Gao Yue, Liu Yan, Liu Ge-Li, Ran Long-Ke, Zeng Fan, Wu Jia-Yan, Song Fang-Zhou
Molecular Medicine and Cancer Research Center, Chongqing Medical University, Chongqing, China E-mail :
Asian Pac J Cancer Prev. 2014;15(6):2517-22. doi: 10.7314/apjcp.2014.15.6.2517.
Several recent studies have explored associations between pre-mir-218 polymorphism (rs11134527) and cancer risk. However, published data are still inconclusive. To obtain a more precise estimation of the relationship in the Chinese population, we carried out a meta-analysis for the first time.
Through retrieval from the PubMed, Medline, Embase, Web of Science databases, China National Knowledge Infrastructure and the Chinese BioMedical Literature Database, a total of four studies were analyzed with 3,561 cases and 3,628 controls for SNP pre-mir-218 rs11134527. We calculated odds ratios (ORs) and 95% confidence intervals (95%CIs) to explore the strength of associations.
The results showed that the rs11134527 polymorphism was associated with decreased cancer risk in GG versus AA and GG versus AA+AG models tested ( GG vs AA: OR=0.82, 95%CI: 0.71-0.94; GG vs AA+AG: OR=0.84, 95%CI: 0.74-0.96), and significantly decreased cervical cancer risk was observed in GG versus AA and GG versus AA+AG models (GG vs AA: OR=0.79, 95%CI: 0.66-0.94; GG vs AA+AG: OR=0.80, 95%CI: 0.68-0.94). However, no significant association between the rs11134527 polymorphism and hepatocellular carcinoma risk was observed in all comparison models tested (AG vs AA: OR=0.94, 95%CI: 0.79-1.11; GG vs AA: OR=0.88, 95%CI: 0.70-1.10; GG+AG vs AA: OR=0.92, 95%CI: 0.79-1.08; GG vs AA+AG: OR=0.91, 95%CI: 0.75-1.11).
The findings suggest that pre-miR-218 rs11134527 polymorphism may have some relation to cancer development in Chinese. However, well-designed studies with larger sample size and more detailed data are needed to confirm these conclusions.
近期多项研究探讨了前体微小RNA-218多态性(rs11134527)与癌症风险之间的关联。然而,已发表的数据仍无定论。为了更精确地评估中国人群中的这种关系,我们首次进行了一项荟萃分析。
通过检索PubMed、Medline、Embase、Web of Science数据库、中国知网和中国生物医学文献数据库,共分析了4项研究,其中3561例病例和3628例对照涉及单核苷酸多态性前体微小RNA-218 rs11134527。我们计算了比值比(OR)和95%置信区间(95%CI)以探究关联强度。
结果显示,在测试的GG与AA以及GG与AA + AG模型中,rs11134527多态性与癌症风险降低相关(GG vs AA:OR = 0.82,95%CI:0.71 - 0.94;GG vs AA + AG:OR = 0.84,95%CI:0.74 - 0.96),并且在GG与AA以及GG与AA + AG模型中观察到宫颈癌风险显著降低(GG vs AA:OR = 0.79,95%CI:0.66 - 0.94;GG vs AA + AG:OR = 0.80,95%CI:0.68 - 0.94)。然而,在所有测试的比较模型中,均未观察到rs11134527多态性与肝细胞癌风险之间存在显著关联(AG vs AA:OR = 0.94,95%CI:0.79 - 1.11;GG vs AA:OR = 0.88,95%CI:0.70 - 1.10;GG + AG vs AA:OR = 0.92,95%CI:0.79 - 1.08;GG vs AA + AG:OR = 0.91,95%CI:0.75 - 1.11)。
研究结果表明,前体微小RNA-218 rs11134527多态性可能与中国人的癌症发生有一定关系。然而,需要设计更完善、样本量更大且数据更详细的研究来证实这些结论。