Suppr超能文献

伴 ATRX 改变、激酶融合及间变特征的胶质神经元肿瘤(GTAKA):一种具有复发性 NTRK 基因融合的分子上独特的脑肿瘤类型。

Glioneuronal tumor with ATRX alteration, kinase fusion and anaplastic features (GTAKA): a molecularly distinct brain tumor type with recurrent NTRK gene fusions.

机构信息

Department of Neuropathology, Institute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.

Clinical Cooperation Unit Neuropathology, German Consortium for Translational Cancer Research (DKTK), German Cancer Research Center (DKFZ), Heidelberg, Germany.

出版信息

Acta Neuropathol. 2023 May;145(5):667-680. doi: 10.1007/s00401-023-02558-0. Epub 2023 Mar 18.

Abstract

Glioneuronal tumors are a heterogenous group of CNS neoplasms that can be challenging to accurately diagnose. Molecular methods are highly useful in classifying these tumors-distinguishing precise classes from their histological mimics and identifying previously unrecognized types of tumors. Using an unsupervised visualization approach of DNA methylation data, we identified a novel group of tumors (n = 20) that formed a cluster separate from all established CNS tumor types. Molecular analyses revealed ATRX alterations (in 16/16 cases by DNA sequencing and/or immunohistochemistry) as well as potentially targetable gene fusions involving receptor tyrosine-kinases (RTK; mostly NTRK1-3) in all of these tumors (16/16; 100%). In addition, copy number profiling showed homozygous deletions of CDKN2A/B in 55% of cases. Histological and immunohistochemical investigations revealed glioneuronal tumors with isomorphic, round and often condensed nuclei, perinuclear clearing, high mitotic activity and microvascular proliferation. Tumors were mainly located supratentorially (84%) and occurred in patients with a median age of 19 years. Survival data were limited (n = 18) but point towards a more aggressive biology as compared to other glioneuronal tumors (median progression-free survival 12.5 months). Given their molecular characteristics in addition to anaplastic features, we suggest the term glioneuronal tumor with ATRX alteration, kinase fusion and anaplastic features (GTAKA) to describe these tumors. In summary, our findings highlight a novel type of glioneuronal tumor driven by different RTK fusions accompanied by recurrent alterations in ATRX and homozygous deletions of CDKN2A/B. Targeted approaches such as NTRK inhibition might represent a therapeutic option for patients suffering from these tumors.

摘要

胶质神经元肿瘤是一组异质性中枢神经系统肿瘤,准确诊断具有挑战性。分子方法在对这些肿瘤进行分类方面非常有用,可区分其与组织学模拟物的精确类别,并识别以前未被认识到的肿瘤类型。我们使用无监督的 DNA 甲基化数据可视化方法,鉴定了一组新的肿瘤(n=20),它们形成了一个与所有已建立的中枢神经系统肿瘤类型分开的聚类。分子分析显示,所有这些肿瘤均存在 ATRX 改变(16/16 例通过 DNA 测序和/或免疫组化)以及涉及受体酪氨酸激酶(RTK;主要为 NTRK1-3)的潜在靶向基因融合(16/16;100%)。此外,拷贝数谱分析显示 55%的病例存在 CDKN2A/B 的纯合缺失。组织学和免疫组织化学研究显示,这些肿瘤具有同形的、圆形的、常呈浓缩状的核,核周空晕,高有丝分裂活性和微血管增生。肿瘤主要位于幕上(84%),发生于中位年龄为 19 岁的患者。生存数据有限(n=18),但与其他胶质神经元肿瘤相比,这些肿瘤的生物学行为更具侵袭性(中位无进展生存期 12.5 个月)。鉴于其分子特征以及间变特征,我们建议使用术语 ATRX 改变、激酶融合和间变特征的胶质神经元肿瘤(glioneuronal tumor with ATRX alteration, kinase fusion and anaplastic features,GTAKA)来描述这些肿瘤。总之,我们的研究结果强调了一种新的胶质神经元肿瘤类型,由不同的 RTK 融合驱动,并伴有 ATRX 反复改变和 CDKN2A/B 的纯合缺失。针对这些肿瘤的靶向治疗方法,如 NTRK 抑制,可能是一种治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9442/10119244/8c014e69beb7/401_2023_2558_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验