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Gender-specific association of NFKBIA promoter polymorphisms with the risk of sporadic colorectal cancer

机译:性别相关的NFKBIA启动子多态性与散发性结直肠癌风险的关联

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The inhibitory protein IκBα, encoded by the NFKBIA gene, plays an important role in regulating the activity of nuclear factor-kappa B, a transcription factor which has been implicated in the initiation and progression of cancers. This study aimed to evaluate the association of NFKBIA -826C>T (rs2233406) and -881A>G (rs3138053) polymorphisms with the risk of sporadic colorectal cancer (CRC) in Malaysian population. A case-control study comprising 474 subjects (237 CRC patients and 237 cancer-free controls) was carried out. The polymorphisms were genotyped from the genomic DNA of the study subjects employing PCR-RFLP, followed by DNA sequencing. The association between the polymorphic genotypes and CRC risk was evaluated by deriving odds ratios (ORs) and 95 % confidence intervals (CIs) using unconditional logistic regression analysis. The two polymorphisms were in complete and perfect linkage disequilibrium (D′ = 1.0, r2 = 1.0). Overall, no statistically significant CRC risk association was found for the polymorphisms (P > 0.05). A similar lack of association was observed when the data were stratified according to ethnicity (P > 0.05). However, stratification by gender revealed a significant inverse association between the heterozygous genotype of the polymorphisms and the risk of CRC among females (OR 0.53, 95 % CI 0.29-0.97, P = 0.04), but not among males (P > 0.05). In conclusion, the heterozygous genotype of the polymorphisms could contribute to a significantly decreased CRC risk among females, but not males, in the Malaysian population.
机译:由NFKBIA基因编码的抑制蛋白IκBα在调节核因子-κB的活性中起着重要作用,核转录因子-κB已与癌症的发生和发展有关。这项研究旨在评估马来西亚人群中NFKBIA -826C> T(rs2233406)和-881A> G(rs3138053)多态性与散发性结直肠癌(CRC)风险的关系。进行了一项包括474名受试者(237名CRC患者和237名无癌对照)的病例对照研究。使用PCR-RFLP从研究对象的基因组DNA对基因多态性进行基因分型,然后进行DNA测序。通过使用无条件逻辑回归分析得出比值比(OR)和95%置信区间(CI),评估了多态性基因型与CRC风险之间的关联。这两个多态性处于完全和完美的连锁不平衡状态(D'= 1.0,r2 = 1.0)。总体而言,未发现该多态性的统计学上显着的CRC风险关联(P> 0.05)。当根据种族对数据进行分层时,也观察到类似的关联性缺失(P> 0.05)。然而,按性别分层显示,女性多态性的杂合基因型与CRC风险之间存在显着的负相关关系(OR 0.53,95%CI 0.29-0.97,P = 0.04),而男性之间则没有(P> 0.05)。总之,多态性的杂合基因型可能导致马来西亚人群中女性(而非男性)的CRC风险显着降低。

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