Whitehouse Jacqueline P, Howlett Meegan, Hii Hilary, Mayoh Chelsea, Wong Marie, Barahona Paulette, Ajuyah Pamela, White Christine L, Buntine Molly K, Dyke Jason M, Lee Sharon, Valvi Santosh, Stanley Jason, Andradas Clara, Carline Brooke, Kuchibhotla Mani, Ekert Paul G, Cowley Mark J, Gottardo Nicholas G, Endersby Raelene
Brain Tumour Research Program, Telethon Kids Institute, Nedlands, WA 6009, Australia.
Centre for Child Health Research, University of Western Australia, Nedlands, WA 6009, Australia.
Cancers (Basel). 2020 Oct 12;12(10):2937. doi: 10.3390/cancers12102937.
Radiation-induced glioma (RIG) is a highly aggressive brain cancer arising as a consequence of radiation therapy. We report a case of RIG that arose in the brain stem following treatment for paediatric medulloblastoma, and the development and characterisation of a matched orthotopic patient-derived xenograft (PDX) model (TK-RIG915). Patient and PDX tumours were analysed using DNA methylation profiling, whole genome sequencing (WGS) and RNA sequencing. While initially thought to be a diffuse intrinsic pontine glioma (DIPG) based on disease location, results from methylation profiling and WGS were not consistent with this diagnosis. Furthermore, clustering analyses based on RNA expression suggested the tumours were distinct from primary DIPG. Additional gene expression analysis demonstrated concordance with a published RIG expression profile. Multiple genetic alterations that enhance PI3K/AKT and Ras/Raf/MEK/ERK signalling were discovered in TK-RIG915 including an activating mutation in , upregulation of and , inactivating mutations in , and a gain-of-function mutation in . Additionally, deletion of , increased expression, and decreased expression were observed. Detection of phosphorylated S6, 4EBP1 and ERK via immunohistochemistry confirmed PI3K pathway and ERK activation. Here, we report one of the first PDX models for RIG, which recapitulates the patient disease and is molecularly distinct from primary brain stem glioma. Genetic interrogation of this model has enabled the identification of potential therapeutic vulnerabilities in this currently incurable disease.
放射性诱发胶质瘤(RIG)是一种因放射治疗而产生的高度侵袭性脑癌。我们报告了一例在小儿髓母细胞瘤治疗后发生于脑干的RIG病例,以及一个匹配的原位患者来源异种移植(PDX)模型(TK - RIG915)的建立和特征描述。使用DNA甲基化谱分析、全基因组测序(WGS)和RNA测序对患者和PDX肿瘤进行了分析。虽然最初基于疾病位置认为是弥漫性固有脑桥胶质瘤(DIPG),但甲基化谱分析和WGS的结果与该诊断不一致。此外,基于RNA表达的聚类分析表明这些肿瘤与原发性DIPG不同。额外的基因表达分析显示与已发表的RIG表达谱一致。在TK - RIG915中发现了多种增强PI3K/AKT和Ras/Raf/MEK/ERK信号传导的基因改变,包括 中的激活突变、 和 的上调、 中的失活突变以及 中的功能获得性突变。此外,还观察到 的缺失、 表达增加和 表达降低。通过免疫组织化学检测磷酸化的S6、4EBP1和ERK证实了PI3K途径和ERK的激活。在此,我们报告了首批RIG的PDX模型之一,该模型概括了患者疾病,并且在分子水平上与原发性脑干胶质瘤不同。对该模型的基因研究使得能够识别这种目前无法治愈疾病中的潜在治疗弱点。