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2015 Fiscal Year Final Research Report

Elucidation of pathogenic mechanism of schizophrenia focused on intracellular signaling by quantitative proteomics

Research Project

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Project/Area Number 26860057
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Pharmacology in pharmacy
Research InstitutionKumamoto University

Principal Investigator

Hirayama Mio  熊本大学, その他の研究科, 助教 (90706483)

Project Period (FY) 2014-04-01 – 2016-03-31
Keywordsプロテオミクス / ネットワーク解析 / 統合失調症
Outline of Final Research Achievements

We identified differentially expressed proteins in the brains of schizophrenia patients by high-precision quantitative mass spectrometric analysis. A network analysis based on protein-expression data identified a decrease in “GNA13-ERK-eIF4G2” signaling. A co-expression analysis using the protein expression levels determined by targeted proteomics was performed, whereby the signaling proteins significantly correlated between upstream and downstream proteins. These results suggest a correlation between attenuation of the molecular network involving ERK1 in the prefrontal cortex of schizophrenia patients and schizophrenia pathology.

Free Research Field

プロテオミクス

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Published: 2017-05-10  

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