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细胞周期蛋白D1基因多态性与肝细胞癌遗传易感性的相关性
引用本文:朱忠政,丛文铭,冼志红,吴伟清,吴孟超,朱冠山. 细胞周期蛋白D1基因多态性与肝细胞癌遗传易感性的相关性[J]. 中华肿瘤防治杂志, 2007, 14(20): 1521-1523
作者姓名:朱忠政  丛文铭  冼志红  吴伟清  吴孟超  朱冠山
作者单位:1. 中国人民解放军第113医院病理科,浙江,宁波,315040;第二军医大学东方肝胆外科医院病理科,上海,200438
2. 第二军医大学东方肝胆外科医院病理科,上海,200438
3. 上海基康生物技术有限公司,上海,201203
基金项目:国家自然科学基金;上海市优秀学科带头人项目
摘    要:目的:探讨细胞周期蛋白D1(Cy-clinD1)基因A870G多态性与肝细胞癌(hepatocellular carcinoma,HCC)遗传易感性的关系。方法:采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法,检测225例HCC与428名对照的CyclinD1A870G基因型分布及差异。结果:全样本以及男性样本HCC与对照间的基因型分布差异均无统计学意义。但在女性,HCC组870G等位基因频率显著高于对照组(53.2%vs42.0%),P=0.012。与A/A纯合子相比,A/G杂合子的HCC风险增加至1.54倍(95%CI:0.79~3.01),P=0.202,而G/G纯合子的HCC风险显著增加至2.63倍(95%CI:1.20~5.78),P=0.016。结论:CyclinD1870G增加女性HCC发病风险,G/G基因型是女性患HCC的一个遗传易感因素。

关 键 词:肝肿瘤/遗传学  细胞周期蛋白D1  多态性,限制性片段长度  病例对照研究
文章编号:1673-5269(2007)20-1521-03
收稿时间:2007-07-18
修稿时间:2007-09-23

Correlation of Cyclin D1 polymorphism with genetic susceptibility to hepatocellular carcinoma
ZHU Zhong-zheng,CONG Wen-ming,XIAN Zhi-hong,WU Wei-qing,WU Meng-chao,ZHU Guan-shan. Correlation of Cyclin D1 polymorphism with genetic susceptibility to hepatocellular carcinoma[J]. Chinese Journal of Cancer Prevention and Treatment, 2007, 14(20): 1521-1523
Authors:ZHU Zhong-zheng  CONG Wen-ming  XIAN Zhi-hong  WU Wei-qing  WU Meng-chao  ZHU Guan-shan
Abstract:OBJECTIVE:To evaluate the correlation of Cyclin D1 A870G polymorphism with genetic susceptibility to hepatocellular carcinoma (HCC) in a Chinese population. METHODS: Two hundred and twenty-five HCC cases and 428 controls were studied. The Cyclin D1 genotypes were determined by a PCR-based restriction fragment length polymorphism (RFLP) method. RESULTS: Overall, no correlation between HCC and the A870G genotypes was found when comparing all HCC cases to the controls or when comparing the male cases to the male controls. However, in the females, the Cyclin D1 870G allele was more frequently observed in the HCC group (53.2% vs 42.0%, P=0.012) than the control group. As compared with A/A homozygotes, A/G heterozygotes had a 1.54-fold increased risk (95%CI: 0.79-3.01, P=0.202), whereas G/G homozygotes had a 2.63-fold (95%CI: 1.20-5.78, P=0.016) increased risk for HCC. CONCLUSION: The G allele of the Cyclin D1 A870G polymorphism is correlated with the presence of HCC and G/G homozygote is potentially one of the genetic risk factors for HCC in females.
Keywords:liver neoplasms/genetics  cyclin D1  polymorphism   restriction fragment length polymorphism  case-control study
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