浙江医学
浙江醫學
절강의학
ZHEJIANG MEDICAL JOURNAL
2013年
20期
1791-1794,1801
,共5页
王黎芳%赵宏光%李昕如%伊媛琪
王黎芳%趙宏光%李昕如%伊媛琪
왕려방%조굉광%리흔여%이원기
FasL基因%单核苷酸多态性%食管癌
FasL基因%單覈苷痠多態性%食管癌
FasL기인%단핵감산다태성%식관암
FasL gene%SNP%Esophageal cancer
目的:研究FasL基因启动子区-844T/C单核苷酸多态性(SNP)与食管鳞癌易感性的关系。方法提取248例食管鳞癌患者(患者组)和297例健康体检者(对照组)外周血基因组DNA,以PCR-RFLP检测FasL-844T/CSNP。分析、比较两组该位点SNP的表达差异。结果食管鳞癌患者与健康体检者的FasL基因启动子区-844位点基因型分布差异有统计学意义(P<0.01)。以TT基因型为对照,TC基因型不增加食管鳞癌患病风险(P>0.05),而CC基因型则显著减少食管鳞癌患病风险(调整后OR=0.425,95%CI=0.255~0.708,P<0.01)。以T等位基因为对照,C等位基因显著减少食管鳞癌患病风险(调整后OR=0.597,95%CI=0.460~0.776,P<0.01)。结论在浙江地区人群中FasL基因-844T/CSNP与食管鳞癌的易感性有关。
目的:研究FasL基因啟動子區-844T/C單覈苷痠多態性(SNP)與食管鱗癌易感性的關繫。方法提取248例食管鱗癌患者(患者組)和297例健康體檢者(對照組)外週血基因組DNA,以PCR-RFLP檢測FasL-844T/CSNP。分析、比較兩組該位點SNP的錶達差異。結果食管鱗癌患者與健康體檢者的FasL基因啟動子區-844位點基因型分佈差異有統計學意義(P<0.01)。以TT基因型為對照,TC基因型不增加食管鱗癌患病風險(P>0.05),而CC基因型則顯著減少食管鱗癌患病風險(調整後OR=0.425,95%CI=0.255~0.708,P<0.01)。以T等位基因為對照,C等位基因顯著減少食管鱗癌患病風險(調整後OR=0.597,95%CI=0.460~0.776,P<0.01)。結論在浙江地區人群中FasL基因-844T/CSNP與食管鱗癌的易感性有關。
목적:연구FasL기인계동자구-844T/C단핵감산다태성(SNP)여식관린암역감성적관계。방법제취248례식관린암환자(환자조)화297례건강체검자(대조조)외주혈기인조DNA,이PCR-RFLP검측FasL-844T/CSNP。분석、비교량조해위점SNP적표체차이。결과식관린암환자여건강체검자적FasL기인계동자구-844위점기인형분포차이유통계학의의(P<0.01)。이TT기인형위대조,TC기인형불증가식관린암환병풍험(P>0.05),이CC기인형칙현저감소식관린암환병풍험(조정후OR=0.425,95%CI=0.255~0.708,P<0.01)。이T등위기인위대조,C등위기인현저감소식관린암환병풍험(조정후OR=0.597,95%CI=0.460~0.776,P<0.01)。결론재절강지구인군중FasL기인-844T/CSNP여식관린암적역감성유관。
Objective To explore the relationship between FasL gene- 844T/C single nucleotide polymorphism (SNP)in promoter and susceptibility of esophageal cancer in Zhejiang Province. Methods The clinical data of 248 patients with esophageal squamous cellcarcinoma admitted in Zhejiang Cancer Hospital from January 2008 to October 2011 were col ected and 297 healthy individuals were selected as normal controls. Genomic DNA was extracted from peripheral whole blood. PCR- RFLP technique was carried out to detect FasL- 844T/C SNP. X2 test and logistic regression was carried out for analysis. Results There was significant difference in genotypes of FasL gene promoter - 844 locus between patients and controls (P<0.05). CC genotype significantly reduced the prevalence of esophageal squamous cellcarcinoma risk(adjusted OR =0.425, 95%CI 0.255~0.708, P<0.01). Compared to T al ele, C al ele significantly reduced the prevalence of esophageal squamous cell car-cinoma risk (adjusted OR=0.597, 95%CI 0.460~0.776, P<0.01). Conclusion FasL gene- 844T/C SNP is associated with the occurrence of esophageal squamous cellcarcinoma in population of Zhejiang Province.