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核因子-κB1与中国人群的胃癌相关。

Nuclear factor-kappa B1 is associated with gastric cancer in a Chinese population.

作者信息

Hua Tang, Qinsheng Wen, Xuxia Wang, Shuguang Zhao, Ming Qin, Zhenxiong Liu, Jingjie Wang

机构信息

From the Department of Gastroenterology, Tangdu Hospital, Fourth Military Medical University of China, Xi'an, Shaanxi, China.

出版信息

Medicine (Baltimore). 2014 Dec;93(28):e279. doi: 10.1097/MD.0000000000000279.

Abstract

Activated nuclear factor-κB (NF-κB) is associated with the pathogenesis of numerous cancers, such as gastric cancer (GC). Genetic polymorphisms in the genomic region containing nuclear factor-κB1 (NFKB1) have a plausible role in modulating the risk of GC. To identify markers contributing to the genetic susceptibility to GC, we analyzed 15 single nucleotide polymorphisms (SNPs, rs28362491, rs3774932, rs1598856, rs230531, rs230530, rs230528, rs230521, rs230498, rs230539, rs1005819, rs3774956, rs4648055, rs3774964, rs4648068, and rs3774968) in the genomic region containing NFKB1. The participants included 401 patients with GC and 433 healthy controls. The allelic or genotypic frequencies of the rs28362491 (located in the promoter region of NFKB1), rs230521 (NFKB1 intron 4), and rs4648068 (NFKB1 intron 12) polymorphisms in the patients with GC were significantly different from those in the healthy controls. Strong linkage disequilibrium was observed in 4 blocks (D'>0.9). Significantly more A-T haplotypes (block 1, P=0.0005), A-C haplotypes (block 2, P=0.0001) and G-A-A haplotypes (block 4, P=0.016) were found in the patients with GC. Significantly more A-C haplotypes (block 1, P=0.005) and A-G haplotypes (block 2, P=0.0004) were found in the healthy controls. These findings suggest a role for NFKB1 polymorphism in GC among a Han Chinese population and may be informative for future genetic studies on gastric cancer.

摘要

活化的核因子-κB(NF-κB)与多种癌症的发病机制相关,如胃癌(GC)。包含核因子-κB1(NFKB1)的基因组区域中的基因多态性在调节GC风险方面可能发挥作用。为了确定导致GC遗传易感性的标志物,我们分析了包含NFKB1的基因组区域中的15个单核苷酸多态性(SNP,rs28362491、rs3774932、rs1598856、rs230531、rs230530、rs230528、rs230521、rs230498、rs230539、rs1005819、rs3774956、rs4648055、rs3774964、rs4648068和rs3774968)。参与者包括401例GC患者和433例健康对照。GC患者中rs28362491(位于NFKB1启动子区域)、rs230521(NFKB1内含子4)和rs4648068(NFKB1内含子12)多态性的等位基因或基因型频率与健康对照有显著差异。在4个区域观察到强连锁不平衡(D'>0.9)。在GC患者中发现显著更多的A-T单倍型(区域1,P=0.0005)、A-C单倍型(区域2,P=0.0001)和G-A-A单倍型(区域4,P=0.016)。在健康对照中发现显著更多的A-C单倍型(区域1,P=0.005)和A-G单倍型(区域2,P=0.0004)。这些发现提示NFKB1多态性在汉族人群的GC中发挥作用,可能为未来胃癌的遗传研究提供信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f49/4603084/9d8779d925d0/medi-93-e279-g001.jpg

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