Department of Epidemiology and Biostatistics, School of Public Health, Nantong University, Nantong, 226019, China.
Department of Epidemiology and Biostatistics, Collaborative Innovation Center for Cancer Personalized Medicine, School of Public Health, Nanjing Medical University, Nanjing, 211166, China.
Gastric Cancer. 2017 Nov;20(6):940-947. doi: 10.1007/s10120-017-0717-6. Epub 2017 Apr 13.
The cysteinyl transfer RNA synthetase gene (CARS) is located on chromosome band 11p15.5, which is an important tumor-suppressor gene region. Mutations in CARS have been identified in many kinds of cancers; however, evidence for a relationship between genetic variants in CARS and gastric cancer at the population level is still lacking. Thus, we explored the association of variants in CARS with gastric cancer using a two-stage case-control strategy in Chinese.
We undertook a two-stage case-control study to investigate the association between polymorphisms in CARS and risk of gastric cancer with use of an Illumina Infinium BeadChip and an ABI 7900 system.
Four single nucleotide polymorphisms (SNPs) were significantly associated with gastric cancer risk in both the discovery stage and the validation stage after adjustment for age and sex. In addition, the combined results of the two stages showed these SNPs were related to gastric cancer risk (P ≤ 0.001 for rs384,490, rs729662, rs2071101, and rs7394702). In silico analyses revealed that rs384490 and rs7394702 could affect transcription factor response elements or DNA methylation of CARS, and rs729662 was associated with the prognosis of gastric cancer. Additionally, expression quantitative trait loci analysis showed rs384490 and rs729662 might alter expression of CARS-related genes.
The potential functional SNPs in CARS might influence the biological functions of CARS or CARS-related genes and ultimately modify the occurrence and development of gastric cancer in Chinese. Further large-scale population-based studies or biological functional assays are warranted to validate our findings.
半胱氨酰 tRNA 合成酶基因(CARS)位于染色体 11p15.5 带,是一个重要的肿瘤抑制基因区域。CARS 中的突变已在许多癌症中被发现;然而,人群中 CARS 基因遗传变异与胃癌之间的关系证据仍然缺乏。因此,我们使用中国的两阶段病例对照策略探讨了 CARS 变异与胃癌之间的关联。
我们进行了两阶段病例对照研究,使用 Illumina Infinium BeadChip 和 ABI 7900 系统调查 CARS 多态性与胃癌风险之间的关联。
在调整年龄和性别后,在发现阶段和验证阶段,有四个单核苷酸多态性(SNP)与胃癌风险显著相关。此外,两个阶段的合并结果表明这些 SNP 与胃癌风险相关(rs384,490、rs729662、rs2071101 和 rs7394702 的 P 均 ≤ 0.001)。 基于计算机的分析表明,rs384490 和 rs7394702 可能影响 CARS 的转录因子反应元件或 DNA 甲基化,rs729662 与胃癌的预后相关。此外,表达数量性状基因座分析表明 rs384490 和 rs729662 可能改变 CARS 相关基因的表达。
CARS 中的潜在功能 SNP 可能影响 CARS 或 CARS 相关基因的生物学功能,最终改变中国人胃癌的发生和发展。需要进一步进行大规模的基于人群的研究或生物学功能检测来验证我们的发现。