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Multivariate analysis of chemotherapeutic effect for oral cancer by tumor markers

Multivariate analysis of chemotherapeutic effect for oral cancer by tumor markers
肿瘤标志物对口腔癌化疗效果的多因素分析
批准号:
09470459
负责人:
YAMAGUCHI Akira
金额:
$4.03万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
1997
资助国家:
日本
项目状态:
已结题
起止时间:
1997 至 1999

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英文摘要
Part I. Plasma levels of GST-π activity were quantitatively analyzed in 82 patients with oral squamous cell carcinoma (S.C.C.), and the results were correlated with clinicopathological variables including patient outcome. The levels were correlated with nodal metastasis and clinical stage. Moreover, the patients with higher level of GST-π were significantly poorer in clinical outcome, indicating the usefulness of GST-π in estimating the prognosis of patients with oral S.C.C.Part II. P53 protein expression in 174 primary oral S.C.C. Was examined by immunohistochemistry. Diffuse p53 protein expression was correlated with clinicopathological variables including patient outcome. Furthermore, the prognosis in patients with oral S.C.C. Of diffuse p53 protein expression were poorer than those of patients with oral S.C.C. Of focal p53 protein expression and negative p53 expression. Our data confirm that p53 was useful as a prognostic indicator in oral S.C.C.Part III. P53 status was tested in 35 oral S.C.C. From the tumors examined in the part II study, using methods of immunohistochemistry for p53 protein expression and PCR-SSCP for screening of p53 gene mutation. There were 2 tumors with mutation (25%) in 8 tumors of focal p53 protein expression, while 16 tumors with mutation (80%) in 20 tumors of diffuse p53 protein expression. These data indicated that most of tumors with diffuse p53 protein expression were p53 gene mutation.Part IV. Expression of p53 protein and β-catenine in 192 oral S.C.C. Was examined by immunohistochemistry, and the results were correlated with clinicopathological variables including patient outcome. P53 positive and β-catenine abnormal expression were associated with clinical progression of the disease, tumor invasion and poor prognosis, suggesting that the combination assay of p53 and β-catenine was useful in evaluating the malignant protein of oral S.C.C.
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Tanaka, N., et al: "Imunohistochemical expression of p130 oncogene in oral squamous cell carcinoma referred to histopathological findings"Oral Oncology IV. 75-78 (1999)
Tanaka, N. 等人:“口腔鳞状细胞癌中 p130 癌基因的免疫组织化学表达参考组织病理学结果”口腔肿瘤学 IV。
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通讯作者:
Miyazaki Akihiro et al: "Cytotoxicity of Histocompatibility Leukocyto Antigen-DR8-restricted CD4^+killer T Cell against Human Autologous Squamoas Cell Carcinoua" Jpn.T.Cancer Res. Fel88. 191-197 (1997)
Miyazaki Akihiro 等人:“组织相容性白细胞抗原-DR8 限制性 CD4^ 杀伤性 T 细胞对人自体鳞状细胞癌的细胞毒性”Jpn.T.Cancer Res。
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Fundamental research of practical use of Super Fine Silica Powder Slurry Materials for countermeasure against liquefaction
  • 批准号:
    26420485
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 资助金额:
    $2.83万
  • 财政年份:
    2014
  • 负责人:
    YAMAGUCHI Akira
  • 依托单位:
Involvement in alpha-synuclein function and pathology in lysosomal storage diseases
  • 批准号:
    25460500
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
  • 资助金额:
    $3.24万
  • 财政年份:
    2013
  • 负责人:
    YAMAGUCHI Akira
  • 依托单位:
Development of micro-SQUID-NMR for low temperature condensed matter physics
  • 批准号:
    24654109
  • 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:
    YAMAGUCHI Akira
  • 依托单位:
Elucidation of the mechanisms underlying in the immunological abnormalities of lysosomal storage diseases
  • 批准号:
    23790448
  • 项目类别:
    Grant-in-Aid for Young Scientists (B)
  • 资助金额:
    $2.83万
  • 财政年份:
    2011
  • 负责人:
    YAMAGUCHI Akira
  • 依托单位: