Suppression of metastasis due to regulation of PETA3/CD151

通过 PETA3/CD151 的调节抑制转移

基本信息

  • 批准号:
    12470280
  • 负责人:
  • 金额:
    $ 9.41万
  • 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:
    2000
  • 资助国家:
    日本
  • 起止时间:
    2000 至 2001
  • 项目状态:
    已结题

项目摘要

CD151 is identical to an exciting gene PETA-3 which may promote tumor metastasis of malignant cells and its expression may be involved in the malignant progression cancer. Previously, we found that MRP- 1/CD9, a member of the transmembrane 4 superfamily (TM4SF), suppressed cell motility and metastatic potential to lungs. Moreover, reduction of MRP-i/CD9 gene expression was found to be a factor of a poor prognosis for the patients with non-small cell lung cancer, as was another member of TM4SF, KAI1/CD82.On the basis of these results, we used RT-PCR and immunohistochemical technique for a retrospective study of GD15I gene expression in tumor tissues from 145 lung cancer patients ; 72 tumors were stage I, 29 stage II, 27 stage IIIA and 17 stage IIIB While 8 6 patients had the tumors with positive CD151 gene, 59 had the negative CD151 gene tumors. The overall survival rate of patients with CD151 positive tumors was much lower than that of CD151 negative patients (51.9% vs 73.1 % ; p=O.O13). Similarly, the overall survival rate of CD151 positive patients with adenocarcinoma was much lower than that of CD151 negative patients (47.4% vs 71.9% ; p=O.O47). Multivariate analysis with the Cox regression model indicated that CD151 positivity correlated best with the overall survival rate except lymph node status and tumor status. Our findings suggest that high CD151 gene expression in lung cancer may be associated with a poor prognosis. Assessment of CD151 could be instrumental for improvements in lung cancer diagnosis and therapies. In addition, we studied 146 colon cancer patients who underwent curative surgery. A significant relationship was found between PETA-3/CD151 expression and tumor status. Positive PETA-3/CD151 expression had a bad effect on the overall survival rate of patients with colon cancer (P = 0.022).
CD151与一个令人兴奋的基因PETA-3相同,可能促进恶性细胞的肿瘤转移,其表达可能参与肿瘤的恶性进展。先前,我们发现MRP- 1/CD9,跨膜4超家族(TM4SF)的成员,抑制细胞运动和肺转移潜能。此外,MRP-i/CD9基因表达降低是非小细胞肺癌患者预后不良的一个因素,TM4SF的另一个成员KAI1/CD82也是如此。在此基础上,我们采用RT-PCR和免疫组织化学技术对145例肺癌患者肿瘤组织中GD15I基因的表达进行回顾性研究;其中I期72例,II期29例,IIIA期27例,IIIB期17例,CD151基因阳性肿瘤86例,CD151基因阴性肿瘤59例。CD151阳性肿瘤患者的总生存率明显低于CD151阴性肿瘤患者(51.9% vs 73.1%; p= 0.13)。同样,CD151阳性腺癌患者的总生存率远低于CD151阴性患者(47.4% vs 71.9%; p= 0.47)。Cox回归模型多因素分析显示,除淋巴结状态和肿瘤状态外,CD151阳性与总生存率相关性最强。我们的研究结果表明,CD151基因在肺癌中的高表达可能与预后不良有关。CD151的评估可能有助于改善肺癌的诊断和治疗。此外,我们研究了146名接受治疗性手术的结肠癌患者。PETA-3/CD151的表达与肿瘤状态有显著关系。PETA-3/CD151阳性表达对结肠癌患者的总生存率有不良影响(P = 0.022)。

项目成果

期刊论文数量(58)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Yagita, M., et al.: "A novel natural killer cell line (KHYG-1) from a patient with aggressive natural killer cell leukemia carrying a p53 point mutation"Leukemia. 14. 922-930 (2000)
Yagita, M. 等人:“一种新型自然杀伤细胞系 (KHYG-1),来自携带 p53 点突变的侵袭性自然杀伤细胞白血病患者”白血病。
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    0
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Hashida H, et al.: "Integrin α3 Expression as a Prognostic Factor in Colon Cancer : Association with MRP-1/CD9 and KAI1/CD82"Int.J.Cancer. 97. 518-525 (2002)
Hashida H 等人:“整合素 α3 表达作为结肠癌的预后因素:与 MRP-1/CD9 和 KAI1/CD82 的关联”Int.J.Cancer. 97. 518-525 (2002)
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    0
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Tokuhara, T., et al.: "Clinical sibnificance of CD151 gene expression in non-small cell lung cancer"Clinical Cancer Research. 7. 4109-4114 (2001)
Tokuhara, T. 等人:“CD151 基因表达在非小细胞肺癌中的临床意义”临床癌症研究。
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    0
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Kohno, M., et al.: "CD151 enhances cell motility and metastasis of cancer cells in the presence of focal adhesion kinase"International Journal of Cancer. 97. 336-343 (2002)
Kohno, M., 等人:“CD151 在粘着斑激酶存在下增强癌细胞的细胞运动和转移”国际癌症杂志。
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  • 影响因子:
    0
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  • 通讯作者:
Hashida H, et al.: "The Novel Monoclonal Antibody MH8-4 Inhibiting Cell Motility Recognizes Integrin α3 : Inverse of Its Expression with Metastases in Colon Cancer"Int.J.Oncol.. 18. 89-95 (2001)
Hashida H 等人:“新型单克隆抗体 MH8-4 抑制细胞运动识别整合素 α3:结肠癌转移中其表达的反转”Int.J.Oncol.. 18. 89-95 (2001)
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MIYAKE Masayuki其他文献

MIYAKE Masayuki的其他文献

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{{ truncateString('MIYAKE Masayuki', 18)}}的其他基金

Inhibition of metastasis and tetraspanin expression by the human monoclonal antibody directed to CD151 and RNA interference
CD151 人单克隆抗体和 RNA 干扰对转移和四跨膜蛋白表达的抑制
  • 批准号:
    19390369
  • 财政年份:
    2007
  • 资助金额:
    $ 9.41万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Analysis of the function of TM4SF complex and its application of lung cancer therapy.
TM4SF复合物的功能分析及其在肺癌治疗中的应用
  • 批准号:
    16390400
  • 财政年份:
    2004
  • 资助金额:
    $ 9.41万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Analysis of the function of TM4SF complex and lung cancer gene therapy based on using this complex.
TM4SF复合物的功能分析及基于该复合物的肺癌基因治疗。
  • 批准号:
    14370421
  • 财政年份:
    2002
  • 资助金额:
    $ 9.41万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Cancer Gene Therapy with Adenovirally or Immunogene TM4SF
使用腺病毒或免疫基因 TM4SF 进行癌症基因治疗
  • 批准号:
    10557115
  • 财政年份:
    1998
  • 资助金额:
    $ 9.41万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
The analysis of the function of TM4SF and the suppression of the cancer metastasis by its regulation
TM4SF的功能分析及其调节抑制癌症转移
  • 批准号:
    08407040
  • 财政年份:
    1996
  • 资助金额:
    $ 9.41万
  • 项目类别:
    Grant-in-Aid for Scientific Research (A)
Prospective study of the patients with cancer according to MRP-1/CD9 status and regulation of metastastasis of cancer by means of MRP-1/CD9 control
根据MRP-1/CD9状态对癌症患者进行前瞻性研究以及通过MRP-1/CD9控制调节癌症转移
  • 批准号:
    07557253
  • 财政年份:
    1995
  • 资助金额:
    $ 9.41万
  • 项目类别:
    Grant-in-Aid for Scientific Research (A)
Analysis of structure of MRP-1/CD9 mutation and regulation of metastasis of cancer by means of MRP-1/CD9 control
MRP-1/CD9突变结构分析及MRP-1/CD9调控癌症转移
  • 批准号:
    06454405
  • 财政年份:
    1994
  • 资助金额:
    $ 9.41万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (B)
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