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作 者:于来水[1] 潘凌子[1] 肖南[1] 梁晓华[1] 刘辉[2]
机构地区:[1]大连市血液中心,辽宁大连116001 [2]大连医科大学
出 处:《临床血液学杂志(输血与检验)》2016年第2期267-271,共5页Journal of Clinical Hematology(Blood Transfusion & Laboratory Medicine)
摘 要:目的:探讨19个短串联重复序列(STR)座位(D19S433、D5S818、D21S11、D18S51、D6S1043、D3S1358、D13S317、D7S820、D16S539、CSF1PO、Penta D、vWA、D8S1179、TPOX、Penta E、TH01、D12S391、D2S1338、FGA)基因多态性与胃肿瘤的关联。方法:利用毛细管电泳技术检测38例胃肿瘤患者19个STR座位的基因多态性并进行基因平衡(Hardy-Weinberg)分析,对照组为200例健康个体,通过统计学方法比较两组数据各位点基因频率。结果:实验组19个STR座位基因分布情况符合遗传规律,STR座位检测结果显示:实验组TH01-7、D5S818-15、D3S1358-18、D7S820-9、Penta E-23、D2S1338-19的频率显著高于对照组(P<0.05),D7S820-12、D12S391-17、D2S1338-20的频率显著低于对照组(P<0.05),Penta E座位纯合子的实际频率显著低于理论频率(P<0.05)。结论:TH01-7、D5S818-15、D3S1358-18、D7S820-9、Penta E-23、D2S1338-19 6个基因座附近可能存在胃肿瘤的易感基因,D7S820-12、D12S391-17、D2S1338-20 3个基因座附近可能存在胃肿瘤的抑制基因,Penta E座位的杂合子表现可能增加患胃肿瘤的风险。Objective:To explore the association between gastric cancer and the genetic polymorphism of 19 STR loci(D19S433,D5S818,D21S11,D18S51,D6S1043,D3S1358,D13S317,D7S820,D16S539,CSF1 PO,Penta D,vWA,D8S1179,TPOX,Penta E,TH01,D12S391,D2S1338 and FGA).Method:The capillary electrophoresis was applied to analyze 19 STR loci in 38 patients with gastric cancer and Hardy-Weinberg balance was tested.Two hundred healthy people were collected as control group.The significant differences in frequency of gene and homozygote were analyzed by statistical methods.Result:The gene distributions of 19 STR in experimental group were consistent with hereditary rules.The frequency of TH01-7,D5S818-15,D3S1358-18,D7S820-9,PentaE-23 and D2S1338-19 in the experimental group were significantly higher than those in the control group(P〈0.05),while the frequency of D7S820-12,D12S391-17 and D2S1338-20 were obviously lower(P〈0.05),and the actual frequency of homozygote at the locus PentaE was obviously lower than the theoretical frequency(P〈0.05).Conclusion:There may be predisposing genes of gastric cancer near the six loci of TH01-7,D5S818-15,D3S1358-18,D7S820-9,PentaE-23 and D2S1338-19,while there may be suppressor gene of gastric cancer near the three loci of D7S820-12,D12S391-17 and D2S1338-20,and the expression of heterozygote at the locus Penta E may increase the risk of gastric cancer.
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