SNP-SNP interactions between dNTP supply enzymes and mismatch DNA repair in breast cancer.

I Jung Feng, Tomas Radivoyevitch
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引用次数: 6

Abstract

The dNTP supply system genes RRM1, DCTD, TYMS, TK1 and DCK balance dNTP pools to avoid incorrect insertions of bases (i.e. DNA mismatches) and the DNA mismatch repair system genes MLH1 and MSH2 are involved in removing such mismatches. The objective of this study is to explore the possibility of interactions between these two systems, since greater mismatch production rates are expected to be more detrimental in cells that also have compromised mismatch removal rates. This conjecture was explored here specifically with respect to the development of breast cancer. More than 2400 breast cancer cases and controls are included in the Cancer Genetic Markers of Susceptibility (CGEMS) single nucleotide polymorphism (SNP) dataset. For each of these individuals, a total of 99 SNPs (69 dNTP supply SNPs and 30 mismatch repair SNPs) and 2070 SNP-SNP interactions between these two groups were evaluated for their effect on breast cancer using logistic regression to compute odds ratios (ORs) and corresponding 95% confidence intervals (CIs). Of these, 12 SNPs had found statistically significant associations with breast cancer individually (Four of them to decrease risk and eight of them to increase risk) and 697 of 2070 two-way interactions were significant associated with the risk of breast cancer. Thus, our study suggests that mismatches contribute to the formation of breast cancer.

乳腺癌dNTP供应酶与错配DNA修复之间的SNP-SNP相互作用。
dNTP供应系统基因RRM1、DCTD、TYMS、TK1和DCK平衡dNTP池以避免碱基错误插入(即DNA错配),DNA错配修复系统基因MLH1和MSH2参与消除这种错配。本研究的目的是探索这两个系统之间相互作用的可能性,因为在错配去除率受损的细胞中,更大的错配产生率预计会更有害。这个猜想在这里被专门探讨了关于乳腺癌的发展。超过2400例乳腺癌病例和对照组被纳入癌症易感性遗传标记(CGEMS)单核苷酸多态性(SNP)数据集。对于这些个体,使用逻辑回归计算比值比(or)和相应的95%置信区间(ci),评估了这两组之间共99个snp(69个dNTP供应snp和30个错配修复snp)和2070个SNP-SNP相互作用对乳腺癌的影响。其中,12个snp被发现与乳腺癌有统计学意义上的显著关联(其中4个降低风险,8个增加风险),2070个双向相互作用中有697个与乳腺癌风险显著相关。因此,我们的研究表明,不匹配有助于乳腺癌的形成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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