Suppr超能文献

细胞周期控制基因遗传多态性与中国女性子宫内膜癌易感性的关联。

Association of genetic polymorphisms in cell-cycle control genes and susceptibility to endometrial cancer among Chinese women.

机构信息

Vanderbilt Epidemiology Center, Vanderbilt University, 2525 West End Avenue, Nashville, TN 37203-1738, USA.

出版信息

Am J Epidemiol. 2011 Jun 1;173(11):1263-71. doi: 10.1093/aje/kwr002. Epub 2011 Mar 31.

Abstract

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.

摘要

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。

相似文献

引用本文的文献

本文引用的文献

8
Low penetrance breast cancer predisposition SNPs are site specific.低外显率乳腺癌易感单核苷酸多态性具有位点特异性。
Breast Cancer Res Treat. 2009 Sep;117(1):151-9. doi: 10.1007/s10549-008-0235-7. Epub 2008 Nov 13.
10
Alteration of cell-cycle regulation in epithelial ovarian cancer.上皮性卵巢癌中细胞周期调控的改变。
Int J Gynecol Cancer. 2008 Nov-Dec;18(6):1169-82. doi: 10.1111/j.1525-1438.2008.01191.x. Epub 2008 Feb 19.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验