Division of Molecular Medicine, Department of Laboratory Medicine, West China Hospital, Sichuan University, Chengdu, People's Republic of China.
DNA Cell Biol. 2012 Apr;31(4):524-30. doi: 10.1089/dna.2011.1340. Epub 2011 Aug 23.
MicroRNAs (miRNAs) play an important role in the growth and development of human beings. Single nucleotide polymorphisms (SNPs) within miRNA could change their production or affinity with target genes, thus leading to malignant diseases. This case-control study conducted in Western China aimed to explore the relationship between polymorphisms in miR-146a (rs2910164 G>C) and miR-499 (rs3746444 T>C) and primary liver cancers in the Chinese population. 186 primary liver cancer cases and 483 healthy controls were genotyped using polymerase chain reaction-restriction fragment length polymorphism. No significant differences were observed between distributions of the two SNPs and susceptibility of primary liver cancer or diverse clinicopathologic features. However, we found that patients with genotype CG of the SNP in miR-146a tended to have earlier onset and better liver function than patients with genotype CC (average age: 49.9 vs. 54.9, p=0.038; average Child-Pugh grade: 5.55 vs. 6.15, p=0.021), and further analysis showed that patients who had at least one G allele were diagnosed at an earlier age (average age: 49.6 vs. 54.9, p=0.022) and had better liver function (average Child-Pugh grade:5.60 vs. 6.15, p=0.026). Our data suggested lack of association between the two SNPs and primary liver cancer risk, though, interestingly, the miR-146a SNP may influence the age of onset and Child-Pugh grade.
微小 RNA(miRNA)在人类的生长和发育中起着重要作用。miRNA 中的单核苷酸多态性(SNP)可能会改变它们与靶基因的产生或亲和力,从而导致恶性疾病。本病例对照研究在中国西部进行,旨在探讨 miR-146a(rs2910164 G>C)和 miR-499(rs3746444 T>C)多态性与中国人群原发性肝癌之间的关系。使用聚合酶链反应-限制性片段长度多态性对 186 例原发性肝癌病例和 483 例健康对照进行了基因分型。两个 SNP 的分布与原发性肝癌的易感性或不同的临床病理特征之间没有观察到显著差异。然而,我们发现 miR-146a 中 SNP 的 CG 基因型患者的发病年龄较早,肝功能较好,与 CC 基因型患者相比(平均年龄:49.9 岁 vs. 54.9 岁,p=0.038;平均 Child-Pugh 分级:5.55 岁 vs. 6.15 岁,p=0.021),进一步分析显示至少携带一个 G 等位基因的患者发病年龄更早(平均年龄:49.6 岁 vs. 54.9 岁,p=0.022),肝功能更好(平均 Child-Pugh 分级:5.60 岁 vs. 6.15 岁,p=0.026)。我们的数据表明,这两个 SNP 与原发性肝癌风险之间没有关联,但有趣的是,miR-146a SNP 可能会影响发病年龄和 Child-Pugh 分级。