Ferlazzo Nadia, Currò Monica, Zinellu Angelo, Caccamo Daniela, Isola Gaetano, Ventura Valeria, Carru Ciriaco, Matarese Giovanni, Ientile Riccardo
Department of Biomedical and Dental Sciences and Morphofunctional Imaging, University of Messina, 98124 Messina, Italy.
Department of Biomedical Sciences, University of Sassari, 07100 Sassari, Italy.
Int J Mol Sci. 2017 Mar 29;18(4):724. doi: 10.3390/ijms18040724.
Genetic polymorphisms of the methylenetetrahydrofolate reductase (MTHFR) enzyme may influence DNA methylation. Alterations in DNA methylation patterns of genes involved in the regulation of the cell cycle, DNA repair, cell adherence and metastasis process are known to contribute to cancer development. In this study, the influence of the MTHFR C677T and A1298C gene polymorphisms on global DNA methylation and site-specific methylation on and ⁶-methylguanine-DNA methyltransferase () gene promoters was investigated in patients with oral squamous cell cancer (OSCC). To this aim, methylation studies were carried out by using genomic DNA isolated from saliva samples of 58 OSCC patients and 90 healthy controls. The frequency of the CT/AC and TT/AA genotypes was significantly higher in patients than in controls. Whereas no difference in global DNA methylation levels was observed between patients and controls, a higher frequency of methylation at both and gene promoters was detected in patients compared with controls. A significant association between gene polymorphisms and and gene promoter methylation was found. The frequency of and methylation was around 60% in patients with either the CT/AC or TT/AA genotype. Our results suggest that hypermethylation of cancer-related genes may be affected by polymorphisms.
亚甲基四氢叶酸还原酶(MTHFR)的基因多态性可能会影响DNA甲基化。已知参与细胞周期调控、DNA修复、细胞黏附和转移过程的基因的DNA甲基化模式改变会促进癌症发展。在本研究中,我们调查了口腔鳞状细胞癌(OSCC)患者中亚甲基四氢叶酸还原酶C677T和A1298C基因多态性对全基因组DNA甲基化以及O⁶-甲基鸟嘌呤-DNA甲基转移酶(MGMT)基因启动子位点特异性甲基化的影响。为此,我们使用从58例OSCC患者和90例健康对照者的唾液样本中分离出的基因组DNA进行了甲基化研究。患者中CT/AC和TT/AA基因型的频率显著高于对照组。虽然患者和对照组之间未观察到全基因组DNA甲基化水平的差异,但与对照组相比,患者中MGMT和RASSF1A基因启动子的甲基化频率更高。我们发现MTHFR基因多态性与MGMT和RASSF1A基因启动子甲基化之间存在显著关联。CT/AC或TT/AA基因型的患者中,MGMT和RASSF1A甲基化频率约为60%。我们的结果表明,癌症相关基因的高甲基化可能受MTHFR多态性影响。