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Apoptosis in the process of carcinogenesis of oral precancerous lesions

Apoptosis in the process of carcinogenesis of oral precancerous lesions
口腔癌前病变癌变过程中的细胞凋亡
批准号:
06454572
负责人:
NAGUMO Masao
金额:
$4.1万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (B)
财政年份:
1994
资助国家:
日本
项目状态:
已结题
起止时间:
1994 至 1995

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中文摘要
翻译
我们用免疫组化方法对口腔白斑、口腔白斑继发癌和口腔鳞状细胞癌标本中lewis^y (le^y)抗原、tgf - α、P53蛋白、bcl-2蛋白和PCNA的表达进行了研究。采用Tunel法检测DNA片段,研究细胞凋亡的发生情况。此外,我们在体外研究了抗肿瘤药物和硝普钠(SNP)是否能诱导口腔上皮细胞凋亡。我们还检测了细胞凋亡过程中基因表达的变化。实验结果如下:1。Le^y抗原和bcl-2蛋白在口腔癌组织中的表达较白斑组织弱。相反,tgf - α、P53蛋白和PCNA在口腔癌中的表达强于在白斑中的表达。在白斑中,Le^y抗原和bcl-2蛋白的表达随上皮异常增生的分级而降低,而tgf - α、P53蛋白和PCNA的表达随上皮异常增生的分级而升高。Le^y抗原和bcl-2蛋白的表达随恶性转化而降低。Tunel法检测的DNA片段在口腔白斑中较口腔癌多发。5-Fu、顺铂和SNP均可诱导口腔上皮细胞(NA)凋亡,凋亡过程中c-myc、c-myb、p53 mRNA表达下调。
英文摘要
We investigated the expression of lewis^y (le^y) antigen, TGF-alpha, P53 protein, bcl-2 protein and PCNA immunohistochemically in the specimens which were obtained from patients with leukoplakia, cancer developed from leukoplakia and oral squamous cell carcinoma. Further, occurrence of apoptosis in those specimens was studied by detecting the fragmentation of DNA using Tunel method. In addition, we examined in vitro whether apoptosis could be induced in oral epithelial cells by anticancer drugs and sodium nitroprusside (SNP). We also examined the changes in the expression of genes during apoptosis.The results obtained were as follows :1.Le^y antigen and bcl-2 protein in oral cancer were expressed more weakly than those in leukoplakia. On the contrary, TGF-alpha, P53 protein and PCNA in oral cancer were expressed more strongly than those in leukoplakia.2.The expression of Le^y antigen and bcl-2 protein decreased with the grade of epithelial dysplasia in leukoplakia, whereas the expression of TGF-alpha, P53 protein and PCNA increased with the grade of epithelial dysplasia.3.The expression of Le^y antigen and bcl-2 protein decreased with malignant transformation.4.DNA fragmentation detected by Tunel method occurred more frequently in leukoplakia than in oral cancer.5-Fu, cisplatin and SNP could induced apoptosis in oral epithelial cells (NA) and mRNA expression of c-myc, c-myb, p53 was downregulated during apoptosis.
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中村雅子 他: "白板症の免疫組織化学的検討-上皮異形成とLe^y抗原およびP53蛋白発現との関連-" 日本口腔外科学会雑誌. 42(印刷中). (1996)
Masako Nakamura 等人:“白斑的免疫组织化学研究 - 上皮发育不良与 Le^y 抗原和 P53 蛋白表达之间的关系”,日本口腔颌面外科学会杂志 42(出版中)。
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中村雅子,他: "白板症より癌化した7症例の臨床病理学的検討" 日本口腔外科学会雑誌. 41. 767-773 (1995)
Masako Nakamura 等人:“白斑癌 7 例的临床病理学研究”日本口腔颌面外科杂志 41. 767-773 (1995)。
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共 20 条
    Prediction of malignant transformation of oral precancerous lesions by analyzing gene expression profiles and gene polymorphism.
    • 批准号:
      15209070
    • 项目类别:
      Grant-in-Aid for Scientific Research (A)
    • 资助金额:
      $25.71万
    • 财政年份:
      2003
    • 负责人:
      NAGUMO Masao
    • 依托单位:
    The participation of p53 independent pathway in the process of oral carcinogenesis
    • 批准号:
      13470439
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $10.43万
    • 财政年份:
      2001
    • 负责人:
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    • 依托单位:
    The effects of CDK inhibitors and PI3 kinase related kinase on the carcinogenesis from precancerous lesions
    • 批准号:
      11470443
    • 项目类别:
      Grant-in-Aid for Scientific Research (B).
    • 资助金额:
      $8.45万
    • 财政年份:
      1999
    • 负责人:
      NAGUMO Masao
    • 依托单位:
    Development of detection method of metastasis from squamous cell carcinoma of head and neck using peripheral blood
    • 批准号:
      11557163
    • 项目类别:
      Grant-in-Aid for Scientific Research (B).
    • 资助金额:
      $7.68万
    • 财政年份:
      1999
    • 负责人:
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