通过转录组分析对zfa - rela融合的幕上室管膜瘤进行biglycan驱动的风险分层。

IF 6.2 2区 医学 Q1 NEUROSCIENCES
Konstantin Okonechnikov, David R Ghasemi, Daniel Schrimpf, Svenja Tonn, Martin Mynarek, Jan Koster, Till Milde, Tuyu Zheng, Philipp Sievers, Felix Sahm, David T W Jones, Andreas von Deimling, Stefan M Pfister, Marcel Kool, Kristian W Pajtler, Andrey Korshunov
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引用次数: 0

摘要

最近的基因组研究已经允许将颅内室管膜瘤细分为具有高度特异性临床特征和结果的分子不同组。大多数幕上室管膜瘤(ST-EPN)含有ZFTA-RELA融合,通常被认为是一种中等风险的肿瘤变体。然而,ST-EPN ZFTA-RELA的分子预测因子尚未确定。在这里,我们对80个ST-EPN ZFTA-RELA进行了基于甲基化的DNA分析和转录组RNA测序分析,研究了各种分子模式的临床意义。基于断点位置的ZFTA-RELA融合的主要类型与临床结果无显著相关性。多基因分析揭示了1892个存活相关基因,100个基因的元基因集通过反褶积分析将ST-EPN zfa - rela细分为由不同细胞亚群组成的有利和不利转录组亚型。BGN (biglycan)被确定为排名第一的生存相关基因,高BGN表达水平与生存差相关(PFS的风险比为17.85,OS的风险比为45.48;log-rank;假定值
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biglycan-driven risk stratification in ZFTA-RELA fusion supratentorial ependymomas through transcriptome profiling.

Recent genomic studies have allowed the subdivision of intracranial ependymomas into molecularly distinct groups with highly specific clinical features and outcomes. The majority of supratentorial ependymomas (ST-EPN) harbor ZFTA-RELA fusions which were designated, in general, as an intermediate risk tumor variant. However, molecular prognosticators within ST-EPN ZFTA-RELA have not been determined yet. Here, we performed methylation-based DNA profiling and transcriptome RNA sequencing analysis of 80 ST-EPN ZFTA-RELA investigating the clinical significance of various molecular patterns. The principal types of ZFTA-RELA fusions, based on breakpoint location, demonstrated no significant correlations with clinical outcomes. Multigene analysis disclosed 1892 survival-associated genes, and a metagene set of 100 genes subdivided ST-EPN ZFTA-RELA into favorable and unfavorable transcriptome subtypes composed of different cell subpopulations as detected by deconvolution analysis. BGN (biglycan) was identified as the top-ranked survival-associated gene and high BGN expression levels were associated with poor survival (Hazard Ratio 17.85 for PFS and 45.48 for OS; log-rank; p-value < 0.01). Furthermore, BGN immunopositivity was identified as a strong prognostic indicator of poor survival in ST-EPN, and this finding was confirmed in an independent validation set of 56 samples. Our results indicate that integrating BGN expression (at mRNA and/or protein level) into risk stratification models may improve ST-EPN ZFTA-RELA outcome prediction. Therefore, gene and/or protein expression analyses for this molecular marker could be adopted for ST-EPN ZFTA-RELA prognostication and may help assign patients to optimal therapies in prospective clinical trials.

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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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