唐文军, 闫其星, 王天柱, 易国辉, 薛丽, 林海锋. TP63 rs6790167多态性与海南汉族人肺癌的相关性研究[J]. 中国肿瘤临床, 2017, 44(21): 1061-1066. DOI: 10.3969/j.issn.1000-8179.2017.21.400
引用本文: 唐文军, 闫其星, 王天柱, 易国辉, 薛丽, 林海锋. TP63 rs6790167多态性与海南汉族人肺癌的相关性研究[J]. 中国肿瘤临床, 2017, 44(21): 1061-1066. DOI: 10.3969/j.issn.1000-8179.2017.21.400
TANG Wenjun, YAN Qixing, WANG Tianzhu, GUO Huiyi, XUE Li, LIN Haifeng. Association of the polymorphisms in TP63 rs6790167 with risk for lung cancer in Hainan Han population[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2017, 44(21): 1061-1066. DOI: 10.3969/j.issn.1000-8179.2017.21.400
Citation: TANG Wenjun, YAN Qixing, WANG Tianzhu, GUO Huiyi, XUE Li, LIN Haifeng. Association of the polymorphisms in TP63 rs6790167 with risk for lung cancer in Hainan Han population[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2017, 44(21): 1061-1066. DOI: 10.3969/j.issn.1000-8179.2017.21.400

TP63 rs6790167多态性与海南汉族人肺癌的相关性研究

Association of the polymorphisms in TP63 rs6790167 with risk for lung cancer in Hainan Han population

  • 摘要:
      目的  探讨TP63 rs6790167多态性与海南汉族人肺癌之间的相关性。
      方法  收集2014年6月至2015年7月258例海南医学院第二附属医院就诊的肺癌患者和270例健康对照者的外周静脉血,采用病例对照研究的方法,提取血液基因组DNA,应用等位基因特异性聚合酶链反应(allele-specific PCR,AS-PCR)法检测肺癌组和对照组人群的TP63 rs6790167位点的多态基因型。
      结果  肺癌组中TP63 rs6790167位点的G等位基因分布频率明显高于对照组(P=0.045)。进一步分层分析显示,在肺腺癌组中,非吸烟男性的GG基因型分布和G等位基因的分布频率均显著高于对照组(P < 0.001,P=0.001),携带GG基因型的非吸烟男性的肺腺癌发病风险与AA基因型相比明显升高(OR=6.66,95%CI为2.16~20.41),相对于TP63 rs6790167位点的A等位基因,携带G等位基因的非吸烟男性的肺腺癌发病风险显著增加(OR=2.54,95%CI为1.42~4.56)。
      结论  TP63 rs6790167多态性与肺腺癌的发生有关,对非吸烟男性人群肺腺癌的发生可能具有预测作用。

     

    Abstract:
      Objective  To evaluate the association between the polymorphisms in TP63 rs6790167 and lung cancer.
      Methods  We performed a case-control study with 258 patients and 270 controls. Genomic DNA was extracted using a blood genome extraction kit. Genotyping was conducted using allele-specific polymerase chain reaction (AS-PCR).
      Results  No significant difference was observed in the genotype of TP63 rs6790167 between cases and controls, and allele frequencies significantly elevated in the cases (P=0.045). In a further stratified analysis by gender and smoking status, the frequencies of the GG genotype and G allele of rs6790167 were significantly higher in non-smoking male patients with lung adenocarcinoma (P=0.000, P=0.001), individuals with GG genotype had a higher risk for lung adenocarcinoma in non-smoking man (OR=6.66, 95% CI: 2.16-20.41). Individuals with G allele had a higher risk for lung adenocarcinoma in a non-smoking man (OR=2.54, 95% CI: 1.42-4.56) in comparison with individuals with A allele.
      Conclusion  We found that the polymorphisms of TP63 rs6790167 were associated with the risk for lung adenocarcinoma in non-smoking men and that these polymorphisms may be a predictor for lung adenocarcinoma in non-smoking men.

     

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