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

Author:

Iijima Keiya1,Komatsu Kanako2,Miyashita Satoshi2,Suyama Kyoka2,Murayama Kumiko3,Hashizume Koichi2,Tabe Nao K.2,Miyata Hajime4,Iwasaki Masaki1,Taya Shinichiro25,Hoshino Mikio2ORCID

Affiliation:

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

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

3. Medical Genome Center National Center of Neurology and Psychiatry Kodaira Tokyo Japan

4. Department of Neuropathology Research Institute for Brain and Blood Vessels, Akita Cerebrospinal and Cardiovascular Center Akita City Akita Japan

5. Division of Behavioral Neuropharmacology, International Center for Brain Science (ICBS) Fujita Health University Toyoake Aichi Japan

Abstract

AbstractLow‐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.

Funder

National Center of Neurology and Psychiatry

Uehara Memorial Foundation

Japan Health Research Promotion Bureau

Japan Society for the Promotion of Science

Japan Agency for Medical Research and Development

Publisher

Wiley

Subject

Cell Biology,Genetics

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