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hoGG1 基因 5'-UTR 区两个功能变异与中国人群乳腺癌发病风险相关。

Two functional variations in 5'-UTR of hoGG1 gene associated with the risk of breast cancer in Chinese.

机构信息

Department of Medical Genetics, Nanjing University School of Medicine, Nanjing 210093, China.

出版信息

Breast Cancer Res Treat. 2011 Jun;127(3):795-803. doi: 10.1007/s10549-010-1284-2. Epub 2010 Dec 14.

DOI:10.1007/s10549-010-1284-2
PMID:21153698
Abstract

8-Hydroxy-2'-deoxyguanine (8-OHdG) is produced by the oxidative stress-induced damage in DNA, which could pair with adenine (A) during DNA replication, leading to G-T transversion mutations. Glycosylase hOGG1 can recognize and excise oxidized guanines from duplex DNA. This work aims to investigate the relationship between the functional variations in 5-untranslated region (5'-UTR) of hOGG1 gene and the risk of breast cancer. Genotypes were analyzed in 518 sporadic breast cancer patients and 777 health controls. Odds ratios (ORs) and 95% confidence intervals (CIs) were estimated by logistic regression. Risk-stratified subgroup analysis was performed to reveal the associations between the detected variations and the risk of characteristic breast cancer. In addition, immunohistochemistry was carried out to assess the functional effect of these variations on hOGG1gene expression. Five variations in 5'-UTR of hOGG1 gene are found in this study. Three of them, c.-18G>T, c.-23A>G, and c.-53G>C, are known single nucleotide polymorphisms, the other two, c.-45G>A and c.-63G>C, are rare variations. The frequency of c.-18G/T and c.-53G/C was significantly higher in breast cancer patients than those in healthy controls (P = 0.03, OR 2.01, 95% CI 1.04-3.90; and P = 0.01, OR 2.43, 95% CI 1.17-5.04, respectively). Both variations were especially prevalent in premenopausal status, and in the triple (estrogen receptor, progesterone receptor, and human epidermal growth factor Receptor 2) negative subgroups, respectively. Moreover, the variation of c.-18G>T could cause a reduced expression of hOGG1 gene.

摘要

8-羟基-2'-脱氧鸟嘌呤(8-OHdG)是由 DNA 氧化应激损伤产生的,它可以在 DNA 复制时与腺嘌呤(A)配对,导致 G-T 颠换突变。糖苷酶 hOGG1 可以识别并从双链 DNA 中切除氧化的鸟嘌呤。本研究旨在探讨 hOGG1 基因 5'非翻译区(5'-UTR)的功能变异与乳腺癌风险之间的关系。在 518 例散发性乳腺癌患者和 777 例健康对照中分析了基因型。采用 logistic 回归估计比值比(OR)和 95%置信区间(CI)。进行风险分层亚组分析,以揭示检测到的变异与特征性乳腺癌风险之间的关联。此外,还进行了免疫组织化学分析,以评估这些变异对 hOGG1 基因表达的功能影响。在本研究中发现 hOGG1 基因 5'-UTR 中有 5 个变异。其中 3 个,c.-18G>T、c.-23A>G 和 c.-53G>C,是已知的单核苷酸多态性,另外 2 个,c.-45G>A 和 c.-63G>C,是罕见的变异。c.-18G/T 和 c.-53G/C 的频率在乳腺癌患者中明显高于健康对照组(P=0.03,OR 2.01,95%CI 1.04-3.90;P=0.01,OR 2.43,95%CI 1.17-5.04)。这两种变异在绝经前状态和三阴性(雌激素受体、孕激素受体和人表皮生长因子受体 2)阴性亚组中尤为常见。此外,c.-18G>T 的变异可导致 hOGG1 基因表达减少。

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