aurora 2 is related to lymph node metastasis in colon and gastric carcinoma

aurora 2与结肠癌和胃癌淋巴结转移相关

基本信息

  • 批准号:
    12671232
  • 负责人:
  • 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:
    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

Backgrounds: Aurora2 is a family of human serine/threonine kinases characterized as cell cycle regulators. In this study, we evaluated the expression of aurora 2 mRNA in gastro-intestinal carcinoma and the correlation between overexpression and clinico-pathological factors. Material and methods: We studied the 201 Japanese patients with carcinoma of gastrointestinal tract, including 53 esophageal cancer, 72 gastric cancer and 76 colorectal cancer. The expression of aurora 2 was investigated by RT-PCR. Results: Aurora 2 mRNA was expressed in 27 of 53 (51%) esophageal cancer, 38 of 72 (53%) gastric cancer and 36 of 76 (46%) colorectal cancer. The relations between the aurora2 expression and the clinicopathological factors was examined. In gastric carcinoma, lymph node metastasis was shown in 27 of 38 (71%) cases with aurora2 expression positive group, more frequent than those with negative expression (p<0.01). In colon carcinoma, lymph node metastasis was present in 23 of 36 (64%) cases with expression positive group and in 7 of 40 (18%) without, a statistically significant difference (p<0.01). There was lymphatic vessel invasion in 25 of 36 (69%) in the aurora2 expression positive group but in only 12 of 40 (30%) in the negative group (p<0.01). There was a significant differences between the two groups in Dukes classification (p<0.01). The overall 5-year survival rate for patients with aurora2 overexpression was lower than for patients without expression in colorectal cancer (92% vs. 64%, p<0.05). Conclusions: These results suggested that aurora2 expression was associated with tumor progression and patients survival and may be a new prognostic indicator for patients with colon carcinoma.
背景:Aurora2是一个人类丝氨酸/苏氨酸激酶家族,其特征是细胞周期调节因子。在本研究中,我们评估了极光2 mRNA在胃肠道肿瘤中的表达及其与临床病理因素的相关性。材料与方法:对201例日本胃肠道癌患者进行研究,其中食管癌53例,胃癌72例,结直肠癌76例。采用RT-PCR技术检测极光2的表达情况。结果:53例食管癌中27例(51%)、72例胃癌中38例(53%)、76例结直肠癌中36例(46%)表达了Aurora 2 mRNA。探讨aurora2表达与临床病理因素的关系。38例胃癌中,aurora2阳性表达组有27例(71%)出现淋巴结转移,高于阴性表达组(p<0.01)。在结肠癌中,表达阳性组36例中有23例(64%)出现淋巴结转移,未表达阳性组40例中有7例(18%)出现淋巴结转移,差异有统计学意义(p<0.01)。aurora2阳性表达组36例中有25例(69%)出现淋巴管侵犯,阴性表达组40例中仅有12例(30%)出现淋巴管侵犯(p<0.01)。两组间Dukes分型差异有统计学意义(p<0.01)。在结直肠癌中,aurora2过表达患者的总体5年生存率低于无表达患者(92% vs. 64%, p<0.05)。结论:这些结果提示,aurora2表达与肿瘤进展和患者生存相关,可能是结肠癌患者预后的新指标。

项目成果

期刊论文数量(22)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Mori M.et al.: "Absence of Msh2 protein expression is associated with alteration in the FHIT locus and Fhit protein expression in colorectal carcinoma"Cancer Res. 61. 7379-7382 (2001)
Mori M.等人:“Msh2 蛋白表达的缺失与结直肠癌中 FHIT 位点和 Fhit 蛋白表达的改变有关”Cancer Res。
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    0
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Tahara K. et al.: "MAGE-specific cytotoxic T lymphocytes require non-specific CD54 adherence receptors on carcinoma cells."Int J Oncol. 17. 805-810 (2000)
Tahara K. 等人:“MAGE 特异性细胞毒性 T 淋巴细胞需要癌细胞上的非特异性 CD54 粘附受体。”Int J Oncol。
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    0
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Mori M et al.: "Altered expression of Fhit in carcinoma and precarcinomatous lesions of the esophagus"Cancer Res.. 60・5. 1177-1182 (2000)
Mori M等:“食管癌和癌前病变中Fhit的表达改变”Cancer Res. 1177-1182 (2000)。
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    0
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Kataoka A. et al.: "RT-PCR detection of breast cancer cells in sentinellymph nodes."Int J Oncol. 16. 1147-1152 (2000)
Kataoka A. 等人:“RT-PCR 检测前哨淋巴结中的乳腺癌细胞。”Int J Oncol。
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  • 影响因子:
    0
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Matsuyama A et al: "Hepatoma-derived growth factor is associated witn reduced sensitivity to irradiation in esophageal cancer"Cancer Res. 61. 5714-5717 (2001)
Matsuyama A 等人:“肝癌衍生生长因子与食道癌对辐射的敏感性降低有关”Cancer Res。
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    0
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SADANAGA Noriaki其他文献

SADANAGA Noriaki的其他文献

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{{ truncateString('SADANAGA Noriaki', 18)}}的其他基金

New Molecular target of cancer cell migration in breast cancer patients.
乳腺癌患者癌细胞迁移的新分子靶点。
  • 批准号:
    19591510
  • 财政年份:
    2007
  • 资助金额:
    $ 2.18万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
pH regulating therapy for hepatocellular carcinoma
pH调节治疗肝细胞癌
  • 批准号:
    10671199
  • 财政年份:
    1998
  • 资助金额:
    $ 2.18万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)

相似海外基金

Novel human oncogene STK15/BTAK/Aurora 2
人类新癌基因 STK15/BTAK/Aurora 2
  • 批准号:
    6661168
  • 财政年份:
    2001
  • 资助金额:
    $ 2.18万
  • 项目类别:
Novel human oncogene STK15/BTAK/Aurora 2
人类新癌基因 STK15/BTAK/Aurora 2
  • 批准号:
    6794608
  • 财政年份:
    2001
  • 资助金额:
    $ 2.18万
  • 项目类别:
Novel human oncogene STK15/BTAK/Aurora 2
人类新癌基因 STK15/BTAK/Aurora 2
  • 批准号:
    6522641
  • 财政年份:
    2001
  • 资助金额:
    $ 2.18万
  • 项目类别:
Novel human oncogene STK15/BTAK/Aurora 2
人类新癌基因 STK15/BTAK/Aurora 2
  • 批准号:
    6383016
  • 财政年份:
    2001
  • 资助金额:
    $ 2.18万
  • 项目类别:
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