Wen Li, Hu Yuan-Yuan, Yang Gong-Li, Liu DE-Xi
Department of Dermatology, Taihe Hospital, Hubei University of Medicine, Shiyan 442000, P.R. China.
Department of Stomatology and Evidence-Based Medicine Center, Taihe Hospital, Hubei University of Medicine, Shiyan 442000, P.R. China.
Biomed Rep. 2014 Jul;2(4):549-554. doi: 10.3892/br.2014.286. Epub 2014 May 21.
The common functional cyclin D1 (CCND1) G870A polymorphism may influence the risk of esophageal cancer. However, the conclusions of previous studies have been inconsistent for the association between the CCND1 G870A polymorphism and esophageal cancer risk. A meta-analysis of 11 published case-control studies was performed, including 2,111 patients with esophageal cancer and 3,232 controls, to investigate the association between the CCND1 G870A polymorphism and esophageal cancer risk. The odds ratio (OR) with a 95% confidence interval (CI) was applied to assess the association between the CCND1 G870A polymorphism and esophageal cancer risk. A significant association between the CCND1 G870A polymorphism and esophageal cancer risk was observed for the allele contrast (A vs. G: OR, 1.23; 95% CI, 1.02-1.48; P=0.029), codominant (AA vs. GG: OR, 1.58; 95% CI; 1.06-2.35; P=0.024) and recessive models (AA vs. GG + GA: OR, 1.33, 95% CI, 1.03-1.73; P=0.030). However, in the stratified analysis by ethnicity, study design and pathology, there was no significant association detected in these genetic models. In conclusion, results of the meta-analysis suggested that the CCND1 G870A polymorphism is a potential risk factor in the development of esophageal cancer.
常见的功能性细胞周期蛋白D1(CCND1)G870A多态性可能会影响食管癌风险。然而,先前研究关于CCND1 G870A多态性与食管癌风险之间的关联所得出的结论并不一致。我们进行了一项对11项已发表的病例对照研究的荟萃分析,其中包括2111例食管癌患者和3232例对照,以探究CCND1 G870A多态性与食管癌风险之间的关联。采用比值比(OR)及95%置信区间(CI)来评估CCND1 G870A多态性与食管癌风险之间的关联。在等位基因对比(A对G:OR,1.23;95%CI,1.02 - 1.48;P = 0.029)、共显性模型(AA对GG:OR,1.58;95%CI,1.06 - 2.35;P = 0.024)和隐性模型(AA对GG + GA:OR,1.33,95%CI,1.03 - 1.73;P = 0.030)中,均观察到CCND1 G870A多态性与食管癌风险之间存在显著关联。然而,在按种族、研究设计和病理进行的分层分析中,在这些遗传模型中未检测到显著关联。总之,荟萃分析结果表明,CCND1 G870A多态性是食管癌发生的一个潜在风险因素。