In private oral surgery and medicine practice, Murcia, Spain.
Oral and Maxillofacial Surgery, Reina Sofia Hospital, Murcia, Spain.
Int J Dermatol. 2019 Sep;58(9):1078-1082. doi: 10.1111/ijd.14473. Epub 2019 May 21.
DNA promoter methylation is usually an early stage in carcinogenesis process, including oral cancer. The purpose of this study was to investigate the association between T allele of specific single nucleotide polymorphism (SNP) C>T rs 16906252 and O16-methylguanine-DNA methyltransferase (MGMT) methylation as prospective biomarkers of malignant transformation in oral lichen planus (OLP), a chronic autoimmune mucocutaneous disease.
This research is an observational, analytical case-control study where a total of 85 subjects (43 control individuals and 42 OLP patients) participated. The samples (mouthwashes) from all volunteers were analyzed, and DNA extraction was carried out. The genotyping of the rs 16906252 SNP in the MGMT gene was performed by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Statistical analyses of Student t test and multiple logistic regressions were used.
C>T genotype in the control and OLP groups was detected in 2.3% and 19.0%, respectively. The presence of this genotype was associated with methylation of the MGMT gene. In fact, taking into account age and gender, subjects with C>T genotype were 10.5 (95% CI 1.03-106; P = 0.047) times more likely to methylate promoter region of the MGMT gene.
These findings indicate that C>T allele of rs 16906252, predictor of MGMT promoter methylation status, may be an important feature in the clinical prognosis of premalignant lesions of OLP, although this finding requires further clinical and laboratory investigation.
DNA 启动子甲基化通常是癌症发生过程的早期阶段,包括口腔癌。本研究旨在探讨特定单核苷酸多态性(SNP)C>T rs16906252 的 T 等位基因与 O16-甲基鸟嘌呤-DNA 甲基转移酶(MGMT)甲基化之间的关联,作为口腔扁平苔藓(OLP)恶性转化的前瞻性生物标志物,OLP 是一种慢性自身免疫性粘膜疾病。
本研究是一项观察性、分析性病例对照研究,共有 85 名受试者(43 名对照组和 42 名 OLP 患者)参与。对所有志愿者的样本(漱口液)进行分析,并进行 DNA 提取。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法对 MGMT 基因 rs16906252 进行基因分型。采用 Student t 检验和多因素逻辑回归进行统计分析。
对照组和 OLP 组分别检测到 C>T 基因型的 2.3%和 19.0%。该基因型的存在与 MGMT 基因的甲基化有关。事实上,考虑到年龄和性别,携带 C>T 基因型的个体发生 MGMT 基因启动子区甲基化的可能性是 10.5 倍(95%CI 1.03-106;P=0.047)。
这些发现表明,rs16906252 的 C>T 等位基因,MGMT 启动子甲基化状态的预测因子,可能是 OLP 癌前病变临床预后的一个重要特征,尽管这一发现需要进一步的临床和实验室研究。