Department of Neurosurgery, Juntendo University Faculty of Medicine, 2-1-1 Hongo, Bunkyo-Ku, Tokyo, 113-8421, Japan.
Department of Brain Disease Translational Research, Graduate School of Medicine, Juntendo University, Tokyo, Japan.
Brain Tumor Pathol. 2023 Apr;40(2):93-100. doi: 10.1007/s10014-023-00450-z. Epub 2023 Feb 14.
The World Health Organization Classification of Tumors of the Central Nervous System 5th Edition (WHO CNS5) introduced a newly defined astrocytoma, IDH-mutant grade 4, for adult diffuse glioma classification. One of the diagnostic criteria is the presence of a CDKN2A/B homozygous deletion (HD). Here, we report a robust and cost-effective quantitative polymerase chain reaction (qPCR)-based test for assessing CDKN2A HD. A TaqMan copy number assay was performed using a probe located within CDKN2A. The linear correlation between the Ct values and relative CDKN2A copy number was confirmed using a serial mixture of DNA from normal blood and U87MG cells. The qPCR assay was performed in 109 IDH-mutant astrocytomas, including 14 tumors with CDKN2A HD, verified either by multiplex ligation-dependent probe amplification (MLPA) or CytoScan HD microarray platforms. Receiver operating characteristic curve analysis indicated that a cutoff value of 0.85 yielded optimal sensitivity (100%) and specificity (99.0%) for determining CDKN2A HD. The assay applies to DNA extracted from frozen or formalin-fixed paraffin-embedded tissue samples. Survival was significantly shorter in patients with than in those without CDKN2A HD, assessed by either MLPA/CytoScan or qPCR. Thus, our qPCR method is clinically applicable for astrocytoma grading and prognostication, compatible with the WHO CNS5.
世界卫生组织中枢神经系统肿瘤分类第五版(WHO CNS5)为成人弥漫性神经胶质瘤分类引入了一种新定义的星形细胞瘤,即 IDH 突变型 4 级。其诊断标准之一是存在 CDKN2A/B 纯合缺失(HD)。在此,我们报告了一种用于评估 CDKN2A HD 的可靠且具有成本效益的定量聚合酶链反应(qPCR)检测方法。使用位于 CDKN2A 内的探针进行 TaqMan 拷贝数测定。通过正常血液和 U87MG 细胞的 DNA 系列混合物证实了 Ct 值与相对 CDKN2A 拷贝数之间的线性相关性。在 109 例 IDH 突变型星形细胞瘤中进行了 qPCR 检测,其中包括 14 例经多重连接依赖性探针扩增(MLPA)或 CytoScan HD 微阵列平台验证的 CDKN2A HD 肿瘤。受试者工作特征曲线分析表明,0.85 的截止值可获得最佳的 CDKN2A HD 检测灵敏度(100%)和特异性(99.0%)。该检测方法适用于从冷冻或福尔马林固定石蜡包埋组织样本中提取的 DNA。通过 MLPA/CytoScan 或 qPCR 评估,CDKN2A HD 患者的生存时间明显短于无 CDKN2A HD 患者。因此,我们的 qPCR 方法在星形细胞瘤分级和预后评估方面具有临床适用性,与 WHO CNS5 一致。