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Isolation and Identification of Tumor suppressor gene in choriocarcinoma.

Isolation and Identification of Tumor suppressor gene in choriocarcinoma.
绒毛膜癌抑癌基因的分离与鉴定。
批准号:
11671631
负责人:
MATSUDA Takao
金额:
$2.3万
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:
1999
资助国家:
日本
项目状态:
已结题
起止时间:
1999 至 2000

项目摘要

项目成果

MATSUDA Takao的其他基金

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相关文献

中文摘要
翻译
1)我们之前报道了人类7号染色体的纯合缺失存在于绒毛膜癌组织和细胞系中。我们认为7号染色体上的病变处存在抑癌作用。通过STS标记,我们从位于7q11.22的病灶中获得了多个BAC克隆。然后我们将这些 BAC 克隆引入绒毛膜癌细胞系中。用RS544-12D (B6)和RS741-8D (B7)转染的克隆体内致瘤性受到抑制。然后通过使用这些克隆作为探针,我们获得了几个抑制绒毛膜癌细胞系致瘤性的cDNA文库克隆。我们发现这些是假定的绒毛膜癌抑制基因之一。现在我们分析该基因的抑癌活性机制。2)我们制作了减去大量绒毛膜癌cDNA片段的绒毛特异性cDNA文库。其中一种未知基因,名为克隆S31,仅在绒毛中表达,但在绒毛膜癌中不表达。克隆S31大小为1.1kb,编码73个氨基酸,当该克隆导入绒毛膜癌细胞系时具有肿瘤抑制潜力。该S31与牙龈表达的cDNA克隆同源,并且位于幼年牙龈的推定病变附近。
英文摘要
1) We previously reported that the homozygous deletion in human chromosome7 were presented in choriocarcinoma tissues and cell lines. We thought the presence of tumor suppressor effect at that lesion in chromosome7. We have got the several BAC clones from the lesion located at 7q11.22 by using STS marker. Then we introduce these BAC clones into choriocarcinoma cell lines. The clones transfected with RS544-12D (B6) and RS741-8D (B7)were suppressed in vivo tumorigenicity. Then by using these clones for probe we got several cDNA library clones that suppressed the tumorigenicity of choriocarcinoma cell lines. We through that these were one of the putative choriocarcinoma suppressor genes. Now we analyze the mechanisms of tumor suppress activity of the genes.2) We made the villi-specific cDNA library that subtracted by large amount of choriocarcinoma cDNA fragment. One of the unknown gene, named clone S31 expressed only in villi, but not in choriocarcinoma. The size of clone S31 is 1.1 kb, coded 73 amino acids and have tumor suppressive potential when this clone were introduced into choriocarcinoma cell line. This S31 are homologous to gingiva expressed cDNA clone and located near the putative lesion of juvenile gingivatitts.
期刊论文(16)
专著(0)
科研奖励(0)
会议论文
Matsuda et al: "Molecular Biology of Choriocarcinoma. V.Basic knowledge of the malignant tumor in corpus uteri"Obstet.Gynecol (Tokyo). 66. 320-325 (1999)
松田等人:“绒毛膜癌的分子生物学。V.子宫体恶性肿瘤的基础知识”Obstet.Gynecol(东京)。
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松田貴雄 他: "新女性医学体系 第37巻 絨毛性疾患 D.新知見(印刷中)"中山書店. (2000)
Takao Matsuda 等:“新女性医疗系统第 37 卷:绒毛膜疾病 D. 新发现(印刷中)”Nakayama Shoten(2000 年)。
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松田貴雄 他: "8.絨毛癌の分子生物学 V.子宮体部悪性腫瘍の基礎知識"産科と婦人科. 66. 320-325 (1999)
Takao Matsuda等:“8.绒毛膜癌的分子生物学V.子宫体恶性肿瘤的基础知识”妇产科66.320-325(1999)。
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Zhou Y et al: "Involvement of mutations in the DPC4 promoter in endometrial carcinoma development."Molecular Carcinogenesis. 25. 64-72 (1999)
Zhou Y等人:“DPC4启动子突变参与子宫内膜癌的发展。”分子癌发生。
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11
    The functional analysis of the putative choriocarcinoma suppressor gene, HTF12 in choriocarcinoma.
    • 批准号:
      15591759
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $1.54万
    • 财政年份:
      2003
    • 负责人:
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    • 依托单位:
    Relationship between a variety of criteria and human fallacies
    • 批准号:
      14310045
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $4.29万
    • 财政年份:
      2002
    • 负责人:
      MATSUDA Takao
    • 依托单位:
    The analysis of OS-4 like gene and homeo protein like gene as a putative choriocarcinoma suppressor gene.
    • 批准号:
      13671728
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.43万
    • 财政年份:
      2001
    • 负责人:
      MATSUDA Takao
    • 依托单位:
    Perception of three-dimensional structure based on two-dimensional motion information
    • 批准号:
      10610087
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $1.15万
    • 财政年份:
      1998
    • 负责人:
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    • 依托单位:
    海外基金