Collaborative Innovation Center For Cancer Personalized Medicine, Nanjing Medical University; Department of Oral and Maxillofacial Surgery, Affiliated Hospital of Stomatology, Nanjing Medical University, Nanjing, China.
Department of Medicine, Duke University School of Medicine, Durham, NC, USA.
Sci Rep. 2016 Oct 7;6:34234. doi: 10.1038/srep34234.
Lung cancer etiology is multifactorial, and growing evidence has indicated that long non-coding RNAs (lncRNAs) are important players in lung carcinogenesis. We performed a large-scale meta-analysis of 690,564 SNPs in 15,531 autosomal lncRNAs by using datasets from six previously published genome-wide association studies (GWASs) from the Transdisciplinary Research in Cancer of the Lung (TRICL) consortium in populations of European ancestry. Previously unreported significant SNPs (P value < 1 × 10) were further validated in two additional independent lung cancer GWAS datasets from Harvard University and deCODE. In the final meta-analysis of all eight GWAS datasets with 17,153 cases and 239,337 controls, a novel risk SNP rs114020893 in the lncRNA NEXN-AS1 region at 1p31.1 remained statistically significant (odds ratio = 1.17; 95% confidence interval = 1.11-1.24; P = 8.31 × 10). In further in silico analysis, rs114020893 was predicted to change the secondary structure of the lncRNA. Our finding indicates that SNP rs114020893 of NEXN-AS1 at 1p31.1 may contribute to lung cancer susceptibility.
肺癌的病因是多因素的,越来越多的证据表明,长非编码 RNA(lncRNAs)是肺癌发生的重要参与者。我们通过使用来自欧洲血统人群的六个先前发表的全基因组关联研究(GWAS)数据集,对 15531 个常染色体 lncRNA 中的 690564 个 SNP 进行了大规模的荟萃分析。在另外两个来自哈佛大学和 deCODE 的独立肺癌 GWAS 数据集进一步验证了先前未报道的显著 SNP(P 值<1×10)。在包含 17153 例病例和 239337 例对照的所有八个 GWAS 数据集的最终荟萃分析中,在 1p31.1 上的 lncRNA NEXN-AS1 区域中的新型风险 SNP rs114020893 仍然具有统计学意义(优势比=1.17;95%置信区间=1.11-1.24;P=8.31×10)。在进一步的计算分析中,rs114020893 被预测会改变 lncRNA 的二级结构。我们的研究结果表明,1p31.1 上的 NEXN-AS1 的 SNP rs114020893 可能导致肺癌易感性。