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Polymorphisms in tumor necrosis factor genes and susceptibility to esophageal squamous cell carcinoma and gastric cardiac adenocarcinoma in a population of high incidence region of North China

机译:华北高发区人群肿瘤坏死因子基因多态性与食管鳞状细胞癌和胃cardiac门腺癌的易感性

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Background We investigated the possible association of the functional polymorphisms in the tumor necrosis factor (TNF) genes with susceptibility to esophageal squamous cell carcinoma (ESCC) and gastric cardiac adenocarcinoma (GCA). Methods The TNF-α - 308G/A and TNF-β + 252G/A single nucleotide polymorphisms ( SNPs) were genotyped using polymerase-chain reaction-restriction fragment length polymorphism ( PCR-RFLP) analysis, in 555 cancer patients (291 ESCC and 264 GCA) and 437 healthy controls in a high incidence region of North China. Results Among healthy controls, frequencies of the TNF-α 1/1, 1/2 and 2/2 genotypes were 89. 4% ,9. 2% and 1. 4% respectively, while frequencies of the TNF-β B1/B1, B1/B2 and B2/B2 genotypes were 12. 6% , 32.3% and 55. 1% , respectively. No significant difference was found in the overall genotype and allelotype distribution of the TNF-α -308G/A and TNF-β +252G/A SNPs among cancer patients and controls. However, both the B1/B1 genotype and B1/B2 genotype significantly increased the risk of developing ESCC [the age and gender adjusted odds ratio (OR) = 2. 04 and 1. 91, 95% confidence interval ( CI) = 1. 04 -4. 43 and 1. 14 -2. 60, respectively] and GCA (the age and gender adjusted OR -2. 68 and 2. 64, 95% CI = 1. 14 -6. 29 and 1. 47 -4. 72, respectively) in individuals with negative family history of UGIC, in comparison with the B2/B2 genotype. When the two TNF polymorphisms were combined and analyzed, individuals with the TNF-β B1/B2 and TNF-α1/2 or 2/2 genotypes significantly reduced the risk of developing ESCC and GCA, in comparison with those harboring the TNF-β B2/B2 and TNF-α 1/1 genotypes (the age and gender adjusted OR = 0. 37 and 0. 34, 95% CI =0. 15 -0. 92 and 0. 13 -0. 90, respectively). Conclusions Therefore, the TNF-α - 308G/A and TNF-β + 252G/A genotyping may be used as a stratification markers to predicate the risk of ESCC and GCA development in North China.
机译:背景我们研究了肿瘤坏死因子(TNF)基因功能多态性与食管鳞状细胞癌(ESCC)和胃cardiac门腺癌(GCA)易感性的关系。方法采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析法对555例癌症患者(291例ESCC和2例)中的TNF-α-308G/ A和TNF-β+ 252G / A单核苷酸多态性(SNP)进行基因分型。 264 GCA)和437个健康对照在华北高发地区。结果在健康对照组中,TNF-α1 / 1、1 / 2和2/2基因型的频率为89. 4%,9。 TNF-βB1 / B1,B1 / B2和B2 / B2基因型的频率分别为2%和1. 4%,分别为12.6%,32.3%和55.1%。在癌症患者和对照组中,TNF-α-308G / A和TNF-β+ 252G / A SNP的总体基因型和等位基因分布没有显着差异。但是,B1 / B1基因型和B1 / B2基因型均显着增加了发生ESCC的风险[年龄和性别调整后的优势比(OR)=2。04和1。91,95%置信区间(CI)= 1。 04 -4。 43和1. 14 -2。 60岁]和GCA(年龄和性别调整后的OR -2。68和2. 64,95%CI分别为1. 14 -6。29和1. 47 -4。72)在家族史为阴性的个体中与B2 / B2基因型比较。结合两种TNF多态性并进行分析后,与携带TNF-βB2的个体相比,具有TNF-βB1 / B2和TNF-α1/ 2或2/2基因型的个体显着降低了产生ESCC和GCA的风险。 / B2和TNF-α1/1基因型(年龄和性别调整后的OR分别为0. 37和0. 34,95%CI = 0。15 -0。92和0. 13 -0。90)。结论因此,TNF-α-308G / A和TNF-β+ 252G / A基因分型可作为分层标记,预测华北地区ESCC和GCA发生的风险。

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