Suppr超能文献

BRAF V600E 突变相关致痫性低级别神经上皮肿瘤的转录特征。

Transcriptional features of low-grade neuroepithelial tumors with the BRAF V600E mutation associated with epileptogenicity.

机构信息

Department of Neurosurgery, National Center Hospital, National Center of Neurology and Psychiatry, Kodaira, Tokyo, Japan.

Department of Biochemistry and Cellular Biology, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Kodaira, Tokyo, Japan.

出版信息

Genes Cells. 2024 Mar;29(3):192-206. doi: 10.1111/gtc.13096. Epub 2024 Jan 25.

Abstract

Low-grade neuroepithelial tumors are major causes of drug-resistant focal epilepsy. Clinically, these tumors are defined as low-grade epilepsy-associated neuroepithelial tumors (LEATs). The BRAF V600E mutation is frequently observed in LEAT and linked to poor seizure outcomes. However, its molecular role in epileptogenicity remains elusive. To understand the molecular mechanism underlying the epileptogenicity in LEAT with the BRAF V600E genetic mutation (BRAF V600E-LEAT), we conducted RNA sequencing (RNA-seq) analysis using surgical specimens of BRAF V600E-LEAT obtained and stored at a single institute. We obtained 21 BRAF V600E-LEAT specimens and 4 control specimens, including 24 from Japanese patients and 1 from a patient of Central Asian origin, along with comprehensive clinical data. We submitted the transcriptome dataset of 21 BRAF V600E-LEAT plus 4 controls, as well as detailed clinical information, to a public database. Preliminary bioinformatics analysis using this dataset identified 2134 differentially expressed genes between BRAF V600E-LEAT and control. Additionally, gene set enrichment analysis provided novel insights into the association between estrogen response-related pathways and the epileptogenicity of BRAF V600E-LEAT patients. Our datasets and findings will contribute toward the understanding of the pathology of epilepsy caused by LEAT and the identification of new therapeutic targets.

摘要

低级别神经上皮肿瘤是导致药物难治性局灶性癫痫的主要原因。临床上,这些肿瘤被定义为低级别与癫痫相关的神经上皮肿瘤(LEAT)。BRAF V600E 突变在 LEAT 中频繁出现,与较差的癫痫发作结局相关。然而,其在致痫性中的分子作用仍不清楚。为了了解具有 BRAF V600E 基因突变(BRAF V600E-LEAT)的 LEAT 致痫性的分子机制,我们使用单一机构获得和保存的 BRAF V600E-LEAT 手术标本进行了 RNA 测序(RNA-seq)分析。我们获得了 21 例 BRAF V600E-LEAT 标本和 4 例对照标本,包括来自日本的 24 例和来自中亚的 1 例,以及全面的临床数据。我们将 21 例 BRAF V600E-LEAT 加 4 例对照的转录组数据集以及详细的临床信息提交给了一个公共数据库。使用该数据集进行的初步生物信息学分析确定了 BRAF V600E-LEAT 与对照之间的 2134 个差异表达基因。此外,基因集富集分析为雌激素反应相关途径与 BRAF V600E-LEAT 患者致痫性之间的关联提供了新的见解。我们的数据集和发现将有助于理解由 LEAT 引起的癫痫病理,并确定新的治疗靶点。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验