广西医学
廣西醫學
엄서의학
GUANGXI MEDICAL JOURNAL
2014年
3期
277-280
,共4页
程小伟%姜力%陈静珊%张勇
程小偉%薑力%陳靜珊%張勇
정소위%강력%진정산%장용
鼻咽癌%血管内皮生长因子%单核苷酸多态性%EB病毒
鼻嚥癌%血管內皮生長因子%單覈苷痠多態性%EB病毒
비인암%혈관내피생장인자%단핵감산다태성%EB병독
Nasopharyngeal carcinoma%Vascular endothelial growth factor%Single nucleotide polymorphism%EB virus
目的:探讨广西人群中鼻咽癌的发病与VEGF-1154 G/A基因多态性、EB病毒的交互作用。方法选择鼻咽癌的患者197例为病例组,另选择在体检中心进行体检的健康人群197例为对照组,采用病例-对照研究方法分析鼻咽癌发病与VEGF-1154 G/A基因多态性、EB病毒的交互作用。结果 VEGF-1154基因型GG、GA+AA在病例组中的频率分别为40.0%、60.0%,在对照组中的频率为55.8%、44.2%,差异有统计学意义(P<0.05)。等位基因A在病例组中的分布(40.4%)明显高于对照组(26.9%)(P<0.05),与等位基因G相比,携带有等位基因A的基因型可增加鼻咽癌的发病风险( P<0.05)。但VEGF-1154等位基因A与EB-VCA-IgA、肿瘤家族史在鼻咽癌的发病过程中无交互作用( P>0.05)。结论 VEGF-1154等位基因A是鼻咽癌发生的风险因素,但其与EB病毒感染、肿瘤家族史在鼻咽癌的发生过程中无交互作用。
目的:探討廣西人群中鼻嚥癌的髮病與VEGF-1154 G/A基因多態性、EB病毒的交互作用。方法選擇鼻嚥癌的患者197例為病例組,另選擇在體檢中心進行體檢的健康人群197例為對照組,採用病例-對照研究方法分析鼻嚥癌髮病與VEGF-1154 G/A基因多態性、EB病毒的交互作用。結果 VEGF-1154基因型GG、GA+AA在病例組中的頻率分彆為40.0%、60.0%,在對照組中的頻率為55.8%、44.2%,差異有統計學意義(P<0.05)。等位基因A在病例組中的分佈(40.4%)明顯高于對照組(26.9%)(P<0.05),與等位基因G相比,攜帶有等位基因A的基因型可增加鼻嚥癌的髮病風險( P<0.05)。但VEGF-1154等位基因A與EB-VCA-IgA、腫瘤傢族史在鼻嚥癌的髮病過程中無交互作用( P>0.05)。結論 VEGF-1154等位基因A是鼻嚥癌髮生的風險因素,但其與EB病毒感染、腫瘤傢族史在鼻嚥癌的髮生過程中無交互作用。
목적:탐토엄서인군중비인암적발병여VEGF-1154 G/A기인다태성、EB병독적교호작용。방법선택비인암적환자197례위병례조,령선택재체검중심진행체검적건강인군197례위대조조,채용병례-대조연구방법분석비인암발병여VEGF-1154 G/A기인다태성、EB병독적교호작용。결과 VEGF-1154기인형GG、GA+AA재병례조중적빈솔분별위40.0%、60.0%,재대조조중적빈솔위55.8%、44.2%,차이유통계학의의(P<0.05)。등위기인A재병례조중적분포(40.4%)명현고우대조조(26.9%)(P<0.05),여등위기인G상비,휴대유등위기인A적기인형가증가비인암적발병풍험( P<0.05)。단VEGF-1154등위기인A여EB-VCA-IgA、종류가족사재비인암적발병과정중무교호작용( P>0.05)。결론 VEGF-1154등위기인A시비인암발생적풍험인소,단기여EB병독감염、종류가족사재비인암적발생과정중무교호작용。
Objective To explore the association of development of nasopharyngeal carcinoma in Guangxi population with VEGF-1154G/A gene polymorphism and EB virus .Methods One hundred and ninety-seven patients with nasopharyngeal carcinoma were in the case group ,197 healthy people in the control group .A case-control study was applied to analyzing the association of development of nasopharyngeal carcinoma with VEGF -1154G/A gene polymorphisms and EB virus . Results The distributions of VEGF-1154 GG(40.0%) and GA+AA(60.0%) in the case group differed from those (55.8%,44.2%) in healthy controls(P<0.05).Compared with the control (26.9%),the frequency of A allele in the case group(40.4%) was significantly higher (P<0.05).The genotype G/A or A/A containing A allele in contrast to genotype G/G increased the risk of nasopharyngeal carcinoma (P<0.05).However,there were no interactions among VEGF-1154 A allele ,EB-VCA-IgA and family history of cancer in the process of occurrence of nasopharyngeal carcinoma (P>0.05).Conclusion VEGF-1154 A allele is a risk factor of nasopharyngeal carcinoma ,but there are no interactions among VEGF-1154 A allele,EB-VCA-IgA and family history of cancer in the process of occurrence of nasopharyngeal carcinoma .