Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA 02115, USA.
European Molecular Biology Laboratory, European Bioinformatics Institute, Hinxton, Cambridge CB10 1SD, UK.
Genes (Basel). 2020 Apr 2;11(4):387. doi: 10.3390/genes11040387.
The Genomics of Malignant Peripheral Nerve Sheath Tumor (GeM) Consortium is an international collaboration focusing on multi-omic analysis of malignant peripheral nerve sheath tumors (MPNSTs), the most aggressive tumor associated with neurofibromatosis type 1 (NF1). Here we present a summary of current knowledge gaps, a description of our consortium and the cohort we have assembled, and an overview of our plans for multi-omic analysis of these tumors. We propose that our analysis will lead to a better understanding of the order and timing of genetic events related to MPNST initiation and progression. Our ten institutions have assembled 96 fresh frozen NF1-related (63%) and sporadic MPNST specimens from 86 subjects with corresponding clinical and pathological data. Clinical data have been collected as part of the International MPNST Registry. We will characterize these tumors with bulk whole genome sequencing, RNAseq, and DNA methylation profiling. In addition, we will perform multiregional analysis and temporal sampling, with the same methodologies, on a subset of nine subjects with NF1-related MPNSTs to assess tumor heterogeneity and cancer evolution. Subsequent multi-omic analyses of additional archival specimens will include deep exome sequencing (500×) and high density copy number arrays for both validation of results based on fresh frozen tumors, and to assess further tumor heterogeneity and evolution. Digital pathology images are being collected in a cloud-based platform for consensus review. The result of these efforts will be the largest MPNST multi-omic dataset with correlated clinical and pathological information ever assembled.
恶性外周神经鞘瘤(GeM)基因组联盟是一个国际合作组织,专注于恶性外周神经鞘瘤(MPNST)的多组学分析,MPNST 是与神经纤维瘤病 1 型(NF1)相关的最具侵袭性的肿瘤。在这里,我们总结了当前的知识空白,描述了我们的联盟和我们所组建的队列,以及我们对这些肿瘤进行多组学分析的计划概述。我们提出,我们的分析将有助于更好地理解与 MPNST 起始和进展相关的遗传事件的顺序和时间。我们的十个机构已经收集了 86 名受试者的 96 份新鲜冷冻的 NF1 相关(63%)和散发性 MPNST 标本,以及相应的临床和病理数据。临床数据是作为国际 MPNST 登记处的一部分收集的。我们将用全基因组测序、RNAseq 和 DNA 甲基化谱分析来描述这些肿瘤。此外,我们将对 9 名 NF1 相关 MPNST 患者的部分肿瘤进行多区域分析和时间采样,使用相同的方法,以评估肿瘤异质性和癌症演变。随后,将对其他存档标本进行额外的多组学分析,包括深度外显子组测序(500×)和高密度拷贝数阵列,以验证基于新鲜冷冻肿瘤的结果,并进一步评估肿瘤异质性和演变。数字病理学图像正在基于云的平台中进行收集,以便进行共识审查。这些努力的结果将是有史以来收集到的具有相关临床和病理信息的最大 MPNST 多组学数据集。