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Association between polymorphisms of MIR17HG and risk of colorectal cancer in the Chinese Han population

机译:MIR17HG多态性与中国汉族人群中结直肠癌风险的关系

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Background Colorectal cancer is the third most common cancer worldwide. Recently, an increasing number of evidences suggest that genetic susceptibility plays an important role in the occurrence of colorectal cancer. This study aimed to better understand the influence of MIR17HG polymorphisms on colorectal cancer susceptibility in the Chinese Han population. Methods We recruited 514 patients with colorectal cancer and 510 healthy controls to investigate the association between polymorphisms of MIR17HG and risk of colorectal cancer in the Chinese Han population. Genotyping was performed with the Agena MassARRAY platform. We used the χ 2 test to compare the distributions of single nucleotide polymorphisms (SNPs) allele and genotypes frequencies between cases and controls. Odds ratios and 95% confidence intervals were calculated by logistic regression analysis to evaluate the association under genetic models. Linkage disequilibrium between the five SNPs was assessed using the Haploview software. Results Overall analysis found that rs7336610 and rs1428 and haplotype CTAGA were significantly associated with increased risk of colorectal cancer. However, we found rs7318578 was associated with a decreased risk of colorectal cancer in the dominant model. Stratification analysis showed that rs7336610, rs7318578, and rs1428 were also associated with rectal cancer risk. Gender stratification analysis found that rs7336610, rs7318578, rs17735387, and rs1428 were significantly associated with colorectal cancer risk in males. Conclusion In conclusion, this study indicated that the polymorphisms of MIR17HG were associated with colorectal cancer risk. Therefore, our findings may provide new insights into the development of colorectal cancer. Further association and functional studies are of great importance to confirm these results and to define the potential biological mechanism of colorectal cancer.
机译:背景背肠癌是全世界第三次常见的癌症。最近,越来越多的证据表明遗传易感性在结直肠癌的发生中起重要作用。本研究旨在更好地了解MiR17HG多态性对中国汉族人群结肠直肠癌易感性的影响。方法招聘了514例结直肠癌患者和510例健康对照,探讨了MIR17HG多态性与中国汉族人群结肠直肠癌的关系。基因分型用Agena Massarray平台进行。我们使用了χ2检验来比较单一核苷酸多态性(SNP)等位基因(SNP)等位基因和基因型频率之间的分布和对照。通过Logistic回归分析来计算差距比率和95%的置信区间,以评估遗传模型下的关联。使用HAPLOVIEW软件评估五个SNP之间的联动不平衡。结果总体分析发现,RS7336610和RS1428和单倍型CTAGA显着与成直肠癌的风险增加显着相关。然而,我们发现RS7318578与显性模型中的结肠直肠癌的风险降低有关。分层分析表明,RS7336610,RS7318578和RS1428也与直肠癌风险有关。性别分层分析发现,RS7336610,RS7318578,RS17735387和RS1428与男性结肠直肠癌风险显着相关。结论总之,本研究表明,MiR17Hg的多态性与结直肠癌风险有关。因此,我们的研究结果可能会对结直肠癌的发展提供新的见解。进一步的关联和功能性研究非常重视确认这些结果并确定结直肠癌的潜在生物学机制。

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