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LAPTM4B基因多态性与肺癌易感性的关系
引用本文:邓丽娟,张青云,刘波,周柔丽.LAPTM4B基因多态性与肺癌易感性的关系[J].北京大学学报(医学版),2005,37(3):302-305.
作者姓名:邓丽娟  张青云  刘波  周柔丽
作者单位:1. 北京大学临床肿瘤学院,北京肿瘤医院,免疫研究室,北京,100036
2. 北京大学临床肿瘤学院,北京肿瘤医院,免疫研究室,北京,100036;北京大学临床肿瘤学院,北京肿瘤医院,检验科
3. 北京大学临床肿瘤学院,北京肿瘤医院,检验科
4. 北京大学临床肿瘤学院,北京肿瘤医院,北京大学基础医学院细胞生物学系
摘    要:目的:探讨溶酶体相关4次跨膜蛋白质β(lysosome-associated protein transmembrane4 beta,LAPTM4B)基因多态性与肺癌易感性的关系.方法:以病例-对照研究的方法,用基于特异性引物的PCR对134例正常人和162例肺癌患者进行LAPTM4B基因分型,将卡方检验用于检测肺癌组和对照组基因型频率和其它参数的分布.结果:LAPTM4B的*2等位基因频率在肺癌组中为40.1%,较对照组(28.0%)显著增高(P=0.002).基因型分布在肺癌组和对照组间差异有统计学意义.*1/2和*2/2基因携带者患肺癌的危险性分别是*1/1的1.91倍(95%CI:1.178~3.110)与3.26倍(95%CI:1.338~7.929).LAPTM4B基因型分布与患者年龄,肺癌的病理类型,分化程度,临床分期以及HBV感染等无明显关系.结论:LAPTM4B基因多态性与肺癌易感性相关,* 2等位基因可能是肺癌发生的危险因素.

关 键 词:肺肿瘤  病例对照研究  癌基因蛋白质类  多态现象(遗传学)  基因多态性  癌易感性  关系  lung  cancer  susceptibility  gene  polymorphism  危险因素  癌发生  等位基因  相关  感染  临床分期  分化程度  病理类型  患者年龄  危险性  基因携带者  统计学意义  组间差异  基因型分布
文章编号:1671-167X(2005)03-0302-04
修稿时间:2005年2月28日

Relationship between LAPTM4B gene polymorphism and susceptibility of lung cancer
DENG Li-juan,ZHANG Qing-yun,LIU Bo,ZHOU Rou-li.Relationship between LAPTM4B gene polymorphism and susceptibility of lung cancer[J].Journal of Peking University:Health Sciences,2005,37(3):302-305.
Authors:DENG Li-juan  ZHANG Qing-yun  LIU Bo  ZHOU Rou-li
Institution:Department of Immunology, Peking University School of Oncology, Beijing Cancer Hospital, Beijing 100036, China.
Abstract:OBJECTIVE: To investigate the possible association between the allelic variation of LAPTM4B and the genetic susceptibility of lung cancer. METHODS: The genotype of LAPTM4B was analyzed in 134 unrelated healthy adult individuals and 166 patients with lung cancer by utilizing polymerase chain reaction based on special primers. The genotypical distribution of LAPTM4B was analyzed by chi2 test. RESULTS: The allelic frequencies of the *2 were 40.1% and 28.0% in the lung cancer group and the healthy control group respectively, which was significantly different between the two groups (P=0.002). There was a significant difference in the overall genotypical distribution between the patients and the controls (P=0.005). The risk of suffering from lung cancer was increased 1.91 times in the individuals of the *1/2 genotype (95%CI: 1.178-3.110) and 3.26 times in the individuals of the *2/2 genotype of LAPTM4B (95%CI: 1.338-7.929) compared with the *1/2 genotype. No association was observed between the genotypical distribution of LAPTM4B and the clinical information on patients of lung cancer such as gender, age, pathological type, differentiation classification of TNM and infection of HBV. CONCLUSION: This study suggests that the allele *2 of LAPTM4B might be the risk factor of lung cancer, which could be associated with genetic susceptibility of lung cancer.
Keywords:Lung neoplasms  Case-control studies  Oncogene proteins  Polymorphism(Genetics)
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