Department of Oral and Maxillofacial Surgery, Hospital Universitario Central de Asturias and Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), 33011 Oviedo, Asturias, Spain.
Department of Otolaryngology, Hospital Universitario Central de Asturias and Instituto de Investigación Sanitaria del Principado de Asturias (ISPA), 33011 Oviedo, Asturias, Spain.
Int J Mol Sci. 2023 Sep 21;24(18):14382. doi: 10.3390/ijms241814382.
The aim of this study was to evaluate the expression of the senescence markers, Decoy Receptor 2 (DcR2) and Differentiated Embryo-Chondrocyte expressed gen 1 (DEC1), in oral potentially malignant disorders (OPMDs) to ascertain their possible association with oral cancer risk. The immunohistochemical analysis of DcR2 and DEC1 expression (along with p16 and Ki67 expression) was carried out in 60 patients with clinically diagnosed oral leukoplakia. Fifteen cases (25%) subsequently developed an invasive carcinoma. Correlations between protein marker expression, histological grade and oral cancer risk were assessed. DcR2, DEC1 and Ki67 protein expressions were found to correlate significantly with increased oral cancer risk, and also with an increased grade of dysplasia. Multivariate analysis demonstrated that DcR2 and Ki67 expression are independent predictors of oral cancer development. Our results evidence for the first time the potential of DcR2 as an early biomarker to assess oral cancer risk in patients with oral leukoplakia (HR = 59.7, = 0.015), showing a superior predictive value to histology (HR = 4.225, = 0.08). These findings reveal that the increased expression of DcR2 and DEC1 occurred frequently in OPMDs. In addition, DcR2 expression emerges as a powerful biomarker for oral cancer risk assessment in patients with oral leukoplakia.
本研究旨在评估衰老标志物——诱饵受体 2(DcR2)和分化胚胎软骨细胞表达基因 1(DEC1)在口腔潜在恶性疾病(OPMDs)中的表达,以确定它们与口腔癌风险的可能关联。对 60 例临床诊断为口腔白斑的患者进行了 DcR2 和 DEC1 表达(以及 p16 和 Ki67 表达)的免疫组织化学分析。其中 15 例(25%)随后发展为浸润性癌。评估了蛋白标志物表达、组织学分级与口腔癌风险之间的相关性。结果发现,DcR2、DEC1 和 Ki67 蛋白表达与口腔癌风险增加显著相关,与异型增生程度增加也相关。多变量分析表明,DcR2 和 Ki67 表达是口腔癌发生的独立预测因子。本研究首次证明了 DcR2 作为评估口腔白斑患者口腔癌风险的早期生物标志物的潜力(HR = 59.7, = 0.015),其预测价值优于组织学(HR = 4.225, = 0.08)。这些发现表明,DcR2 和 DEC1 的表达增加在 OPMDs 中经常发生。此外,DcR2 表达可作为口腔白斑患者口腔癌风险评估的有力生物标志物。