Germline loss-of-function variant in the E3 ubiquitin ligase TRAF2 in a young adult patient with medulloblastoma: a case report.

IF 6.2 2区 医学 Q1 NEUROSCIENCES Acta Neuropathologica Communications Pub Date : 2024-12-20 DOI:10.1186/s40478-024-01896-8
Josh N Vo, Andrea Franson, Sebastian M Waszak, Yi-Mi Wu, Nicole Becker, Arul M Chinnaiyan, Dan R Robinson
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Abstract

We identified a rare heterozygous germline loss-of-function variant in the tumor necrosis factor receptor-associated factor 2 (TRAF2) in a young adult patient diagnosed with medulloblastoma. This variant is located within the TRAF-C domain of the E3 ubiquitin ligase protein and is predicted to diminish the binding affinity of TRAF2 to upstream receptors and associated adaptor proteins. Integrative genomics revealed a biallelic loss of TRAF2 via partial copy-neutral loss-of-heterozygosity of 9q in the medulloblastoma genome. We further performed comparative analysis with an in-house cohort of 20 medulloblastomas sequenced using the same platform, revealing an atypical molecular profile of the TRAF2-associated medulloblastoma. Our research adds to the expanding catalog of genetic tumor syndromes that increase the susceptibility of carriers to MB.

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一名年轻成年髓母细胞瘤患者E3泛素连接酶TRAF2的种系功能丧失变异:一例报告。
我们在一位被诊断为髓母细胞瘤的年轻成年患者中发现了罕见的肿瘤坏死因子受体相关因子2 (TRAF2)的杂合种系功能丧失变异。该变异位于E3泛素连接酶蛋白的TRAF-C结构域内,预计会降低TRAF2与上游受体和相关接头蛋白的结合亲和力。整合基因组学揭示了髓母细胞瘤基因组中9q杂合性的部分拷贝中性缺失导致TRAF2双等位基因缺失。我们进一步对使用相同平台测序的20个髓母细胞瘤内部队列进行了比较分析,揭示了traf2相关髓母细胞瘤的非典型分子特征。我们的研究增加了遗传肿瘤综合征的扩展目录,增加了MB携带者的易感性。
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来源期刊
Acta Neuropathologica Communications
Acta Neuropathologica Communications Medicine-Pathology and Forensic Medicine
CiteScore
11.20
自引率
2.80%
发文量
162
审稿时长
8 weeks
期刊介绍: "Acta Neuropathologica Communications (ANC)" is a peer-reviewed journal that specializes in the rapid publication of research articles focused on the mechanisms underlying neurological diseases. The journal emphasizes the use of molecular, cellular, and morphological techniques applied to experimental or human tissues to investigate the pathogenesis of neurological disorders. ANC is committed to a fast-track publication process, aiming to publish accepted manuscripts within two months of submission. This expedited timeline is designed to ensure that the latest findings in neuroscience and pathology are disseminated quickly to the scientific community, fostering rapid advancements in the field of neurology and neuroscience. The journal's focus on cutting-edge research and its swift publication schedule make it a valuable resource for researchers, clinicians, and other professionals interested in the study and treatment of neurological conditions.
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