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KRAS和VEGF基因3'-非翻译区单核苷酸多态性预测结直肠癌易感性。

KRAS and VEGF gene 3'-UTR single nucleotide polymorphisms predicted susceptibility in colorectal cancer.

作者信息

Yang Minnan, Xiao Xiuli, Xing Xiaorui, Li Xin, Xia Tian, Long Hanan

机构信息

College of Preclinical Medicine, Southwest Medical University, Luzhou, Sichuan, China.

Department of Pathology, the Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.

出版信息

PLoS One. 2017 Mar 22;12(3):e0174140. doi: 10.1371/journal.pone.0174140. eCollection 2017.

Abstract

Single nucleotide polymorphisms (SNPs) in tumor-related genes have been reported to play important roles in cancer development. Recent studies have shown that 3'-untranslated regions (UTR) polymorphisms are associated with the occurrence and prognosis of cancers. The aim of this study is to analyze the association between KRAS and VEGF gene 3'-UTR SNPs and genetic susceptibility to colorectal cancer (CRC). In this case-control study of 371 CRC cases and 246 healthy controls, we analyzed the association between one SNP (rs1137188G > A) in the KRAS gene and four SNPs (rs3025039C > T, rs3025040C > T, rs3025053G > A and rs10434A > G) in the VEGF gene and CRC susceptibility by the improved multiplex ligase detection reaction (iMLDR) method. We checked the selected SNPs' minor allele frequency and its distribution in the frequency of Chinese people by Hap-map database and Hardy-Weinberg equilibrium, and used multivariate logistic regression models to estimate adjusted odds ratios (AORs) and 95% confidence intervals (95% CIs). We found that the rs3025039C variant genotype in the VEGF gene was associated with a significant protection for CRC (AOR = 0.693, 95% CI = 0.485-0.989; P = 0.043 for CC and CT+TT). Nevertheless, the difference was no longer significant after Bonferroni correction (Bonferroni-adjusted P = 0.172). In genetic polymorphisms analysis, we found that the KRAS rs1137188 variant AA genotype had higher portion of tumor size (≥ 5 cm) (P = 0.01; Bonferroni-adjusted P = 0.04), which suggested that the rs1137188 variant AA genotype may significantly be associated with increased progression of CRC. In conclusion, our study suggested that these five SNPs in the KRAS gene and the VEGF gene were not associated with CRC susceptibility in Han Chinese in Sichuan province.

摘要

据报道,肿瘤相关基因中的单核苷酸多态性(SNP)在癌症发展中起重要作用。最近的研究表明,3'-非翻译区(UTR)多态性与癌症的发生和预后相关。本研究的目的是分析KRAS和VEGF基因3'-UTR SNP与结直肠癌(CRC)遗传易感性之间的关联。在这项包含371例CRC病例和246例健康对照的病例对照研究中,我们采用改进的多重连接酶检测反应(iMLDR)方法分析了KRAS基因中的一个SNP(rs1137188G>A)和VEGF基因中的四个SNP(rs3025039C>T、rs3025040C>T、rs3025053G>A和rs10434A>G)与CRC易感性之间的关联。我们通过Hap-map数据库和哈迪-温伯格平衡检查所选SNP的次要等位基因频率及其在中国人群中的频率分布,并使用多因素逻辑回归模型估计调整后的比值比(AOR)和95%置信区间(95%CI)。我们发现,VEGF基因中的rs3025039C变异基因型对CRC具有显著的保护作用(AOR=0.693,95%CI=0.485-0.989;CC与CT+TT比较,P=0.043)。然而,经Bonferroni校正后差异不再显著(Bonferroni校正P=0.172)。在基因多态性分析中,我们发现KRAS rs1137188变异AA基因型的肿瘤大小(≥5cm)比例更高(P=0.01;Bonferroni校正P=0.04),这表明rs1137188变异AA基因型可能与CRC进展增加显著相关。总之,我们的研究表明,KRAS基因和VEGF基因中的这五个SNP与四川省汉族人群的CRC易感性无关。

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