Qi Lei, Sun Kewen, Zhuang Yun, Yang Jing, Chen Jianping
Department of Gastroenterology, the Third Affiliated Hospital of Soochow University, Changzhou, China.
J BUON. 2017 Nov-Dec;22(6):1488-1493.
Excessive activation of PI3K/AKT/mTOR signaling pathway is one of the most common changes in human cancers, and single nucleotide polymorphisms (SNPs) existing in its functional region can affect the occurrence process of a variety of cancers. This study aimed to screen out the SNPs associated with susceptibility to gastric cancer in the PI3K/AKT/mT0R signaling pathway.
In this case-control study, the tagging SNPs in the promoter region5'-UTR, exon region or 3'-UTR of PIK3CA, PIK3CB, PIK3R1, PIK3R2, PIK3R3, AKT1, AKT2, AKT3 and mTOR genes were screened out. The relationship between the genetic variation of PI3K/AKT/mT0R signaling pathway genes and the susceptibility to gastric cancer in Chinese Han population was investigated by this casecontrol study.
The results showed that the polymorphisms of the two loci, PIK3R3 rs7536272 (Additive model: OR=1.16, 95% CI=1.01-1.35) and mTOR rs2295080 (GG vs TT: OR=0.75, 95% CI=0.60-0.94; Additive model: OR=0.78, 95% CI=0.66- 0.93), were associated with the risk of gastric cancer in the studied population and there was a combined effect between the two loci (ptrend=0.005).
In conclusion, the polymorphisms of the two loci, PIK3R3 rs7536272 and mTOR rs2295080, on the PI3K/AKT/mTOR signaling pathway genes are associated with genetic susceptibility to gastric cancer in Chinese population.
PI3K/AKT/mTOR信号通路的过度激活是人类癌症中最常见的变化之一,其功能区域存在的单核苷酸多态性(SNP)可影响多种癌症的发生过程。本研究旨在筛选出PI3K/AKT/mTOR信号通路中与胃癌易感性相关的SNP。
在这项病例对照研究中,筛选出PIK3CA、PIK3CB、PIK3R1、PIK3R2、PIK3R3、AKT1、AKT2、AKT3和mTOR基因启动子区域5'-UTR、外显子区域或3'-UTR中的标签SNP。通过这项病例对照研究,探讨PI3K/AKT/mTOR信号通路基因的遗传变异与中国汉族人群胃癌易感性之间的关系。
结果显示,两个位点PIK3R3 rs7536272(相加模型:OR = 1.16,95%CI = 1.01 - 1.35)和mTOR rs2295080(GG与TT比较:OR = 0.75,95%CI = 0.60 - 0.94;相加模型:OR = 0.78,95%CI = 0.66 - 0.93)的多态性与研究人群中的胃癌风险相关,且两个位点之间存在联合效应(ptrend = 0.005)。
总之,PI3K/AKT/mTOR信号通路基因上的两个位点PIK3R3 rs7536272和mTOR rs2295080的多态性与中国人群胃癌的遗传易感性相关。