤干扰癌症治疗异质性的分子遗传学
批准号:
16390381
负责人:
INOUE Hiroshi
金额:
$9.15万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
2004
资助国家:
日本
项目状态:
已结题
起止时间:
2004 至 2005

项目摘要

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中文摘要
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英文摘要
PurposeTo investigate the genetic base of the heterogeneity of the digestive cancer, two approaches such as 1)DNA microarray analysis combined with laser microdissection for the gene expression of the digestive tract carcinoma and 2)cancer stem cell survey have been conducted.Material and methodCell line and clinically resected tumor specimens were used for the analysis. Human 44k-DNA microarray were purchased from "Agilent technology" and microarray analysis were performed according to the company's instruction. In addition, genomic microarray were performed for 10 cases of esophageal cancer and 5 cased of hepatocellular carcinoma.Results1)Early staged cancer shows no definitive different expression profile from various parts of the tumor, however, in advance staged cancer, a definitive difference of the profile was observed among the portions of the tumor, in particular, superficial luminal parts and deeper invasive portions.2)Expression profiles differ in cases with different histological types.3)Genomic alteration and simultaneous mRNA expression changes were observed in accordance with the histological development of the tumor. In hepatocellular carcinoma, peripheral portion of the tumor shows very faint alteration in both mRNA and genomics. However, in the central portion that reciprocally later developed, histologically showed more aggressive pattern and also manifested very variable alterations in both mRNA and genomics.DiscussionDNA microarray analysis combined with laser microdissection for the gene expression as well as genomic alteration had very powerful potential for the analysis of histologically complexed tumor. More detailed study will clarify the perplexed nature of the human carcinogenesis.
期刊论文(18)
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DOI: 10.3892/ijo.26.1.41
发表时间: 2005
期刊: International journal of oncology
影响因子: 5.2
作者: [Mitsuhiko Ohta;F. Tanaka;H. Yamaguchi;N. Sadanaga;H. Inoue;M. Mori]
通讯作者: Mitsuhiko Ohta;F. Tanaka;H. Yamaguchi;N. Sadanaga;H. Inoue;M. Mori
DOI: 10.1158/0008-5472.can-05-2509
发表时间: 2006-03-01
期刊: CANCER RESEARCH
影响因子: 11.2
作者: [Mimori, K, Ishii, H, Mori, M]
通讯作者: Mori, M
Genetic susceptibility of catechol-O-methyltransferase polymorphism in Japanese patients with breast cancer
日本乳腺癌患者儿茶酚-O-甲基转移酶多态性的遗传易感性
DOI: --
发表时间: 2005
期刊: Oncol Rep 14
影响因子: --
作者: [Inoue, H., et al.]
通讯作者: et al.
DOI: 10.1158/1078-0432.ccr-03-0262
发表时间: 2004-09-01
期刊: CLINICAL CANCER RESEARCH
影响因子: 11.5
作者: [Yoshinaga, K, Inoue, H, Mori, M]
通讯作者: Mori, M
12
    Investigation of soy protein isolate in whole body glucose metabolism
    • 批准号:
      24650487
    • 项目类别:
      Grant-in-Aid for Challenging Exploratory Research
    • 资助金额:
      $2.5万
    • 财政年份:
      2012
    • 负责人:
      INOUE Hiroshi
    • 依托单位:
    The role of IL-17 on NK cell activation.- Analysis for elucidation of inflammation mechanisms.-
    • 批准号:
      24592853
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $3.0万
    • 财政年份:
      2012
    • 负责人:
      INOUE Hiroshi
    • 依托单位:
    Role of histidine in glucose metabolism
    • 批准号:
      23300274
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $11.56万
    • 财政年份:
      2011
    • 负责人:
      INOUE Hiroshi
    • 依托单位:
    Study on circadian changes in sympathetic tone in subtotal nephrectomized rats with heart failure
    • 批准号:
      23591033
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $3.33万
    • 财政年份:
      2011
    • 负责人:
      INOUE Hiroshi
    • 依托单位:
    海外基金