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生活方式因素与 EPIC-Norfolk 研究中结直肠癌患者 p53 基因突变模式的关系。

Lifestyle factors and p53 mutation patterns in colorectal cancer patients in the EPIC-Norfolk study.

机构信息

Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.

出版信息

Mutagenesis. 2010 Jul;25(4):351-8. doi: 10.1093/mutage/geq012. Epub 2010 Mar 12.

Abstract

The tumour suppressor p53 is one of the most commonly altered genes in colorectal cancer (CRC) development. Genetic alterations in p53 may therefore be associated with postulated lifestyle risk factors for CRC, such as red meat consumption. In the European Prospective Investigation into Cancer and Nutrition-Norfolk study, we examined whether detailed estimates of dietary and lifestyle factors measured at baseline related to later development of p53 mutations in CRCs. After 10-year follow-up, there were 185 incident CRCs of which 34% had somatic p53 mutations (p53+). We observed significantly higher mean intakes of alcohol, total meat and red meat, in the group with p53 mutations and advanced Dukes' stage disease (daily alcohol intake was 7 and 12 g for p53- and p53+ cases, respectively, P = 0.04; daily total meat intake was 69 and 100 g for p53- and p53+ cases, respectively, P = 0.03 and daily red meat intake was 39 and 75 g for p53- and p53+ cases, respectively, P = 0.01). Each 50 g/day increment in total meat intake was associated with having p53 mutations in cases with advanced Dukes' stages [odds ratio (OR): 3.43, 95% confidence interval (CI): 1.47-7.96]. Similarly, each 50 g/day increment in red meat intake was also significantly associated with having consistent p53 mutations in cases with advanced Dukes' stages (OR: 2.42, 95% CI: 1.18-4.96). These effects of total meat or red meat intake and advanced Dukes' stages were independent of age, sex, body mass index, smoking and alcohol intake. Furthermore, P values for interaction between daily total meat or red meat intake and Dukes' stages were statistically significant in multivariable models (Pinteraction < 0.001). Our results suggest that p53 mutations accelerate progression of CRC to advanced Dukes' stage in association with higher meat especially red meat intakes.

摘要

抑癌基因 p53 是结直肠癌 (CRC) 发展过程中最常发生改变的基因之一。因此,p53 的遗传改变可能与 CRC 的假定生活方式危险因素有关,例如食用红肉。在欧洲癌症前瞻性调查与营养-诺福克研究中,我们研究了基线时测量的饮食和生活方式因素的详细估计值是否与 CRC 中 p53 突变的后期发展有关。经过 10 年的随访,有 185 例 CRC 事件,其中 34%存在体细胞 p53 突变 (p53+)。我们观察到,p53 突变组和 Dukes 分期较晚的组的酒精、总肉和红肉的平均摄入量显著较高(p53-组和 p53+组的每日酒精摄入量分别为 7 和 12 克,P=0.04;p53-组和 p53+组的每日总肉摄入量分别为 69 和 100 克,P=0.03;p53-组和 p53+组的每日红肉摄入量分别为 39 和 75 克,P=0.01)。在 Dukes 分期较晚的病例中,总肉摄入量每增加 50 克/天,p53 突变的可能性就会增加[比值比(OR):3.43,95%置信区间(CI):1.47-7.96]。同样,在 Dukes 分期较晚的病例中,红肉摄入量每增加 50 克/天,也与持续的 p53 突变显著相关(OR:2.42,95%CI:1.18-4.96)。总肉或红肉摄入量和 Dukes 分期的这些影响独立于年龄、性别、体重指数、吸烟和饮酒。此外,在多变量模型中,总肉或红肉摄入量与 Dukes 分期之间的交互作用 P 值具有统计学意义(Pinteraction <0.001)。我们的结果表明,p53 突变与较高的肉类摄入量(尤其是红肉)相关,可加速 CRC 向 Dukes 分期晚期进展。

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