摘要
目的:探讨纤维蛋白原(Fg)基因β链启动子区域-455 G/A与胃癌发生的相关性.方法:100例胃癌患者为观察组,与观察组年龄匹配的健康体检者100例为对照组,采集两组受检者外周静脉血,用氯仿-异丙醇法提取DNA,应用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)和HindⅢ限制性内切酶、分别检测Fgβ-455G/A位点基因型.结果:(1)对照组Fgβ-455位点等位基因G和A的频率分别为0.745、0.255,基因型分布符合Hardy-Weinberg平衡定律;(2)胃癌组Fgβ-455位点GG、GA、AA基因型频率分别为69%、29%和2%,对照组分别为57%、35%和8%,两组比较P>0.05;Fgβ-455-G、A等位基因频率在胃癌组与对照组分别为0.835、0.745和0.165、0.255,两组比较P<0.05;(3)突变纯合子AA型与胃癌的发病有关联(OR=0.842,95% CI=0.362~9.323,P=0.034),显著降低胃癌的发病风险.结论:Fgβ-455G/A位点基因多态性可能与胃癌发病有关,A等位基因可能对胃癌发病是保护性基因.
Objective: To investigate the relevance between Fibrinogen gene beta chain promoter re- gions-455 gene and gastric cancer. Methods: 100 gastric cancer patients were selected as observation group, 100 same age healthy controls as control group. Collecting peripheral venous blood of both groups, DNA was extracted by chloroform-isopropyl alcohol method. Then, adopting PCR-RFLP and Hind II[ restriction enzymes to detect gene in BB-455-g/A polymorphism loci. Results: (1)Fgβ-455 loci alleles G and A frequency were 0. 745 and O. 255 in control group, genotype distribution was con- sistent with Hardy-Weinberg equilibrium principle ; ( 2 ) Fg13-455-g gene GG, GA, AA, respectively were 69%, 29% and2% in observation group, and 57% ,35% and 8% of that of control group, com- parison differences P 〉0.05 ; (3) Fgβ-455-G, A allele were 0. 835 and 0. 745, 0. 165 and 0. 255 in both groups, comparison differences P 〈 0.05 ; (3) Homozygous mutations of AA type was relevant with the onset of gastric cancer ( OR = 0. 842 ;95 % CI was 0. 362 ~ 9. 323 ; P = 0. 034 ), which is signifi- cant in reducing the risks of gastric cancer. Conclusions: Fgβ-455 G/A polymorphism of chain pro- moter regions has potential relations with the onset of gastric cancer, A allele is possible to serve as pro- tective genes for onset of gastric cancer.
出处
《贵阳医学院学报》
CAS
2014年第3期328-332,共5页
Journal of Guiyang Medical College
基金
贵阳市科技局
筑科合同[2012103]92号
关键词
癌
胃
纤维蛋白原
β链启动子区域-455
多态性
单核甘酸
carcinoma
stomach
fibrinogen
beta chain promoter regions-455 gene
polymorphism,single nucleotide