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Tumor necrosis factor-alpha gene promoter -308 and -238 polymorphisms in patients with lung cancer as a second primary tumor

机译:肺癌为第二原发肿瘤患者的肿瘤坏死因子-α基因启动子-308和-238多态性

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Background Lung cancer is the most common second primary cancer. We investigated whether the TNF-alpha-308 and TNF-alpha-238 polymorphisms were associated with the susceptibility and severity of lung cancer as the second primary cancer (LC2). Material and Methods This study included 104 patients from the group LC2. The control subjects included 2 groups. The first control group (LC1) comprised 201 unrelated patients with lung cancer as a first primary cancer. The second control group (HC) comprised 230 healthy blood donors, matched for sex and age to the study group. Results The frequencies of the TNF-alpha-238 polymorphism GG genotype and the G allele were higher in the LC2 group than in the LC1 group, but the differences did not reach significance (p=0.054 and p=0.057, respectively). Similar differences were found in the TNF-alpha-238 polymorphism GG genotype and G allele between the LC2 group and the HC group (p=0.054 and p=0.057, respectively). In terms of the different types of lung cancer, patients with a second primary NSCLC (non-small cell lung cancer) more frequently had TNF-alpha-238 polymorphism GG genotypes and G alleles than patients with a first primary NSCLC (the differences approached statistical significance: p=0.060, p=0.064, respectively). All (100%) patients of group LC2 (n=104) had the GG genotype and the G allele. GG genotype was exclusive and no A allele was found in group LC2. Conclusions TNF-alpha-238 polymorphism GG genotype and the G allele could have a promotional effect on the development of NSCLC in the group of patients with LC2.
机译:背景技术肺癌是最常见的第二原发癌。我们调查了TNF-alpha-308和TNF-alpha-238多态性是否与作为第二原发癌(LC2)的肺癌的易感性和严重性相关。材料和方法该研究纳入了来自LC2组的104名患者。对照组包括2组。第一对照组(LC1)包括201名无关的肺癌患者,作为第一原发癌。第二对照组(HC)包括230名健康献血者,其性别和年龄与研究组相匹配。结果LC2组的TNF-α-238基因多态性GG基因型频率和G等位基因频率高于LC1组,但差异无统计学意义(分别为p = 0.054和p = 0.057)。 LC2组和HC组之间的TNF-α-238基因多态性GG基因型和G等位基因存在相似的差异(分别为p = 0.054和p = 0.057)。就肺癌的不同类型而言,第二个原发性NSCLC(非小细胞肺癌)患者比第一个原发性NSCLC患者更常见TNF-α-238多态性GG基因型和G等位基因(差异接近统计学上的差异)显着性:分别为p = 0.060,p = 0.064)。 LC2组(n = 104)的所有患者(100%)均具有GG基因型和G等位基因。 GG基因型是排他性的,在LC2组中未发现A等位基因。结论TNF-α-238基因多态性GG基因型和G等位基因可能对LC2组NSCLC的发生有促进作用。

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