中山醫學大學機構典藏 CSMUIR:Item 310902500/3646
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 17938/22957 (78%)
造访人次 : 7404051      在线人数 : 162
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜寻范围 查询小技巧:
  • 您可在西文检索词汇前后加上"双引号",以获取较精准的检索结果
  • 若欲以作者姓名搜寻,建议至进阶搜寻限定作者字段,可获得较完整数据
  • 进阶搜寻


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: https://ir.csmu.edu.tw:8080/ir/handle/310902500/3646


    题名: Association of EcoRI Polymorphism of the Metastasis-Suppressor Gene NME1 with Susceptibility to and Severity of Non-Small Cell Lung Cancer
    作者: Yih-Shou Hsieh;Yao-Ling Lee;Shun-Fa Yang;Jia-Sin Yang;Wei Chen;Shuo-Chueh Chen;Chuen-Ming Shih
    贡献者: 中山醫學大學:醫學檢驗暨生物技術學系
    关键词: Lung cancer;EcoRI polymorphism;Metastasis-suppressor;NME1
    日期: 2007
    上传时间: 2011-03-22T08:25:13Z (UTC)
    ISSN: 0169-5002
    摘要: Human lung cancer cells with high metastatic potential show reduced expression of the metastasis-suppressor gene NME1. However, the biallelic EcoRI polymorphism of this gene has not been studied in lung cancer. With this allelic association study, we aimed to investigate the impact of polymorphisms of the NME1 gene on the susceptibility to and severity of non-small cell lung cancer (NSCLC).

    Methods
    Through a case-control study design, genomic DNA samples of 255 NSCLC patients and 303 controls, who were age and sex-matched and recruited from the health check-up unit, were subjected to polymorphism analysis with polymerase chain reaction-restriction fragment length polymorphism technique. The validity of this technique was proven by direct sequencing of polymerase chain reaction products. Statistical analyses were conducted to explore the contribution of polymorphism of the metastasis-suppressor gene NME1 in the susceptibility to and severity of NSCLC.

    Results
    Overall, the genotype frequencies of NME1 gene were significantly different between lung cancer patients and controls (p < 0.0001), and also different between patients with lung cancers of various stages (p < 0.0001). Logistic regression analysis revealed that higher odds ratios (ORs) for lung cancer were seen in patients homozygous (+/+) for variant allele (an OR of 4.02, 95% CI 2.39–6.76; p < 0.0001). Patients carrying a variant polymorphic homozygote (+/+) also had a tendency to advanced disease (p = 0.001).

    Conclusion
    A significant association between the polymorphisms of NME1 gene and the susceptibility to and severity of lung cancer was demonstrated.
    URI: https://ir.csmu.edu.tw:8080/handle/310902500/3646
    http://dx.doi.org/10.1016/j.lungcan.2007.06.008
    關聯: Lung Cancer,Volume 58, Issue 2, November 2007, Pages 191-195
    显示于类别:[醫學檢驗暨生物技術學系暨碩士班] 期刊論文

    文件中的档案:

    档案 描述 大小格式浏览次数
    index.html0KbHTML289检视/开启


    SFX Query

    在CSMUIR中所有的数据项都受到原著作权保护.

    TAIR相关文章

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回馈