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Cyclooxygenase-2 Polymorphisms and Breast Cancer Associated Risk in Pakistani Patients

机译:巴基斯坦患者中环氧合酶2多态性与乳腺癌相关的风险

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Prostaglandins produced by Cyclooxygenase-2 enzyme have been implicated to have a role in breast carcinogenesis. Several single nucleotide polymorphisms (SNPs) linked to COX-2 enzyme are reported to modulate its expression. The aim of the present study was to examine association of these SNPs to breast cancer risk in Pakistani patients. Methods In this case-control study, three sequence variants rs689465, rs689466, rs20417 in the promoter region of COX-2 were screened to evaluate the association with breast cancer risk. A total of 150 breast cancer patients and 101 healthy control genomic DNA were genotyped for rs689456, rs689466, rs20417 and their genotypes distribution in cases and control were compared using Pearson chi square test. Risk association was analyzed through odd ratio calculated by logistic regression. Results A screening analysis of COX-2 SNPs in 101 healthy controls showed distribution of Minor allelic frequency distribution of SNPs as follows : rs689465 (0.12), rs689466 (0.15), rs20417 (0.23). Further analyses revealed that their observed genotype frequencies were consistent with Hardy Weinberg equilibrium and strong linkage disequilibrium was identified between rs20417, rs689465 and rs689466. The Combined allele variants analysis showed that Haplotype rs68965G- 689466A-20417C (OR 2.909; CI 95 %1.3776.327; P = 0.007) was significantly associated with breast cancer. Conclusions Our results indicate no strong association between three most frequent COX-2 SNPs rs689465 rs689466, rs20417 studied with breast cancer risk in the single locus analysis. However, our data suggested that combined COX-2 SNP haplotype have a role in breast cancer associated risk in Pakistani patients.
机译:已经暗示由环氧合酶2酶产生的前列腺素在乳腺癌的致癌作用中起作用。据报道,与COX-2酶相关的几种单核苷酸多态性(SNP)可以调节其表达。本研究的目的是检查这些SNP与巴基斯坦患者患乳腺癌的风险之间的关系。方法在本病例对照研究中,筛选了COX-2启动子区域的三个序列变体rs689465,rs689466,rs20417,以评估其与乳腺癌风险的相关性。对150例乳腺癌患者和101例健康对照基因组DNA进行了rs689456,rs689466,rs20417的基因分型,并使用Pearson卡方检验比较了病例和对照组的基因型分布。通过逻辑回归计算的奇数比分析风险关联。结果对101名健康对照者的COX-2 SNPs进行的筛选分析显示,SNPs的次要等位基因频率分布如下:rs689465(0.12),rs689466(0.15),rs20417(0.23)。进一步的分析表明,他们观察到的基因型频率与哈迪·温伯格平衡一致,并且在rs20417,rs689465和rs689466之间鉴定到强连锁不平衡。组合等位基因变体分析显示,Haplotype rs68965G- 689466A-20417C(OR 2.909; CI 95%1.3776.327; P = 0.007)与乳腺癌显着相关。结论我们的结果表明,在单基因座分析中研究的三个最常见的COX-2 SNP rs689465 rs689466,rs20417与乳腺癌风险之间没有密切关联。但是,我们的数据表明,联合COX-2 SNP单倍型在巴基斯坦患者的乳腺癌相关风险中起作用。

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