Department of Pathomorphology, The Children's Memorial Health Institute, Warsaw, Poland.
Department of Experimental and Clinical Neuropathology, Mossakowski Medical Research Institute, Polish Academy of Sciences, Warsaw, Poland.
J Pathol Clin Res. 2021 Nov;7(6):565-576. doi: 10.1002/cjp2.236. Epub 2021 Jul 27.
The majority of supratentorial ependymomas in children contain oncogenic fusions, such as ZFTA-RELA or YAP1-MAMLD1. In contrast, posterior fossa (PF) ependymomas lack recurrent somatic mutations and are classified based on gene expression or methylation profiling into group A (PFA) and group B (PFB). We have applied a novel method, NanoString nCounter Technology, to identify four molecular groups among 16 supratentorial and 50 PF paediatric ependymomas, using 4-5 group-specific signature genes. Clustering analysis of 16 supratentorial ependymomas revealed 9 tumours with a RELA fusion-positive signature (RELA+), 1 tumour with a YAP1 fusion-positive signature (YAP1+), and 6 not-classified tumours. Additionally, we identified one RELA+ tumour among historically diagnosed CNS primitive neuroectodermal tumour samples. Overall, 9 of 10 tumours with the RELA+ signature possessed the ZFTA-RELA fusion as detected by next-generation sequencing (p = 0.005). Similarly, the only tumour with a YAP1+ signature exhibited the YAP1-MAMLD1 fusion. Among the remaining unclassified ependymomas, which did not exhibit the ZFTA-RELA fusion, the ZFTA-MAML2 fusion was detected in one case. Notably, among nine ependymoma patients with the RELA+ signature, eight survived at least 5 years after diagnosis. Clustering analysis of PF tumours revealed 42 samples with PFA signatures and 7 samples with PFB signatures. Clinical characteristics of patients with PFA and PFB ependymomas corroborated the previous findings. In conclusion, we confirm here that the NanoString method is a useful single tool for the diagnosis of all four main molecular groups of ependymoma. The differences in reported survival rates warrant further clinical investigation of patients with the ZFTA-RELA fusion.
儿童幕上室管膜瘤多数含有致癌融合,如 ZFTA-RELA 或 YAP1-MAMLD1。相比之下,后颅窝(PF)室管膜瘤缺乏复发性体细胞突变,并根据基因表达或甲基化谱分为 A 组(PFA)和 B 组(PFB)。我们应用一种新的方法,即 NanoString nCounter 技术,通过 4-5 个组特异性标志基因,在 16 例幕上和 50 例 PF 儿童室管膜瘤中鉴定出 4 个分子群。对 16 例幕上室管膜瘤的聚类分析显示,有 9 例肿瘤具有 RELA 融合阳性特征(RELA+),1 例肿瘤具有 YAP1 融合阳性特征(YAP1+),6 例未分类肿瘤。此外,我们还在历史上诊断的中枢神经系统原始神经外胚层肿瘤样本中鉴定出一个 RELA+肿瘤。总体而言,具有 RELA+特征的 10 个肿瘤中有 9 个通过下一代测序检测到 ZFTA-RELA 融合(p=0.005)。同样,唯一具有 YAP1+特征的肿瘤表现出 YAP1-MAMLD1 融合。在其余未分类的室管膜瘤中,未检测到 ZFTA-RELA 融合的情况下,在 1 例中检测到 ZFTA-MAML2 融合。值得注意的是,在具有 RELA+特征的 9 名室管膜瘤患者中,有 8 名在诊断后至少存活 5 年。PF 肿瘤的聚类分析显示,有 42 例具有 PFA 特征,7 例具有 PFB 特征。PFA 和 PFB 室管膜瘤患者的临床特征证实了之前的发现。总之,我们在此证实,NanoString 方法是诊断所有 4 种主要室管膜瘤分子群的有用工具。报告的生存率差异表明需要进一步对具有 ZFTA-RELA 融合的患者进行临床研究。