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长链非编码RNA H19中的标签单核苷酸多态性与中国汉族人群的胃癌易感性相关。

Tag SNPs in long non-coding RNA H19 contribute to susceptibility to gastric cancer in the Chinese Han population.

作者信息

Yang Chao, Tang Ran, Ma Xiang, Wang Younan, Luo Dakui, Xu Zekuan, Zhu Yi, Yang Li

机构信息

Department of General Surgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.

Jiangsu Province Academy of Clinical Medicine, Institute of Tumor Biology, Nanjing, China.

出版信息

Oncotarget. 2015 Jun 20;6(17):15311-20. doi: 10.18632/oncotarget.3840.

Abstract

Long non-coding RNA (lncRNA) H19 is involved in tumor development, progression, and metastasis. This case-control study assessed the association between H19 genetic variants and susceptibility to gastric cancer (GC) in a Chinese Han population. We genotyped four lncRNA H19 single nucleotide polymorphisms (SNPs) (rs217727 C > T, rs2839698 C > T, rs3741216 A > T, rs3741219 T > C) in 500 GC patients and 500 healthy controls. Carriers of variant rs217727T and rs2839698T alleles showed increased GC risk (P = 0.008 and 0.011, respectively). Compared with the common genotype, CT + TT rs217727 and CT + TT rs2839698 genotypes were associated with significantly increased GC risk (P = 0.040, adjusted odds ratio [OR] = 1.32, 95% confidence interval [CI] = 1.01-1.71; P = 0.033, adjusted OR = 1.31, 95% CI = 1.02-1.69, respectively). Further stratified analyses revealed that the association between GC risk and variant genotypes of rs217727 was more profound in younger individuals (≤59 years) and non-smokers, while the association between risk and the rare rs2839698 genotype persisted in men and rural subjects. rs2839698 CT and TT genotypes were also associated with higher serum H19 mRNA levels compared with the CC genotype. These findings suggest that lncRNA H19 SNPs may contribute to susceptibility to GC.

摘要

长链非编码RNA(lncRNA)H19参与肿瘤的发生、发展和转移。本病例对照研究评估了中国汉族人群中H19基因变异与胃癌(GC)易感性之间的关联。我们对500例GC患者和500例健康对照进行了4个lncRNA H19单核苷酸多态性(SNP)(rs217727 C>T、rs2839698 C>T、rs3741216 A>T、rs3741219 T>C)的基因分型。rs217727T和rs2839698T等位基因携带者的GC风险增加(P分别为0.008和0.011)。与常见基因型相比,rs217727的CT+TT基因型和rs2839698的CT+TT基因型与GC风险显著增加相关(P=0.040,调整优势比[OR]=1.32,95%置信区间[CI]=1.01-1.71;P=0.033,调整OR=1.31,95%CI=1.02-1.69)。进一步的分层分析显示,rs217727的GC风险与变异基因型之间的关联在较年轻个体(≤59岁)和非吸烟者中更为显著,而风险与罕见的rs2839698基因型之间的关联在男性和农村受试者中持续存在。与CC基因型相比,rs2839698的CT和TT基因型也与更高的血清H19 mRNA水平相关。这些发现表明,lncRNA H19 SNP可能与GC易感性有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f1c8/4558153/02692d23d430/oncotarget-06-15311-g001.jpg

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