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具有原始神经元成分的胶质母细胞瘤的下一代全外显子组测序。

Next-generation whole exome sequencing of glioblastoma with a primitive neuronal component.

机构信息

Department of Pathology and Laboratory Medicine, North Shore University Hospital and Long Island Jewish Medical Center, Lake Success, 11042, NY, USA.

Department of Pathology and Laboratory Medicine, Weill Cornell Medicine College, New York, NY, 10065, USA.

出版信息

Brain Tumor Pathol. 2019 Jul;36(3):129-134. doi: 10.1007/s10014-019-00334-1. Epub 2019 Feb 4.

Abstract

Glioblastoma with a primitive neuronal component (GBM-PN) was renamed from glioblastoma with primitive neuroectodermal tumor-like component (GBM-PNET) in the new WHO classification of tumors of the central nervous system in 2016. GBM-PN is a rare variant of glioblastoma. There were not so many publications on the investigation of GBM-PN. We did whole exome sequencing for 11 GBM-PN cases and found that the percentage of TP53, PIK3CA, PIK3R1, or PTEN mutation in our GBM-PN cases (72.7%, 27.3%, 27.3%, and 27.3% respectively) was much higher than that in cases in TCGA GBM 2008, TCGA GBM 2013, and TCGA lower-grade glioma databases. The findings indicate that GBM-PN is a distinct variant of glioblastoma. The next-generation sequencing can play a role in the diagnosis of GBM-PN especially for small biopsy cases. Eight out of 11 cases showed mutations in PTEN-PI3K pathway, which indicates that targeted therapeutic agents (PI3K inhibitors, mTORC1 inhibitors or dual PI3K/mTOR inhibitors) may be used for the treatment of GBM-PN in the future.

摘要

胶质母细胞瘤伴原始神经上皮成分(GBM-PN)于 2016 年在新版《中枢神经系统肿瘤 WHO 分类》中被重新命名为胶质母细胞瘤伴原始神经外胚层肿瘤样成分(GBM-PNET)。GBM-PN 是胶质母细胞瘤的一种罕见变异型。目前关于 GBM-PN 的研究报道并不多。我们对 11 例 GBM-PN 进行了全外显子组测序,发现我们的 GBM-PN 病例中 TP53、PIK3CA、PIK3R1 或 PTEN 突变的比例(分别为 72.7%、27.3%、27.3%和 27.3%)明显高于 TCGA GBM 2008、TCGA GBM 2013 和 TCGA 低级别胶质瘤数据库中的病例。这些发现表明 GBM-PN 是胶质母细胞瘤的一种独特变异型。下一代测序技术在 GBM-PN 的诊断中可能发挥作用,尤其是对于小活检病例。11 例中有 8 例存在 PTEN-PI3K 通路突变,这表明针对该通路的靶向治疗药物(PI3K 抑制剂、mTORC1 抑制剂或双重 PI3K/mTOR 抑制剂)可能在未来用于 GBM-PN 的治疗。

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