首页 | 本学科首页   官方微博 | 高级检索  
     

多个单核苷酸多态性位点与食管癌和胃癌患病风险的相关性分析
引用本文:黄建新,李馨,王瑜,鲁朝敏. 多个单核苷酸多态性位点与食管癌和胃癌患病风险的相关性分析[J]. 重庆医学, 2018, 0(14): 1889-1895. DOI: 10.3969/j.issn.1671-8348.2018.14.013
作者姓名:黄建新  李馨  王瑜  鲁朝敏
作者单位:平顶山学院医学院护理系,河南平顶山,467000河南省肿瘤医院外科,郑州,450000
基金项目:河南省科技计划资助项目(51010205)
摘    要:目的 探讨多个单核苷酸多态性与食管癌和胃癌的关系,寻找在中国河南省汉族人群中食管癌和胃癌的共同遗传风险位点.方法 选择河南省肿瘤医院收治的食管癌患者500例,胃癌患者和健康体检者各600例,挑选了7个单核苷酸多态性(SNP)位点,采用Sequenom MassARRAY SNP基因分型技术进行基因分型.通过无条件逻辑回归计算相对优势比(OR)及其95%的置信区间(95%CI).结果 在等位基因模型下,有2个SNP位点与食管癌的患病风险相关,分别是rs4785204(OR=1.43,95%CI:1.12~1.85,P=0.01)和rs4924935位点(OR=o.76,95%CI:0.61~0.99,P=0.04).有4个SNP位点与胃癌的患病风险相关,分别是rs13361707(OR=1.23,95%CI.1.13~1.56,P=0.00)、rs4779584(OR=1.25,95%CI.1.11~1.58,P=0.04)、rs4785204(OR=1.24,95%CI:1.03~1.49,P=0.03)和rs4924935位点(OR=0.76,95%CI:0.60~0.99,P=0.04).在遗传模型分析中,发现有4个位点与食管癌的患病风险明显相关(P<0.05),分别是rs6687758、rs401681、rs4785204和rs4924935位点;有3个位点与胃癌的患病风险相关(P<0.05),分别是rs13361707、rs4779584和rs4785204位点.结论 中国河南省汉族人群中多个SNP位点与食管癌和胃癌的遗传易感性有关联,rs4785204和rs4924935位点的遗传变异可能同时在食管癌和胃癌的发生、发展中起到重要作用.

关 键 词:食管肿瘤  胃肿瘤  多态性  单核苷酸  疾病遗传易感性  esophageal neoplasms  stomach neoplasms  polymorphism,single nucleotide  genetic predisposition to disease

Analysis on correlation between multiple single nucleotide polymorphisms loci and risk of esophageal and gastric cancer
HUANG Jianxin,LI Xin,WANG Yu,LU Chaomin. Analysis on correlation between multiple single nucleotide polymorphisms loci and risk of esophageal and gastric cancer[J]. Chongqing Medical Journal, 2018, 0(14): 1889-1895. DOI: 10.3969/j.issn.1671-8348.2018.14.013
Authors:HUANG Jianxin  LI Xin  WANG Yu  LU Chaomin
Abstract:Objective To investigate the association between multiple single nucleotide polymorphisms (SNP) with esophageal and gastric cancer,and to search the shared genetic risk loci for esophageal and gastric cancer in Han population of Henan Province.Methods Five hundreds cases of esophageal cancer,600 cases of gastric cancer and 600 persons undergoing physical examination in the Henan Provincial Tumor Hospital were selected.Seven SNP loci were selected.The genotyping was performed by adopting the Sequenom MassAR-RAY SNP genoting technique.The relative odds ratios(OR) and 95 % confidence intervals(CI) were calculated by unconditional logistic regression.Results In allelic model,the two SNP loci were correlated with the risk of esophageal cancer,which were rs4785204 (OR =1.43,95 % CI:1.12-1.85,P =0.01) and rs4924935 (OR =0.76,95 %CI:0.61-0.99,P=0.04).The four SNP loci were correlated with the risk of gastric cancer,gastric cancer,which were rs13361707(OR=1.23,95%CI:1.13-1.56,P=0.00),rs4779584(OR=1.25,95%CI:1.11-1.58,P=0.04),rs4785204(OR=1.24,95%CI:1.03-1.49,P=0.03)and rs4924935(OR=0.76,95% CI:0.60-0.99,P =0.04).In the genetic model analysis,the four loci were significantly correlated with the risk of esophageal cancer,which were rs6687758,rs401681,rs4785204 and rs4924935(P<0.05);the three loci were correlated with the gastric cancer,which were rs13361707,rs4779584 and rs4785204(P<0.05).Conclusion Multiple SNP loci have the relationship with the risk of esophageal and gastric cancer in Han population of Henan Province.The genetic variation of rs4785204 and rs4924935 loci may simultaneously play an important role in the occurrence and development of esophageal and gastric cancer.
Keywords:
本文献已被 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号