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HOGG1 Ser326Cys 多态性与中国人群肾细胞癌风险。

hOGG1 Ser326Cys polymorphism and renal cell carcinoma risk in a Chinese population.

机构信息

Department of Urology, The Affiliated Jiangyin Hospital of Southeast University Medical College, Wuxi, China.

出版信息

DNA Cell Biol. 2011 May;30(5):317-21. doi: 10.1089/dna.2010.1135. Epub 2010 Dec 17.

DOI:10.1089/dna.2010.1135
PMID:21166493
Abstract

Oxidative DNA damage caused by reactive oxygen species plays an important role in cancer development. Human 8-oxoguanine DNA glycosylase (hOGG1) is involved in base excision repair of 8-oxoguanine from damaged DNA. We hypothesized that variants in the hOGG1 gene are associated with risk of renal cell carcinoma (RCC). In a hospital-based case-control study of 572 RCC patients and 575 cancer-free controls frequency matched by age and sex, we genotyped the functional polymorphism Ser326Cys (rs1052133) and assessed its associations with risk of RCC in a Chinese population. We found that individuals with the Cys allele were associated with an increased risk of RCC (odds ratio [OR] = 1.40, 95% confidence interval [CI] = 1.02-1.90), compared with those with the Ser/Ser genotype, particularly among subgroups of body mass index >24 kg/m(2) (OR = 1.75, 95% CI = 1.12-2.73) and non-smokers (OR = 1.60, 95% CI = 1.07-2.38). Further, the polymorphism was associated with risk of developing localized stage and well-differentiated RCC. Our results suggested that the polymorphism is involved in the etiology of RCC and thus may be a marker for genetic susceptibility to RCC.

摘要

活性氧自由基引起的氧化 DNA 损伤在癌症发展中起着重要作用。人类 8-氧鸟嘌呤 DNA 糖基化酶(hOGG1)参与受损 DNA 中 8-氧鸟嘌呤的碱基切除修复。我们假设 hOGG1 基因中的变异与肾细胞癌(RCC)的风险相关。在一项基于医院的 572 例 RCC 患者和 575 例癌症对照病例对照研究中,我们对功能性多态性 Ser326Cys(rs1052133)进行了基因分型,并评估了其在中国人群中与 RCC 风险的相关性。我们发现,与 Ser/Ser 基因型相比,携带 Cys 等位基因的个体患 RCC 的风险增加(比值比 [OR] = 1.40,95%置信区间 [CI] = 1.02-1.90),尤其是在体重指数(BMI)>24 kg/m(2)(OR = 1.75,95% CI = 1.12-2.73)和非吸烟者(OR = 1.60,95% CI = 1.07-2.38)亚组中。此外,该多态性与局限性和分化良好的 RCC 发病风险相关。我们的结果表明,该多态性参与了 RCC 的病因学,因此可能是 RCC 遗传易感性的标志物。

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