Institute of Molecular Biomedicine, Comenius University, Bratislava, Slovakia.
Arch Oral Biol. 2012 Dec;57(12):1651-6. doi: 10.1016/j.archoralbio.2012.09.003. Epub 2012 Oct 23.
The aetiology of oral premalignant lesions is unknown. Oxidative stress is associated with inflammation and cancerogenesis. The aim of our study was to compare salivary markers of oxidative and carbonyl stress in patients with oral premalignant lesions and age-matched healthy controls. Unstimulated saliva samples were collected from 16 patients with oral premalignant lesions (leukoplakia, lichen planus, erythroplakia) and 16 age-matched healthy controls. Biochemical analysis included measurement of thiobarbituric acid reacting substances (TBARS), advanced oxidation protein products (AOPP), advanced glycation endproducts (AGEs) and total antioxidant capacity (TAC). Salivary RNA was analyzed using real time PCR. Salivary TBARS and AGEs were significantly higher in patients than in controls. No differences were found in AOPP. TAC and expression of superoxide dismutase were lower in patients than in age-matched controls. Other analyzed transcripts (vascular endothelial growth factor, sialotransferase, neuraminidase) did not differ between patients and the control group. Markers of lipoperoxidation and carbonyl stress were increased in patients with oral premalignant lesions. Decreased antioxidant status potentially due to decreased expression of antioxidant enzymes might be responsible for these findings. Our results might point to the aetiology or pathogenesis of oral premalignant lesions as well as to the mechanism of transition to oral carcinoma.
口腔癌前病变的病因尚不清楚。氧化应激与炎症和癌症发生有关。我们的研究目的是比较口腔癌前病变患者和年龄匹配的健康对照者的唾液氧化和羰基应激标志物。从 16 例口腔癌前病变患者(白斑、扁平苔藓、红斑)和 16 例年龄匹配的健康对照者中采集非刺激性唾液样本。生化分析包括测量硫代巴比妥酸反应物质 (TBARS)、晚期氧化蛋白产物 (AOPP)、晚期糖基化终产物 (AGEs) 和总抗氧化能力 (TAC)。使用实时 PCR 分析唾液 RNA。与对照组相比,患者的唾液 TBARS 和 AGEs 显著升高。AOPP 无差异。与年龄匹配的对照组相比,患者的 TAC 和超氧化物歧化酶的表达水平较低。患者和对照组之间其他分析的转录本(血管内皮生长因子、唾液转移酶、神经氨酸酶)没有差异。口腔癌前病变患者的脂质过氧化和羰基应激标志物增加。抗氧化酶表达减少导致的抗氧化状态降低可能是这些发现的原因。我们的结果可能指向口腔癌前病变的病因或发病机制,以及向口腔癌转变的机制。