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The Biological Functions of the SART-1 Family in Differentiation and Carcinogenicity of Adenocarcinomas

The Biological Functions of the SART-1 Family in Differentiation and Carcinogenicity of Adenocarcinomas
SART-1家族在腺癌分化和致癌性中的生物学功能
批准号:
10670521
负责人:
SHICHIJO Shigeki
金额:
$2.18万
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:
1998
资助国家:
日本
项目状态:
已结题
起止时间:
1998 至 1999

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中文摘要
翻译
Molecules involved in regulation of cellular proliferation at the G2/M phase have not yet been fully identified.This study investigated the involvement of a recently identified SART-1 I D 2800 I D 2.Protein demonstrated an ability to bind to DNA,And accumulated in the nucleus when the cells were arrested at G2/M phase.(L)The localization of SART-1 protein was suggested to be in nucleus of eukaryote cells including monkey kidney EBV-transformed Cos7cell and human esophageal cancer TE9cell when the fusion gene with GFP was transfected and observed by conforcal laser microscopy.(2)SART-1 i D2800i D2 protein is sugested to be DNA binding and observed by conforcal microscopy.(2)SART-1-D2800i D2protein is sugested to be DNA-binding of the fected in the fected of the fected.-1 gene induced the G2/M-arrest and suppressed the cell growth of all the cell tested.Furthermore,DNA ladder formation was observed in the SART-1 transfected COS-7and human cancer cells.The transfection of SART-1up-regulated the nuclear expression of cyclin B and cdc2,well known components of maturation-promoting factor.(4)Several candidate genes which encode proteins that had interacted with SART-1protein were isolated by two-hybrid system.(5)Three different SART-1probe protein(N-terminal,middle and C-terminal regions)for far-western blot analysis of SART-1bing probe protein(N-terminal,middle and C-terminal regions)The sequence of the gene will submit to GenBank.(7)SART-1gene was suggested to be expressed in early development of mouse embryo(L4days)by northern blot analysis.(8)Several family genes of SART-1were suggested by northern blot analysis。One of the gene with 3.3 kb consist of approximately l488bp of 5‘-region was identical to SART-1 and encoded a protein with483amino acid.
英文摘要
Molecules involved in regulation of cellular proliferation at the G2/M phase have not yet been fully identified. This study investigated the involvement of a recently identified SART-1ィイD2800ィエD2. Protein demonstrated an ability to bind to DNA, and accumulated in the nucleus when the cells were arrested at G2/M phase.(l) The localization of SART-1 protein was suggested to be in nucleus of eukaryote cells including monkey kidney EBV-transformed Cos 7 cell and human esophageal cancer TE9 cell when the fusion gene with GFP was transfected and observed by conforcal laser microscopy.(2) SART-1ィイD2800ィエD2 protein is suggested to be a DNA-binding protein by the affinity chromatography of cell lysates of the 293T cells transfected with the HAN/SART-1ィイD2800ィエD2 gene.(3) Transfection of SART-1 gene induced the G2/M-arrest and suppressed the cell growth of all the cell tested. Furthermore, DNA ladder formation was observed in the SART-1 transfected COS-7 and human cancer cells. The transfection of SART-1 up-regulated the nuclear expression of cyclin B and cdc2, well known components of maturation-promoting factor.(4) Several candidate genes which encode proteins that had interacted with SART-1 protein were isolated by two-hybrid system.(5) Three different SART-1 probe protein (N-terminal, middle and C-terminal regions) for far-western blot analysis of SART-1 binding protein candidate obtained by two hybrid system were prepared.(6) We found that murine SART-1 genomic DNA suggested to be consist of 20 exsons. The sequence of the gene will submit to GenBank.(7) SART-1 gene was suggested to be expressed in early development of mouse embryo (l4 days) by northern blot analysis.(8) Several family genes of SART-1 were suggested by northern blot analysis. One of the gene with 3.3kb consist of approximately l488 bp of 5'-region was identical to SART-1 and encoded a protein with 483 amino acid.
期刊论文(32)
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Nakao M, Shichijo S, Imaizumi T, Inoue Y, Matsunaga K, Yamada A, Kikuchi M, Tsuda N, Ohta K, Takamori S, Yamana H, Fujita H and Itoh K: "Identification of a gene coding for a new squamous cell carcinoma antigen recognized by the CTL."J. Immunol.. 164. 256
Nakao M、Shichijo S、Imaizumi T、Inoue Y、Matsunaga K、Yamada A、Kikuchi M、Tsuda N、Ohta K、Takamori S、Yamana H、Fujita H 和 Itoh K:“鉴定编码新鳞状细胞的基因
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通讯作者:
Shigeki Shichijo: "A gene encoding antigenic peptides of human squamous cell carcinoma recognized by cytotoxic T lymphocytes."Journal of Experimental Medicine. 187. 277-278 (1998)
Shigeki Shichijo:“编码人类鳞状细胞癌抗原肽的基因,可被细胞毒性 T 淋巴细胞识别。”实验医学杂志。
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Kyogo Itoh: "Cell Therapy"Springer-Verlag Tokyo (in press). (1999)
伊藤京吾:“细胞疗法”Springer-Verlag Tokyo(印刷中)。
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Shichijo S, Nakao M, Imai Y,Takasu H, Kawamoto M, Niiya F, Yang D, Toh Y, Yamana H and ltoh K: "A gene encoding antigenic peptides of human squamous cell carcinoma recognized by cytotoxic T lymphocytes."J. Exp. Med.. 187. 277-288 (1998)
Shichijo S、Nakao M、Imai Y、Takasu H、Kawamoto M、Niiya F、Yang D、Toh Y、Yamana H 和 ltoh K:“编码细胞毒性 T 淋巴细胞识别的人类鳞状细胞癌抗原肽的基因。”J.
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共 30 条
    Detection of IgG antibody reactive to a p53-derived peptide with HLA-A4601 binding motif in breast cancer patients
    • 批准号:
      16591281
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.18万
    • 财政年份:
      2004
    • 负责人:
      SHICHIJO Shigeki
    • 依托单位:
    Identification of a cluster of tumor antigens recognized by CTh of colon cancer patients
    • 批准号:
      14570526
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.18万
    • 财政年份:
      2002
    • 负责人:
      SHICHIJO Shigeki
    • 依托单位:
    Basic study of tumor-vaccine for metastatic epithelial cancer.
    • 批准号:
      12670533
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.05万
    • 财政年份:
      2000
    • 负责人:
      SHICHIJO Shigeki
    • 依托单位:
    Expression of MAGE tumor rejection antigen on lung cancer and application for cancer vaccine
    • 批准号:
      07671491
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $1.47万
    • 财政年份:
      1995
    • 负责人:
      SHICHIJO Shigeki
    • 依托单位:
    海外基金