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Genetic polymorphisms in the TERT-CLPTM1L region and lung cancer susceptibility in Chinese males

机译:中国雄性Try-Clptm1L区的遗传多态性和肺癌易感性

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The objective of the present study was to analyze the relationship between genetic polymorphisms of the rs2736098 locus of the telomerase reverse transcriptase (TERT) gene and the rs401681 locus of the cleft lip and palate transmembrane protein 1 (CLPTM1L) gene and the risk of developing lung cancer in males in Jinzhou. A total of 214 lung cancer patients who were admitted in Jinzhou Medical University were analyzed, and 216 healthy males were selected as controls. Venous blood from all subjects and data on relevant risk factors were collected. DNA was extracted from peripheral blood by the phenol-chloroform method. Real-time fluorescent quantitative PCR (TaqMan real-time PCR) was used for DNA amplification. The genotyping results of the genetic polymorphisms of the TERT rs2736098 and CLPTM1L rs401681 loci were detected. The risk of developing lung cancer in the population with the TERT rs2736098 locus carrying the T allele was 1.614 times that with the TERT rs2736098 locus carrying the C allele after adjustment of the age factor. The risk of developing lung cancer in the population carrying the TT mutant genotype and the CT genotype increased significantly compared with that carrying the CC wild genotype [odds ratio (OR)=1.815, 95% CI=1.132-2.957; OR=2.417, 95% CI=1.158-4.943]. Based on a comparison between the combination of the two mutant genotypes (CT+TT) and the wild homozygous genotype (CC), the mutant genotype increased the risk of developing lung cancer (OR=1.955, 95% CI=1.213-3.157). The risk of developing lung cancer in the population with the CLPTM1L rs401681 locus carrying the T allele was 1.399 times that carrying the C allele (OR=1.343, 95% CI=1.035-1.978). The population with the TERT rs2736098 locus carrying the mutant genotype (CT+TT) was associated with the number of tumors (OR=0.553, 95% CI=0.236-0.928). In conclusion, in males, the TERT rs2736098 and CLPTM1L rs401681 T alleles are the susceptibility factors for developing lung cancer. Individuals, including the smoking population, who carry both the TERT rs2736098 and CLPTM1L rs401681 T alleles are more likely to develop lung cancer.
机译:本研究的目的是分析端粒酶逆转录酶(TERT)基因的RS2736098基因座的遗传多态性与裂隙唇和腭跨膜蛋白1(CLPTM1L)基因的RS401681基因座之间的关系以及发育肺的风险锦州雄性癌症。分析了锦州医科大学入学的214名肺癌患者,并选择了216名健康的男性作为对照。收集了来自所有受试者和相关风险因素数据的静脉血。通过苯酚 - 氯仿方法从外周血中提取DNA。实时荧光定量PCR(Taqman实时PCR)用于DNA扩增。检测到TRES2736098和CLPTM1L RS401681基因座的遗传多态性的基因分型结果。携带T等位基因的TRY RS2736098基因座的人群中肺癌的风险为1.614倍,在调整年龄因子后携带C等位基因的TERT RS2736098基因座。与携带CC野生基因型(OR)= 1.815,95%CI = 1.132-2.957;或= 2.417,95%CI = 1.158-4.943]。基于两个突变基因型(CT + TT)和野生纯合基因型(CC)的组合之间的比较,突变基因型增加了肺癌(或= 1.955,95%CI = 1.213-3.157)的风险。携带T等位基因的CLPTM1L RS401681基因座的肺癌在群体中发育肺癌的风险为1.399倍,携带C等位基因(或= 1.343,95%CI = 1.035-1.978)。具有突变基因型(CT + TT)的TRET RS2736098基因座的人口与肿瘤的数量(或= 0.553,95%CI = 0.236-0.928)相关。总之,在雄性中,TRET RS2736098和CLPTM1L RS401681 T等位基因是肺癌的敏感因素。包括吸烟人口的个人,携带TERT RS2736098和CLPTM1L RS401681 T等位基因更有可能发展肺癌。

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