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EVALUATION OF GRANDE OF MALLIGNANCY ON THE BASIS OF CELL CYCLE ADHESION MOLECULESIN ORAL SQUAMOUS CELL CARCUNOMA

EVALUATION OF GRANDE OF MALLIGNANCY ON THE BASIS OF CELL CYCLE ADHESION MOLECULESIN ORAL SQUAMOUS CELL CARCUNOMA
基于细胞周期粘附分子的口腔鳞状细胞癌恶性程度评价
批准号:
18592222
负责人:
YAMAGUCHI Akira
金额:
$2.26万
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

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中文摘要
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英文摘要
Dysregulation of tumor suppressor gene p53 has been shown to play a significant role in development of a wide variety of human malignancies. Some investigators have suggested that accumulated expression of p53 gene protein is useful as a prognostic indicator in oral squamous cell carcinoma (OSCC), although others have reported conflicting result. The aim of this study is to determine the correlation between the expression of p53 gene protein and the clinicopathological features of 140 OSCC. Tumor biopsies obtained from patients with OSCC were examined for the immunohistochemical detection of p53 gene product with special reference to expression pattern correlated with clinicopathological findings and overall survival. Nuclear accumulation of p53 was visualized as marginal pattern, dispersed pattern, or mixed pattern. Simple evaluation of p53 expression (negative and positive) defined with value of 10% did not provide useful information as to the assessment of oral.cancer However, dispe … More rsed type p53 protein expression significantly correlated with nodal metastasis, differentiation of tumor cell, overall survival and mutation. These finding suggest that p53 expression may, but not p53 positivity, be one of biological makers for the degree of malignancy in OSCC.Genetic and epigenetic alterations in tumor-suppressor genes play important roles in human neoplasia. Ras signaling is often activated in OSCC, although RAS mutations are rarely detected in OSCC patients. In present study, we examined the expression and and methylation statuses of RAS association family (RASSF) genes in OSCC. We frequently detected methlaion of RASSF1 (7/17:41.2%) RASSF2 (12/17:70.6%), RASSF5 (4/17:23.5%) in a panel of OSCC cell lines, as well as in specimens collected from 46 OSCC patient (RASSF1, 6/46, 13.0%; RAsSF2,12/46, 26.1%; RASSF5,5/46,10.9%). Our findings indicate that epigenetic inactivation of RASSF plays a key role in OSCC tumorigenesis, and that RASSF may be an important molecular target for the diagnosis and treatment of OSCC. Less
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舌癌の郭清範囲に関する検討
舌癌切除范围的思考
DOI: --
发表时间: 2006
期刊: 頭頸部癌 34(4)
影响因子: --
作者: [Ueda, G., Sunakawa, H., Nakamori, K., Shinya, T., Tsuhako, W., Tamura, Y., Kosugi, T., Sato, N., Ogi, K., Hiratsuka, H, Ueda G, 仲盛健治, 仲盛健治]
通讯作者: 仲盛健治
IFN-γ induces Q2 NK-mediated antitumor effects against oral aquamous cell carcinoma cells
IFN-γ诱导 Q2 NK 介导的针对口腔水癌细胞的抗肿瘤作用
DOI: --
发表时间: 2007
期刊:
影响因子: --
作者: [仲盛健司, 宮崎晃亘他, 小林 淳一, 山本 崇, Yamaguchi A, Tomihara K]
通讯作者: Tomihara K
口腔癌に対するIFAとIFN-αを併用したsurvivinペプチドワクチンの第一相臨床試験
联合IFA和IFN-α对抗口腔癌的survivin肽疫苗一期临床试验
DOI: --
发表时间: 2007
期刊:
影响因子: --
作者: [Yamaguchi, A, 宮崎 晃亘, 宮崎 晃亘]
通讯作者: 宮崎 晃亘
DOI: --
发表时间: 2007
期刊:
影响因子: --
作者: [Miyazaki, A, Imai T, Yamamoto T, Miyazaki A, 今井 崇, 仲盛 健治, 今井 崇]
通讯作者: 今井 崇
33
    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:
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    • 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:
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    • 依托单位:
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