Jiao Xingyuan, Wu Ying, Zhou Liansuo, He Jinyun, Yang Chonghua, Zhang Peng, Hu Ronglin, Luo Canqiao, Du Jun, Fu Jian, Shi Jinsen, He Rui, Li Dongming, Jun Wang
Department of General Surgery, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510080, China.
Department of General Surgery and Transplantation Surgery, University Hospital Duisburg-Essen, D-45122, Germany.
Sci Rep. 2015 Dec 15;5:18160. doi: 10.1038/srep18160.
The role of FEN1 genetic variants on gallstone and gallbladder cancer susceptibility is unknown. FEN1 SNPs were genotyped using the polymerase chain reaction-restriction fragment length polymorphism method in blood samples from 341 gallbladder cancer patients and 339 healthy controls. The distribution of FEN1-69G > A genotypes among controls (AA, 20.6%; GA, 47.2% and GG 32.2%) was significantly different from that among gallbladder cancer cases (AA, 11.1%; GA, 48.1% and GG, 40.8%), significantly increased association with gallbladder cancer was observed for subjects with both the FEN1-69G > A GA (OR = 1.73, 95% CI = 1.01-2.63) and the FEN1-69G > A GG (OR = 2.29, 95% CI = 1.31-3.9). The distribution of FEN1 -4150T genotypes among controls (TT, 21.8%;GT, 49.3% and GG 28.9%) was significantly different from that among gallbladder cancer cases (TT, 12.9%; GT, 48.4% and GG 38.7%), significantly increased association with gallbladder cancer was observed for subjects with both the FEN1-4150T GT(OR = 1.93, 95% CI = 1.04-2.91) and the FEN1-4150T GG(OR = 2.56, 95% CI = 1.37-5.39). A significant trend towards increased association with gallbladder cancer was observed with potentially higher-risk FEN1-69G > A genotypes (P < 0.001, χ2 trend test) and FEN14150G > T (P < 0.001, χ2 trend test) in gallstone presence but not in gallstone absence (P = 0.81, P = 0.89, respectively). In conclusion, this study revealed firstly that FEN1 polymorphisms and haplotypes are associated with gallbladder cancer risk.
FEN1基因变异对胆结石和胆囊癌易感性的作用尚不清楚。采用聚合酶链反应-限制性片段长度多态性方法,对341例胆囊癌患者和339例健康对照者的血样进行FEN1单核苷酸多态性(SNP)基因分型。FEN1 -69G>A基因型在对照组中的分布(AA,20.6%;GA,47.2%;GG,32.2%)与胆囊癌病例组中的分布(AA,11.1%;GA,48.1%;GG,40.8%)显著不同,FEN1 -69G>A GA基因型(比值比[OR]=1.73,95%可信区间[CI]=1.01 - 2.63)和FEN1 -69G>A GG基因型(OR=2.29,95%CI=1.31 - 3.9)的受试者与胆囊癌的关联显著增加。FEN1 -4150T基因型在对照组中的分布(TT,21.8%;GT,49.3%;GG,28.9%)与胆囊癌病例组中的分布(TT,12.9%;GT,48.4%;GG,38.7%)显著不同,FEN1 -4150T GT基因型(OR=1.93,95%CI=1.04 - 2.91)和FEN1 -4150T GG基因型(OR=2.56,95%CI=1.37 - 5.39)的受试者与胆囊癌的关联显著增加。在有胆结石的情况下,观察到FEN1 -69G>A基因型(P<0.001,卡方趋势检验)和FEN14150G>T(P<0.001,卡方趋势检验)与胆囊癌的关联有显著增加趋势,但在无胆结石的情况下未观察到(分别为P=0.81,P=0.89)。总之,本研究首次揭示FEN1基因多态性和单倍型与胆囊癌风险相关。