Vanderbilt Epidemiology Center, Vanderbilt University, 2525 West End Avenue, Nashville, TN 37203-1738, USA.
Am J Epidemiol. 2011 Jun 1;173(11):1263-71. doi: 10.1093/aje/kwr002. Epub 2011 Mar 31.
Although genetic variations in cell-cycle control genes have been previously linked to cancer risk, no study has specifically evaluated the role of these gene variants in endometrial carcinogenesis. Using data from the Shanghai Endometrial Cancer Study, a population-based case-control study with 1,199 cases and 1,212 age-matched controls (1997-2003), the authors carried out a systematic evaluation of the association of cell-cycle control genes with endometrial cancer risk. Sixty-five tagging or potentially functional single nucleotide polymorphisms in the CCNB1, CCND1, CCNE1, CDK2, CDK4, CDK6, CDKN1A, CDKN1B, and CDKN2A genes were genotyped and evaluated. Three single nucleotide polymorphisms in the CDKN1B gene (rs11055027, rs3759216, and rs34330) were related to endometrial cancer risk, although only the association with rs34330 remained statistically significant after adjustment for multiple comparisons. The odds ratios for rs34330 were 1.33 (95% confidence interval (CI): 1.06, 1.66) and 1.51 (95% CI: 1.16, 1.94) for the CT and TT genotypes, respectively, compared with the CC genotype. In vitro luciferase reporter assays showed that the minor allele (A) in rs3759216, which was associated with decreased endometrial cancer risk (odds ratio = 0.73, 95% CI: 0.56, 0.94) without adjustment for multiple comparisons, significantly increased promoter activity. These findings suggest that polymorphisms of the CDKN1B gene may play a role in endometrial carcinogenesis.
虽然细胞周期控制基因的遗传变异先前与癌症风险有关,但尚无研究专门评估这些基因变异在子宫内膜癌发生中的作用。本研究利用上海子宫内膜癌研究的数据(1997-2003 年开展的一项基于人群的病例对照研究,共纳入 1199 例病例和 1212 名年龄匹配的对照),对细胞周期控制基因与子宫内膜癌风险的关联进行了系统评价。对 CCNB1、CCND1、CCNE1、CDK2、CDK4、CDK6、CDKN1A、CDKN1B 和 CDKN2A 基因中的 65 个标记或潜在功能单核苷酸多态性进行了基因分型和评估。CDKN1B 基因中的 3 个单核苷酸多态性(rs11055027、rs3759216 和 rs34330)与子宫内膜癌风险相关,然而,在进行多次比较调整后,仅 rs34330 与子宫内膜癌风险的关联仍具有统计学意义。与 CC 基因型相比,rs34330 的 CT 和 TT 基因型的比值比(OR)分别为 1.33(95%置信区间[CI]:1.06,1.66)和 1.51(95% CI:1.16,1.94)。体外荧光素酶报告基因检测显示,rs3759216 的次要等位基因(A)与子宫内膜癌风险降低相关(OR=0.73,95% CI:0.56,0.94),未经多次比较调整。这些发现提示 CDKN1B 基因的多态性可能在子宫内膜癌发生中发挥作用。