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Genetic study on interaction among carcinogenesis, proliferation and progression in oral epithelia and mesenchymal tissues

Genetic study on interaction among carcinogenesis, proliferation and progression in oral epithelia and mesenchymal tissues
口腔上皮和间质组织致癌、增殖和进展之间相互作用的遗传学研究
批准号:
13470436
负责人:
INOUE Shingo
金额:
$9.28万
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:
2001
资助国家:
日本
项目状态:
已结题
起止时间:
2001 至 2004

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中文摘要
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英文摘要
I.The expression of cancer related genes (p53,mdm2,p14) in oral squamous cell carcinomas and leukoplakia were examined immunohistochemically.1.The expression rate of p53 was 23.2%, that of mdm2 was 44.6%, and that of p14 was 56.0% in leukoplakia. Only p14 expression was correlated with cellular atypism, and as atypism was severe, the rate of expression was reduced. The expression rate of p53 was 40.8%, that of mdm2 was 46.9% and that of p14 was 22.9% in oral squamous cell carcinomas, and as differentiation was poor, the expression rate was reduced.2.The expression rate of mdm2(+)/p14(+) was 85% in normal gingiva, 37% in leukoplakia (carcinogenesis), 30% in leukoplakia(no carcinogenesis), and 19% in squamous cell carcinomas. As atypical cells increased, the simultaneous expression rate of mdm2 and p14 was reduced. In squamous cell carcinoma, as differentiation was poor, the simultaneous expression rate of mdm2 and p14 was reduced.3.The only mdm2 expression rate was 0% in normal gingiva, 12% in leukoplakia (carcinogenesis) and 27.8% in oral squamous cell carcinomas. The expression of mdm2 was correlated with malignancy.4.The expression rate of mdm2 in stroma was 25.8% (non carcinogenesis) and 48.0% (carcinogenesis) in leukoplakia. According to the TNM classification, the mdm2 expression rate of early tumor stage cases was higher than that of advanced tumor stage cases.The expression rate of mdm2 of stroma was 7.7% in normal gingiva and 85% in oral lichen planus.
期刊论文(12)
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会议论文
口腔癌162例中の晩期再発扁平上皮癌7例の臨床病態的検討(1981〜1990)
162例口腔癌中7例晚期复发鳞癌的临床及病理检查(1981-1990年)
DOI: --
发表时间: 2003
期刊: 広大歯誌 35巻第1号
影响因子: --
作者: [Khaleda Akhter, 東森秀年 他]
通讯作者: 東森秀年 他
Clinicopathologic investigations of seven late recurrences of 162 oral squamous cell carcinomas (1981-1990)
162例口腔鳞状细胞癌7例晚期复发的临床病理学研究(1981-1990)
DOI: --
发表时间: 2003
期刊: J.Hiroshima Univ.Dent.Soc. 35(1)
影响因子: --
作者: [Khaleda Akhter, 東森秀年 他, 信森 剛, Khaleda Akhter, Hidetoshi Tohmori]
通讯作者: Hidetoshi Tohmori
Bological characteristics of two new cell straines isolated from a primary squamous cell carcinoma of the tongue and a nodal metastasis
从舌原发性鳞状细胞癌和淋巴结转移中分离出的两种新细胞株的生物学特征
DOI: --
发表时间: 2003
期刊: J.Hiroshima Univ.Dent.Soc. 35(1)
影响因子: --
作者: [Khaleda Akhter, 東森秀年 他, 信森 剛, Khaleda Akhter, Hidetoshi Tohmori, Takeshi Nobumori]
通讯作者: Takeshi Nobumori
Study on expression of 5-fluorouracil (5-FU) related enzymes and acquired resistance to 5-FU in oral squamous cell carcinoma.
口腔鳞癌中5-氟尿嘧啶(5-FU)相关酶的表达及对5-FU获得性耐药的研究
DOI: --
发表时间: 2003
期刊: 広大歯誌 35巻第1号
影响因子: --
作者: [Khaleda Akhter]
通讯作者: Khaleda Akhter
6
    Development of differential diagnostics for various arboviruses
    • 批准号:
      18K08434
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.91万
    • 财政年份:
      2018
    • 负责人:
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    Study of the effect of Epidermal cell differentiation inhibitor on differentiation and proliferation of squamous cell carcinomas
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      08672310
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $1.47万
    • 财政年份:
      1996
    • 负责人:
      INOUE Shingo
    • 依托单位:
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    Circ_0001313/miR-338-3p经P53调控铁死亡降低结直肠癌放化疗敏感性的机制
    基于影像组学与代谢组学特征图谱的机器学习模型在P53突变型子宫内膜癌中的临床应用研究
    • 批准号:
      2026JJ82384
    • 项目类别:
      省市级项目
    • 资助金额:
      --
    • 批准年份:
      2026
    • 负责人:
      颜志鹏
    • 依托单位:
    APR-246靶向突变p53通路逆转DLBCL耐药的分子功能及机制研究
    • 批准号:
      JCZRQNB202600696
    • 项目类别:
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    • 资助金额:
      --
    • 批准年份:
      2026
    • 负责人:
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    黄芩素通过p53信号通路逆转胃黏膜肠上皮化生的机制研究