在具有神经节胶质瘤组织学特征的神经胶质瘤中,VOPP1::EGFR融合与NFκB通路激活相关。

IF 6.2 2区 医学 Q1 NEUROSCIENCES
Max Braune, Mathias Stiller, Cordula Scherlach, Florian Wilhelmy, Katja Jähne, Wolf C Müller, Alonso Barrantes-Freer
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引用次数: 0

摘要

神经胶质瘤是由神经细胞和神经胶质瘤细胞组成的原发性脑肿瘤,通常表现为癫痫发作,主要影响儿童和年轻人。具体而言,神经节胶质瘤由肿瘤神经节细胞和胶质细胞组成,并伴有其他特征性组织学特征,如淋巴样弯曲、嗜酸性颗粒体和Rosenthal纤维。致癌驱动突变和基因融合已被证明在神经节胶质瘤中具有预后意义,并可以提供潜在的治疗靶点。典型的分子改变是丝裂原活化蛋白激酶(MAPK)途径的激活,其中BRAF p.V600E是最常见的。在这里,我们首次报道了表皮生长因子受体(EGFR)和囊泡之间的基因融合,在癌症中过度表达,促生存蛋白1 (VOPP1)在形态类似神经节胶质瘤的胶质神经元肿瘤中作为潜在的致癌驱动因素。VOPP1: EGFR融合与活化B细胞核因子κ轻链增强子(NFκB)信号通路的激活相关。此外,我们提供组织学和表观遗传学结果和临床结果。该病例扩展了已知的胶质神经元肿瘤致癌驱动因素的分子谱,并提供了潜在预后和治疗相关改变的联系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
VOPP1::EGFR fusion is associated with NFκB pathway activation in a glioneural tumor with histological features of ganglioglioma.

Glioneural tumors are primary brain tumors that consist of both neural and glial neoplastic cells, often presenting with seizures and primarily affecting children and young adults. Specifically, gangliogliomas are composed of neoplastic ganglion and glial cells, accompanied by other characteristic histological features such as lymphoid cuffing, eosinophilic granular bodies, and Rosenthal fibers. Oncogenic driver mutations and gene fusions have been shown to be of prognostic significance in gangliogliomas and can offer potential therapeutic targets. Typical molecular alterations are mitogen-activated protein kinase (MAPK) pathway activations with BRAF p.V600E being the most frequent one. Here, we report for the first time a gene fusion between epidermal growth factor receptor (EGFR) and vesicular, overexpressed in cancer, prosurvival protein 1 (VOPP1) as a potential oncogenic driver in a glioneuronal tumor morphologically resembling ganglioglioma. VOPP1::EGFR fusion associated with the activation of nuclear factor kappa-light-chain-enhancer of activated B cells (NFκB) signaling. Furthermore, we provide histological and epigenetic findings and clinical outcome. The case expands the known molecular spectrum of oncogenic drivers in glioneuronal tumors and provides a link to potentially prognostic and therapeutically relevant alterations.

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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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