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Genetic polymorphisms of superoxide dismutase-1 A251G and catalase C-262T with the risk of colorectal cancer

机译:超氧化物歧化酶-1A251G和过氧化氢酶C-262T的遗传多态性与大肠癌风险

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摘要

Oxidative stress is significant in numerous types of disease including cancer. To protect cells and organs against reactive oxygen species (ROS), the body has evolved an antioxidant protection system that involved in the detoxification of ROS. Single nucleotide polymorphisms (SNP) of anti-oxidative enzymes may dramatically change the activity of the encoded proteins; therefore, certain alleles can be established as risk factors for some kind of multi-factorial diseases including cancer. In present study we investigate the possible association between polymorphisms of superoxide dismutase 1 (SOD1, OMIM: 147450) and catalase (CAT, OMIM: 115500) genes and the risk of colorectal cancer (CRC). The study included 204 colorectal cancer patients and 239 healthy control group matched for gender and age. Genotyping of SOD1 A251G and CAT C-262T were done by polymerase chain reaction and restriction fragment length polymorphism (PCR-RFLP) method. There was no significant association between CAT C-262T polymorphism and susceptibility to CRC (P>0.05). The carries of the G allele of SOD1 significantly showed higher prevalence in CRC patients compared with the control group (OR=1.84, 95% CI=1.13-2.98, P=0.013). We assessed the effect of combination of genotypes of the study polymorphisms on the risk of CRC. We found that the combination of AG+GG (SOD1) and CC (CAT) increases the risk of developing CRC (OR=2.38, 95% CI=1.25-4.52, P=0.008).
机译:氧化应激在包括癌症在内的多种疾病中都很重要。为了保护细胞和器官免受活性氧(ROS)的侵害,人体进化出了一种抗氧化剂保护系统,该系统参与了ROS的解毒。抗氧化酶的单核苷酸多态性(SNP)可能会极大地改变编码蛋白的活性。因此,可以将某些等位基因确定为包括癌症在内的某种多因素疾病的危险因素。在本研究中,我们调查了超氧化物歧化酶1(SOD1,OMIM:147450)和过氧化氢酶(CAT,OMIM:115500)基因多态性与结直肠癌(CRC)风险之间的可能联系。该研究包括204位大肠癌患者和239名性别和年龄相匹配的健康对照组。通过聚合酶链反应和限制性片段长度多态性(PCR-RFLP)方法对SOD1 A251G和CAT C-262T进行基因分型。 CAT C-262T基因多态性与CRC易感性之间无显着相关性(P> 0.05)。与对照组相比,SOD1的G等位基因携带率显着高于CRC组(OR = 1.84,95%CI = 1.13-2.98,P = 0.013)。我们评估了研究多态性基因型组合对CRC风险的影响。我们发现AG + GG(SOD1)和CC(CAT)的组合会增加发生CRC的风险(OR = 2.38,95%CI = 1.25-4.52,P = 0.008)。

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