School of Dental Sciences, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.
Cancer Research Centre, Institute for Medical Research, National Institutes of Health, Ministry of Health Malaysia, Setia Alam, Malaysia.
Br J Cancer. 2021 Aug;125(3):413-421. doi: 10.1038/s41416-021-01411-z. Epub 2021 May 10.
This study was undertaken to develop and validate a gene expression signature that characterises oral potentially malignant disorders (OPMD) with a high risk of undergoing malignant transformation.
Patients with oral epithelial dysplasia at one hospital were selected as the 'training set' (n = 56) whilst those at another hospital were selected for the 'test set' (n = 66). RNA was extracted from formalin-fixed paraffin-embedded (FFPE) diagnostic biopsies and analysed using the NanoString nCounter platform. A targeted panel of 42 genes selected on their association with oral carcinogenesis was used to develop a prognostic gene signature. Following data normalisation, uni- and multivariable analysis, as well as prognostic modelling, were employed to develop and validate the gene signature.
A prognostic classifier composed of 11 genes was developed using the training set. The multivariable prognostic model was used to predict patient risk scores in the test set. The prognostic gene signature was an independent predictor of malignant transformation when assessed in the test set, with the high-risk group showing worse prognosis [Hazard ratio = 12.65, p = 0.0003].
This study demonstrates proof of principle that RNA extracted from FFPE diagnostic biopsies of OPMD, when analysed on the NanoString nCounter platform, can be used to generate a molecular classifier that stratifies the risk of malignant transformation with promising clinical utility.
本研究旨在开发和验证一种基因表达特征,以识别具有高恶性转化风险的口腔潜在恶性疾病(OPMD)。
一家医院的口腔上皮异型增生患者被选为“训练集”(n=56),而另一家医院的患者被选为“测试集”(n=66)。从福尔马林固定石蜡包埋(FFPE)诊断性活检中提取 RNA,并使用 NanoString nCounter 平台进行分析。使用与口腔癌变相关的 42 个基因的靶向小组,开发了一种预后基因特征。在进行数据归一化、单变量和多变量分析以及预后建模后,开发并验证了基因特征。
使用训练集开发了由 11 个基因组成的预后分类器。在测试集中,使用多变量预后模型预测患者的风险评分。在测试集中,预后基因特征是恶性转化的独立预测因子,高风险组的预后较差[风险比=12.65,p=0.0003]。
本研究证明了从 OPMD 的 FFPE 诊断性活检中提取的 RNA,在 NanoString nCounter 平台上进行分析时,可用于生成一种分子分类器,该分类器具有有希望的临床应用价值,可以对恶性转化的风险进行分层。