Laus Ana Carolina, de Paula Flavia Escremim, de Lima Marcos Alves, Carlos Carolina Dias, Gomes Izabela Natalia Faria, de Marchi Pedro, Valente Jenna Kadja Neves, Pioltini Ana Beatriz Maringolo, Miziara José Elias, da Silva Carlos Maciel, Viana Luciano de Souza, Scapulatempo-Neto Cristovam, Reis Rui Manuel
Molecular Oncology Research Center, Barretos Cancer Hospital, Antenor Duarte Villela St, 1331, Barretos, SP, 14784-400, Brazil.
Epidemiology and Biostatistics Department, Barretos Cancer Hospital, Barretos, Brazil.
Mol Biol Rep. 2019 Apr;46(2):2417-2425. doi: 10.1007/s11033-019-04702-0. Epub 2019 Feb 19.
Epidermal growth factor (EGF) and its receptor (EGFR) play an important role in lung carcinogenesis. A functional single nucleotide polymorphism (SNP) in EGF promoter region (EGF+61 A>G-rs4444903) has been associated with cancer susceptibility. Yet, in lung cancer, the EGF+61 A>G role is unclear. The aim of this study was to evaluate the risk of lung cancer associated with EGF+61 A>G SNP in the Brazilian population. For that, 669 lung cancer patients and 1104 controls were analyzed. EGF+61 A>G genotype was assessed by PCR-RFLP and TaqMan genotyping assay. Both patients and controls were in Hardy-Weinberg equilibrium. As expected, uni- and multivariate analyses showed that tobacco consumption and age were significant risk factors for lung cancer. The genotype frequencies in lung cancer patients were 27.3% of AA, 47.4% of AG and 25.3% of GG, and for controls were 25.3% of AA, 51.6% of AG and 23.1% of GG. The allele frequencies were 51.1% of A and 48.9% of G for both cases and controls. No significant differences for the three genotypes (AA, AG and GG-codominant model) were observed between cases and controls. We then grouped AG and GG (recessive model) genotypes, as well as AA and AG (dominant model), and again, no significant differences were also found. This is the largest study to explore EGF+61 A>G polymorphism association with lung cancer risk and suggests that this SNP is not a risk factor for lung cancer in the Brazilian population.
表皮生长因子(EGF)及其受体(EGFR)在肺癌发生过程中发挥着重要作用。EGF启动子区域的一个功能性单核苷酸多态性(SNP)(EGF+61 A>G-rs4444903)与癌症易感性相关。然而,在肺癌中,EGF+61 A>G的作用尚不清楚。本研究的目的是评估巴西人群中与EGF+61 A>G SNP相关的肺癌风险。为此,对669例肺癌患者和1104例对照进行了分析。通过PCR-RFLP和TaqMan基因分型检测评估EGF+61 A>G基因型。患者和对照均处于哈迪-温伯格平衡状态。正如预期的那样,单因素和多因素分析表明,吸烟和年龄是肺癌的重要危险因素。肺癌患者的基因型频率为AA型27.3%、AG型47.4%、GG型25.3%,对照的基因型频率为AA型25.3%、AG型51.6%、GG型23.1%。病例组和对照组的等位基因频率均为A 51.1%、G 48.9%。病例组和对照组在三种基因型(AA、AG和GG-共显性模型)之间未观察到显著差异。然后,我们将AG和GG(隐性模型)基因型以及AA和AG(显性模型)进行分组,同样也未发现显著差异。这是探索EGF+61 A>G多态性与肺癌风险关联的最大规模研究,表明该SNP不是巴西人群肺癌的危险因素。