Federal University of Uberlândia School of Dentistry, Area of Pathology Av. Pará, nº 1.720, CEP: 38.405-320 Uberlândia - MG, Brazil
Med Oral Patol Oral Cir Bucal. 2021 May 1;26(3):e334-e340. doi: 10.4317/medoral.24215.
Metallothioneins (MTs) gene polymorphisms have been associated with the ability of free radical scavenging and detoxification of heavy metals leading to cancer development. Our aim was to revisit, in a Brazilian population, single-nucleotide polymorphisms (SNPs) of the MT gene family previously associated with oral squamous cell carcinoma (OSCC).
A case-control investigation with 28 OSCC patients and 45 controls was conducted, using conventional risk factors (tobacco use and alcohol consumption) as covariates. SNPs genotyping for rs8052334 (MT1B), rs964372 (MT1B), and rs1610216 (MT2A) was performed by PCR-RFLP, and SNPs for rs11076161 (MT1A) were analyzed by TaqMan assay.
The only SNP associated with increased risk for OSCC was the MT-1A AA genotype (OR = 4.7; p = 0.01). We have also evidenced for the first time a significant linkage disequilibrium between the SNPs of MT-2A and MT-1A in this population with the highest frequency (30%) of the unfavorable haplotype G/A/C/T (rs1610216 / rs11076161 / rs964372 / rs8052334) of MT gene polymorphisms (OR = 6.2; p = 0.04). Interestingly, after removing the effects of conventional risk factors, we have uncovered the significance of the AA genotype of the rs11076161 with increased odds of 19-fold higher towards OSCC development.
This is the first demonstration that a significant linkage disequilibrium among gene polymorphisms of the MT family may affect susceptibility to oral cancer, which is conditioned by the G/A/C/T haplotype (rs1610216/rs11076161/rs964372/ rs8052334) and the MT-1A gene polymorphism has a potential clinical utility for the OSCC risk assessment.
金属硫蛋白(MTs)基因多态性与自由基清除和重金属解毒能力有关,从而导致癌症的发生。我们的目的是在巴西人群中重新研究先前与口腔鳞状细胞癌(OSCC)相关的 MT 基因家族的单核苷酸多态性(SNPs)。
进行了一项病例对照研究,共纳入 28 名 OSCC 患者和 45 名对照,将吸烟和饮酒等传统危险因素作为协变量。采用 PCR-RFLP 法对 rs8052334(MT1B)、rs964372(MT1B)和 rs1610216(MT2A)的 SNP 进行基因分型,采用 TaqMan 检测分析 rs11076161(MT1A)的 SNP。
唯一与 OSCC 风险增加相关的 SNP 是 MT-1A AA 基因型(OR=4.7;p=0.01)。我们还首次在该人群中发现 MT-2A 和 MT-1A 之间存在显著的连锁不平衡,该人群中最常见的不利单倍型 G/A/C/T(rs1610216/rs11076161/rs964372/rs8052334)的频率为 30%(OR=6.2;p=0.04)。有趣的是,在去除传统危险因素的影响后,我们发现 rs11076161 的 AA 基因型与 OSCC 发生的几率增加了 19 倍,这具有统计学意义。
这是首次证明 MT 家族基因多态性之间的显著连锁不平衡可能影响口腔癌的易感性,这种易感性受 G/A/C/T 单倍型(rs1610216/rs11076161/rs964372/ rs8052334)和 MT-1A 基因多态性的影响,并且对 OSCC 风险评估具有潜在的临床应用价值。