Yang Xiao, Li Pengchao, Tao Jun, Qin Chao, Cao Qiang, Gu Jinbao, Deng Xiaheng, Wang Jun, Liu Xuzhong, Wang Zijie, Wu Bian, Gu Min, Lu Qiang, Yin Changjun
Department of Urology, The First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Int J Genomics. 2014;2014:612972. doi: 10.1155/2014/612972. Epub 2014 May 7.
Nuclear factor- κ B is associated with the pathogenesis of numerous malignancies, and the functional polymorphism -94ins/del ATTG (rs28362491) in the human NFKB1 gene is associated with cancer risk. Previous studies on the association between the -94ins/del ATTG polymorphism and cancer risk reported conflicting results. To clarify this relationship, we performed a meta-analysis of 21 case-control studies involving 6127 cases and 9238 controls. We used pooled odds ratios (ORs) with their 95% confidence intervals (95% CIs) to assess the association. We found that the NFKB1 promoter -94ins/del ATTG polymorphism was significantly associated with cancer risk in four genetic models (ins/ins versus del/del, OR = 1.47, 95% CI = 1.11-1.93; dominant model, OR = 1.26, 95% CI = 1.03-1.53; recessive model, OR = 1.26, 95% CI = 1.05-1.51; ins allele versus del allele, OR = 1.19, 95% CI = 1.05-1.35). Stratified analyses revealed a significant association between the polymorphism and ovarian, oral, and prostate cancers. Similar results were determined in an Asian population and not in a Caucasian population. Thus, our results suggested that the polymorphism can contribute to cancer risk. Moreover, the polymorphism can exert race- and cancer-specific effects on cancer risk. Further large-scale and functional studies are necessary to elucidate this possible effect.
核因子-κB与多种恶性肿瘤的发病机制相关,人类NFKB1基因中的功能性多态性-94ins/del ATTG(rs28362491)与癌症风险相关。先前关于-94ins/del ATTG多态性与癌症风险之间关联的研究报告了相互矛盾的结果。为了阐明这种关系,我们对21项病例对照研究进行了荟萃分析,涉及6127例病例和9238例对照。我们使用合并比值比(OR)及其95%置信区间(95%CI)来评估这种关联。我们发现,在四种遗传模型中,NFKB1启动子-94ins/del ATTG多态性与癌症风险显著相关(ins/ins与del/del相比,OR = 1.47,95%CI = 1.11-1.93;显性模型,OR = 1.26,95%CI = 1.03-1.53;隐性模型,OR = 1.26,95%CI = 1.05-1.51;ins等位基因与del等位基因相比,OR = 1.19,95%CI = 1.05-1.35)。分层分析显示该多态性与卵巢癌、口腔癌和前列腺癌之间存在显著关联。在亚洲人群中得出了类似结果,而在白种人群中未得出类似结果。因此,我们的结果表明该多态性可能导致癌症风险。此外,该多态性可能对癌症风险产生种族和癌症特异性影响。需要进一步开展大规模和功能性研究来阐明这种可能的影响。