Huang Yu-Liang, Wu Jun-Rong, Fang Min, Zhao Hui-Liu, Liu Zhi-Min, Ye Jian, Huang Ling-Sha, Zhu Bo
Affiliated Tumor Hospital of Guangxi Medical University, Nanning, Guangxi, China.
Medicine (Baltimore). 2019 Apr;98(14):e15090. doi: 10.1097/MD.0000000000015090.
The aim of this study was to evaluate the effects of polymorphisms in excision repair cross-complementation group 1 (ERCC1) and alpha-fetoprotein (AFP) genes and their haplotypes on the susceptibility to hepatocellular carcinoma (HCC), and to decipher the association between single-nucleotide polymorphisms (SNPs) and clinicopathologic characteristics of HCC.Peripheral blood DNA was extracted from 206 subjects. SNaPshot technique was used for genotyping 5 SNP sites of the ERCC1 rs735482, rs1046282, rs3212948, and AFP rs737241, rs4024 genotypes. Chi-squared test and logistic regression model were used to analyze the relationship of different genotypes or haplotype and the susceptibility and clinicopathologic characteristics of HCC.The frequency of GG.GA and AA genotypes at the AFP rs737241 site in the case and control groups showed statistically significant differences (P < .05). The risk of HCC in subjects carrying mutated allele A (GA+AA) was increased by 0.543-times (P < .05) compared to that in the subjects with the GG genotype. Significant differences were observed in the linkage disequilibrium between 2 of the five SNPs (P < .05); the frequency of ERCC1 C-C and AFP A-A haplotypes was significantly lower in the case group than in the control group (P < .05). The results of clinicopathologic analysis showed that A allele at the rs737241 locus could increase the expression level of AFP (P = .007), the rs1046282 mutation C allele could increase the AFP expression level (P = .011), rs4024 locus mutation A allele could reduce the risk of vascular invasion (P = .013), rs3212948 locus mutation T allele could reduce the differentiation of liver cancer (P = .022), rs1046282 locus C allele could reduce the DNA load of hepatitis B virus (P = .035), and rs735482 A allele could increase the tumor size in HCC (P = .037).The SNPs in rs737241 for AFP gene may correlate with the occurrence of HCC. The SNPs in ERCC1 and AFP genes may affect the prognosis of HCC, offering reliable information for early prediction of tumor progression and diagnosis of HCC.
本研究旨在评估切除修复交叉互补组1(ERCC1)和甲胎蛋白(AFP)基因多态性及其单倍型对肝细胞癌(HCC)易感性的影响,并解读单核苷酸多态性(SNP)与HCC临床病理特征之间的关联。从206名受试者中提取外周血DNA。采用SNaPshot技术对ERCC1基因的rs735482、rs1046282、rs3212948以及AFP基因的rs737241、rs4024这5个SNP位点进行基因分型。采用卡方检验和逻辑回归模型分析不同基因型或单倍型与HCC易感性及临床病理特征的关系。病例组和对照组在AFP基因rs737241位点的GG、GA和AA基因型频率存在统计学显著差异(P<0.05)。携带突变等位基因A(GA+AA)的受试者患HCC的风险比GG基因型受试者增加了0.543倍(P<0.05)。五个SNP中的两个之间的连锁不平衡存在显著差异(P<0.05);病例组中ERCC1基因的C-C和AFP基因的A-A单倍型频率显著低于对照组(P<0.05)。临床病理分析结果显示,rs737241位点的A等位基因可增加AFP的表达水平(P=0.007),rs1046282位点的突变C等位基因可增加AFP表达水平(P=0.011),rs4024位点的突变A等位基因可降低血管侵犯风险(P=0.013),rs3212948位点的突变T等位基因可降低肝癌分化程度(P=0.022),rs1046282位点的C等位基因可降低乙肝病毒的DNA载量(P=0.035),rs735482位点的A等位基因可增加HCC中的肿瘤大小(P=0.037)。AFP基因rs737241位点的SNP可能与HCC的发生相关。ERCC1和AFP基因的SNP可能影响HCC的预后,为肿瘤进展的早期预测和HCC的诊断提供可靠信息。