|
|
Study on the correlation between single nucleotide polymorphisms of APE1 gene and clinical phenotype of hepatocellular carcinoma |
LU Xiao-hua ZHU Xiao-qing▲ YUAN Hong-xin CHU Yu-shan |
Department of Interventional Radiology, Affiliated Hospital of Nantong University, Jiangsu Province, Nantong 226001,China |
|
|
Abstract Objective To investigate the correlation between the single nucleotide polymorphisms of APE1 gene at the locus of -141T/G and 148Asp/Glu and different clinical phenotypes of hepatocellular carcinoma.Methods A total of 125 patients newly diagnosed with hepatocellular carcinoma who were hospitalized in the Interventional Radiology Department of the Affiliated Hospital of Nantong University from January 1 to December 31, 2018 were selected as the research objects to extract genomic DNA.The panel high-throughput data analysis was adopted to conduct APE1 genotyping and the correlation between each genotype and the clinical phenotype of hepatocellular carcinoma was analyzed.Results At locus -141, patients with heterozygous mutant genotype TG had an increased risk of later stage than patients with wild-type TT (OR=4.513, 95%CI:1.411-14.445, P<0.05), the patients with homozygous mutant genotype GG had an increased risk of later stage than patients with wild-type TT (OR=4.444, 95%CI:1.217-16.233, P<0.05),and the risk of later stage in patients with mutant genotype TG+GG was higher than that in patients with wild type TT (OR=4.491, 95%CI:1.457-13.848, P <0.05).There was no significant difference in the risk of stages of each genotype at locus 148 (P>0.05).At locus -141,patients with heterozygous mutant genotype TG had an increased risk of portal vein invasion compared with patients with wild-type TT (OR=3.091, 95%CI:1.019-10.064, P<0.05), the patients with homozygous mutant genotype GG had an increased risk of portal vein invasion compared with patients with wild-type TT (OR=3.789, 95%CI:1.025-14.009, P<0.05), and the risk of portal vein invasion in patients who carried the mutant genotype TG+GG was higher than that in patients with wild type TT (OR=3.302, 95%CI:1.061-10.276, P<0.05).There was no significant difference in the risk of portal vein invasion among all genotypes at locus 148 (P>0.05).There was no significant difference in the risk of lymph node metastasis among genotypes at locus -141 (P>0.05).At locus 148, patients with homozygous mutation GG had an increased risk of lymph node metastasis compared patients with wild-type TT (OR=3.500, 95%CI:1.018-12.03, P<0.05).At locus -141, patients with homozygous mutation GG had an increased risk of distant metastasis compared with patients with wild-type TT (OR=5.667, 95%CI:1.074-29.891, P<0.05).There was no significant difference in the risk of distant metastasis among all genotypes at locus 148 (P>0.05).Conclusion The single nucleotide polymorphisms of APE1 gene are correlated with clinical phenotypes of hepatocellular carcinoma such as BCLC stage,portal vein invasion, lymph node metastasis and distant metastasis.
|
|
|
|
|
[1] |
]徐燃,缪晓东.原发性肝癌的遗传流行病学探讨[J].中国处方药,2014,12(4):88.
|
[2] |
苏睿,林峻,陈鲤群,等.高通量自动化SNP 检测技术研究进展[J].中国细胞生物学学报,2019,41(7):1412-1422.
|
[10] |
惠鹏宇,倪锋,熊虎,等.APE1 基因rs1760944 多态性与前列腺癌易感性的Meta 分析[J].中国肿瘤临床与康复,2018,25(12):1443-1447.
|
[12] |
于海跃,刘正昊,崔君鹏,等.APE1 基因(Asp148Glu)多态性与结直肠癌易感性之间关系的Meta 分析[J].临床外科杂志,2017,25(10):761-764.
|
[3] |
Wu ER,Hsieh MJ,Chiang WL,et al.Association of lncRNA CCAT2 and CASC8 gene polymorphisms with hepatocellular carcinoma[J].Int J Environ Res Public Health,2019,16(16):pii:E2833.
|
[4] |
Zhang YA,Wang SL,Wen XH,et al.Association of ACYP2 and MPHOSPH6 genetic polymorphisms with the risk of hepatocellular carcinoma in chronic hepatitis B virus carriers[J].Oncotarget,2017,8(49):86 011-86 019.
|
[5] |
De Re V,Tornesello ML,De Zorzi M,et al.Clinical significance of polymorphisms in immune response genes in hepatitis C-related hepatocellular carcinoma[J].Front Microbio,2019,10:475-485.
|
[6] |
Luo YY,Zhang HP,Huang AL,et al.Association between KIF1B rs17401966 genetic polymorphism and hepatocellular carcinoma susceptibility:an updated meta-analysis[J].BMC Med Genet,2019,20(1):59-68.
|
[16] |
Mattar MM,Zekri AN,Hussein N,et al.Polymorphisms of base-excision repair genes and the hepatocarcinogenesis[J].Gene,2018,675:62-68.
|
[17] |
陆小华,朱小庆,张玉宇,等.IL-8 基因-251T/A 和+781C/T 多态性与南通地区肝细胞癌临床表型的关联研究[J].南通大学学报(医学版),2015,35(5):377-380.
|
[18] |
黄文锋,谢伟敏,王洪学,等.Holliday 交叉识别蛋白rs3771333多态性与原发性肝癌临床表型的关联研究[J].广西医科大学学报,2014,31(4):559-562.
|
[19] |
谢伟敏,翟芸,周钢桥,等.DNA 修复基因XPG His1104Asp多态性与原发性肝癌临床表型及预后的关联研究[J].中国癌症杂志,2012,22(6):458-463.
|
[7] |
Liu S,Yang TB,Nan YL,et al.Genetic variants of cell cycle pathway genes predict disease-free survival of hepatocellular carcinoma[J].Cancer Med,2017,6(7):1512-1522.
|
[8] |
Li W,Dong CW.Polymorphism in asparagine synthetase is associated with overall survival of hepatocellular carcinoma patients[J].BMC Gastroenterol,2017,17(1):79-85.
|
[9] |
Chen CT,Liao WY,Hsu CC,et al.FUT2 genetic variants as predictors of tumor development with hepatocellular carcinoma[J].Int J Med Sci,2017,14(9):885-890.
|
[11] |
Zhang SH,Wang LA,Li Z,et al.APE1 polymorphisms are associated with colorectal cancer susceptibility in Chinese Hans[J].World J Gastroenterol,2014,20(26):8700-8708.
|
[13] |
Jin F,Qian C,Qing Y,et al.Genetic polymorphism of APE1 rs1130409 can contribute to the risk of lung cancer[J].Tumour Biol,2014,35(7):6665-6671.
|
[14] |
Lai CY,Hsieh LL,Tang RP,et al.Association between polymorphisms of APE1 and OGG1 and risk of colorectal cancer in Taiwan[J].World J Gastroenterol,2016,22(12):3372-3380.
|
[15] |
Dai ZJ,Wang XJ,Kang AJ,et al.Association be tween APE1 single nucleotide polymorphism (rs1760944) and cancer risk:a Meta-analysis based on 6,419 cancer cases and 6,781 case-free controls[J].J Cancer,2014,5(3):253-259.
|
|
|
|