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Single Nucleotide Polymorphisms of XRCC1 and the Risk of Head and Neck Cancer

机译:XRCC1 的单核苷酸多态性与头颈癌的风险

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Head and Neck Cancers (HNCs) accounts for more than 550,000 cases and 380,000 deaths annually, worldwide. Overall, 57.5% of global HNCs occur in Asia especially in India in both sexes. Single Nucleotide Polymorphisms (SNPs) of DNA repair genes in cancer are the most common form of genetic variations found in the human population.Aim: To draw an association, if any, between polymorphic 347 bp and 445 bp variants of XRCC1 gene and the risk of HNC in a Southern Indian population.Materials and Methods: In the present case-control study, 120 HNC cases were selected from the Department of Radiotherapy, Government General Hospital, Guntur, India. Characteristics were considered for risk assessment in 120 (76 male and 44 female) HNC Cases and XRCC1 gene single nucleotide polymorphisms (SNPs) were analysed in 30 HNC cases (random sampling) and 30 healthy subjects (controls, not habituated to alcohol and/or smoking) to compare the frequency of polymorph variants. DNA was isolated from peripheral blood and after DNA extraction SNPs were genotyped by direct sequencing. Deviations from the Hard-Weinberg Equilibrium (HWE) were tested by using online calculator, chi-square test was used to compare between two variables.Results: In the present study, out of 120 cases, 76 (63.33%) were males and 44 (36.66%) were females. About 72 (60%) cases of males had the habit of smoking and only 7 (15.91%) cases of females were smokers. Among male cases alone, 75.50% constitute smokers. A total of 57 cases, consisting of 18 (23.68%) males and majority of females 39 (88.63%) responded that they never consumed alcohol. In the present study, data showed no significant allelic associations for SNP of XRCC1 347bp/445bp and HNC.Conclusion: The present study confirms the principle role of cigarette smoking and alcohol consumption in HNC. This is significant and positive interaction between these two factors. The frequency of heterozygous genotype (A/G) of XRCC1 gene in both cases and controls showed no significant difference and hence, There was no association between them. In addition, further studies are required for evaluating the effect of gene to gene and gene to environment interactions on these gene polymorphisms with HNC susceptibility, in Indian population.
机译:全世界每年头颈癌(HNC)占55万多例,死亡38万例。总体而言,全球HNC的57.5%发生在亚洲,尤其是印度的男女。 DNA修复基因在癌症中的单核苷酸多态性(SNP)是人类人群中最常见的遗传变异形式。目的:找出XRCC1基因的多态性347 bp和445 bp变异之间的关联(如果有)。 材料与方法:在本病例对照研究中,从印度古图尔政府总医院放射治疗科中选出120例HNC病例。在120例HNC病例(76例男性和44例女性)中考虑了特征进行风险评估,并在30例HNC病例(随机抽样)和30例健康受试者(对照组,不习惯饮酒和/或饮酒)中分析了XRCC1基因单核苷酸多态性(SNP)。吸烟)以比较多态变体的频率。从外周血中分离DNA,提取DNA后,通过直接测序对SNP进行基因分型。使用在线计算器测试与Hard-Weinberg平衡(HWE)的偏差,使用卡方检验比较两个变量。结果:在本研究中,在120例病例中,有76例(63.33%)男性和女性分别为44和36.66%。大约72(60%)例男性有吸烟习惯,只有7(15.91%)例女性为吸烟者。仅男性病例中,吸烟者占75.50%。共有57例病例,其中男性18例(23.68%),女性39例多数(88.63%)回答他们从不饮酒。在本研究中,数据显示XRCC1 347bp / 445bp的SNP与HNC没有明显的等位基因相关性。结论:本研究证实了吸烟和饮酒在HNC中的主要作用。这两个因素之间是显着且积极的相互作用。 XRCC1基因的杂合基因型(A / G)的频率在两个病例和对照中均无显着差异,因此两者之间没有关联。另外,在印度人群中,需要进一步的研究来评估基因与基因以及基因与环境之间的相互作用对这些具有HNC敏感性的基因多态性的影响。

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