Faculty of Biological Sciences, Universidad Autónoma de Nuevo León, Monterrey, México.
Faculty of Public Health and Nutrition, Universidad Autónoma de Nuevo León, Monterrey, México.
Toxicol Mech Methods. 2021 Jun;31(5):343-348. doi: 10.1080/15376516.2020.1862379. Epub 2021 Jan 4.
Oral squamous cell carcinoma (OSCC) is characterized by increased genetic instability as an essential variable of event of neoplastic transformation. The aim of this study was to evaluate genomic instability in exfoliated cells from the buccal mucosa of patients with OSCC . the control group, using DNA Breakage Detection/Fluorescence hybridization (DBD-FISH). Exfoliated cells from the buccal mucosa were obtained from 38 patients with oral cancer () and from 10 individuals without oral lesions (). DNA damage was evaluated by DBD-FISH using the whole-genome DNA probe and digital imaging analysis. Collaterally, HPV infection was determined utilizing the INNO-LiPA HPV kit. Patients with OSCC showed an increase in the hybridization signal five times more intense than that of the baseline level of DNA damage detected in control individuals. The best cutoff value for predicting oral squamous cell carcinoma was 67.46, and an Odds Ratio (OR) value of 87. HPV detection analysis revealed than one patient with OSCC (2.6%) was positive for HPV. All controls were negative HPV. In conclusion, DBD-FISH permitted the clear visualization of level high of DNA damage in the buccal epithelial cells of patients with OSSC respect to control group. Chromosome instability in oral mucosa may be an individual marker of malignant transformation in OSCC.
口腔鳞状细胞癌(OSCC)的特征是遗传不稳定性增加,这是肿瘤转化事件的一个重要变量。本研究旨在评估口腔 OSCC 患者口腔颊黏膜脱落细胞的基因组不稳定性。使用 DNA 断裂检测/荧光杂交(DBD-FISH)方法对 38 名口腔癌患者(病例组)和 10 名无口腔病变者(对照组)的颊黏膜脱落细胞进行检测。通过 DBD-FISH 方法,使用全基因组 DNA 探针和数字成像分析评估 DNA 损伤。同时,利用 INNO-LiPA HPV 试剂盒检测 HPV 感染。与对照组相比,OSCC 患者的杂交信号强度增加了五倍,超过了 DNA 损伤的基线水平。预测口腔鳞状细胞癌的最佳截断值为 67.46,优势比(OR)值为 87。HPV 检测分析显示,1 例 OSCC 患者(2.6%)HPV 阳性,所有对照组均为 HPV 阴性。总之,DBD-FISH 方法能够清晰地观察到 OSCC 患者口腔颊黏膜上皮细胞中高水平的 DNA 损伤,而对照组则没有。口腔黏膜的染色体不稳定性可能是 OSCC 恶性转化的个体标志物。