Li Yuying, Du Zhonghua, Wang Xu, Wang Guanjun, Li Wei
Cancer Center, First Hospital of Jilin University , Changchun, China .
Genet Test Mol Biomarkers. 2016 Oct;20(10):587-596. doi: 10.1089/gtmb.2015.0169. Epub 2016 Aug 15.
A number of studies show that the pleiotropic cytokine interleukin-6 (IL-6) plays an important role in the pathogenesis of multiple myeloma (MM). However, whether MM risk is associated with IL-6 genetic variability remains uncertain.
The aim of our study was to evaluate the association between two different IL-6 polymorphisms (located in the IL-6 promoter and receptor, respectively) and the risk of developing MM using a meta-analytic approach.
A systematic search for studies on the association of IL-6/IL-6R single-nucleotide polymorphisms with susceptibility to MM was conducted in PubMed, Cochrane Library, Embase, CNKI (Chinese) and Wanfang (Chinese) Digital Dissertations Databases from inception through November 2014. A meta-analysis was performed and results were presented as odds ratios (ORs) with 95% confidence intervals (CIs).
A total of eight case-control studies on the IL-6 promoter polymorphism and three studies on the IL-6 receptor (IL-6R) polymorphism were included. No significant association was found between the IL-6 promoter rs1800795 (G>C) polymorphism and MM susceptibility. A significantly increased risk of MM was observed with the IL-6R rs8192284 (A>C) polymorphism. In subgroup analyses, grouped by ethnicity, region, quality of studies, and Hardy-Weinberg equilibrium of control group, similar results were found.
Unlike the IL-6 promoter rs1800795 (G>C) polymorphism, the IL-6R rs8192284 (A>C) polymorphism may be associated with MM risk. However, large-scale studies are needed to validate our findings since they are based on a relatively small number of studies.
多项研究表明,多效细胞因子白细胞介素 - 6(IL - 6)在多发性骨髓瘤(MM)的发病机制中起重要作用。然而,MM风险是否与IL - 6基因变异性相关仍不确定。
我们研究的目的是采用荟萃分析方法评估两种不同的IL - 6多态性(分别位于IL - 6启动子和受体中)与发生MM风险之间的关联。
在PubMed、Cochrane图书馆、Embase、中国知网(中文)和万方(中文)学位论文数据库中,对从数据库建立至2014年11月期间关于IL - 6/IL - 6R单核苷酸多态性与MM易感性关联的研究进行系统检索。进行荟萃分析,并将结果表示为比值比(OR)及95%置信区间(CI)。
共纳入8项关于IL - 6启动子多态性的病例对照研究和3项关于IL - 6受体(IL - 6R)多态性的研究。未发现IL - 6启动子rs1800795(G>C)多态性与MM易感性之间存在显著关联。观察到IL - 6R rs8192284(A>C)多态性使MM风险显著增加。在按种族、地区、研究质量和对照组的哈迪 - 温伯格平衡分组的亚组分析中,发现了类似结果。
与IL - 6启动子rs1800795(G>C)多态性不同,IL - 6R rs8192284(A>C)多态性可能与MM风险相关。然而,由于我们的发现基于相对较少的研究,因此需要大规模研究来验证我们的结果。