口腔细胞学中的微小RNA-21和微小RNA-375作为口腔舌癌检测的生物标志物。
microRNA-21 and microRNA-375 from oral cytology as biomarkers for oral tongue cancer detection.
作者信息
He Qianting, Chen Zujian, Cabay Robert J, Zhang Leitao, Luan Xianghong, Chen Dan, Yu Tianwei, Wang Anxun, Zhou Xiaofeng
机构信息
Center for Molecular Biology of Oral Diseases, Department of Periodontics, College of Dentistry, University of Illinois at Chicago, Chicago, IL, USA; Department of Oral and Maxillofacial Surgery, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China.
Center for Molecular Biology of Oral Diseases, Department of Periodontics, College of Dentistry, University of Illinois at Chicago, Chicago, IL, USA.
出版信息
Oral Oncol. 2016 Jun;57:15-20. doi: 10.1016/j.oraloncology.2016.03.017. Epub 2016 Mar 31.
OBJECTIVE
We previously performed a meta-analysis of microRNA profiling studies on head and neck/oral cancer (HNOC), and identified 11 consistently dysregulated microRNAs in HNOC. Here, we evaluate the diagnostic values of these microRNAs in oral tongue squamous cell carcinoma (OTSCC) using oral cytology samples.
MATERIALS AND METHODS
The levels of 11 microRNAs were assessed in 39 oral cytology samples (19 OTSCC and 20 normal subjects), and 10 paired OTSCC and adjacent normal tissues. The predictive power of these microRNAs was analyzed by receiver operating characteristic curve (ROC) and random forest (RF) model. A classification and regression trees (CART) model was generated using miR-21 and miR-375, and further validated using both independent oral cytology validation sample set (14 OTSCC and 11 normal subjects) and tissue validation sample set (12 paired OTSCC and adjacent normal tissues).
RESULTS
Differential expression of miR-21, miR-100, miR-125b and miR-375 was validated in oral cytology training sample set. Based on the RF model, the combination of miR-21 and miR-375 was selected which provide best prediction of OTSCC. A CART model was constructed using miR-21 and miR-375, and was tested in both oral cytology and tissue validation sample sets. A sensitivity of 100% and specificity of 64% was achieved in distinguishing OTSCC from normal in the oral cytology validation set, and a sensitivity of 83% and specificity of 83% was achieved in the tissue validation set.
CONCLUSION
The utility of microRNA from oral cytology samples as biomarkers for OTSCC detection is successfully demonstrated in this study.
目的
我们之前对头颈部/口腔癌(HNOC)的微小RNA谱研究进行了荟萃分析,并在HNOC中鉴定出11种持续失调的微小RNA。在此,我们使用口腔细胞学样本评估这些微小RNA在口腔舌鳞状细胞癌(OTSCC)中的诊断价值。
材料与方法
在39份口腔细胞学样本(19例OTSCC和20例正常受试者)以及10对OTSCC及其相邻正常组织中评估了11种微小RNA的水平。通过受试者工作特征曲线(ROC)和随机森林(RF)模型分析了这些微小RNA的预测能力。使用miR-21和miR-375生成了分类与回归树(CART)模型,并使用独立的口腔细胞学验证样本集(14例OTSCC和11例正常受试者)以及组织验证样本集(12对OTSCC及其相邻正常组织)进行了进一步验证。
结果
在口腔细胞学训练样本集中验证了miR-21、miR-100、miR-125b和miR-375的差异表达。基于RF模型,选择了miR-21和miR-375的组合,其对OTSCC的预测效果最佳。使用miR-21和miR-375构建了CART模型,并在口腔细胞学和组织验证样本集中进行了测试。在口腔细胞学验证集中区分OTSCC与正常样本时,灵敏度达到100%,特异性达到64%;在组织验证集中,灵敏度为83%,特异性为83%。
结论
本研究成功证明了口腔细胞学样本中的微小RNA作为OTSCC检测生物标志物的实用性。