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Proteomics as a Tool for Understanding Schizophrenia

Schizophrenia is likely to be a multifactorial disorder, consequence of alterations in gene and protein expression since the neurodevelopment that together to environmental factors will trigger the establishment of the disease. In the post-genomic era, proteomics has emerged as a promising strategy...

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Autor principal: Martins-de-Souza, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean College of Neuropsychopharmacology 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569116/
https://www.ncbi.nlm.nih.gov/pubmed/23430140
http://dx.doi.org/10.9758/cpn.2011.9.3.95
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author Martins-de-Souza, Daniel
author_facet Martins-de-Souza, Daniel
author_sort Martins-de-Souza, Daniel
collection PubMed
description Schizophrenia is likely to be a multifactorial disorder, consequence of alterations in gene and protein expression since the neurodevelopment that together to environmental factors will trigger the establishment of the disease. In the post-genomic era, proteomics has emerged as a promising strategy for revealing disease and treatment biomarkers as well as a tool for the comprehension of the mechanisms of schizophrenia pathobiology. Here, there is a discussion of the potential pathways and structures that are compromised in schizophrenia according to proteomic findings while studying five distinct brain regions of post-mortem tissue from schizophrenia patients and controls. Proteins involved in energy metabolism, calcium homeostasis, myelinization, and cytoskeleton have been recurrently found to be differentially expressed in schizophrenia brains. These findings may encourage new studies on the understanding of schizophrenia biochemical pathways and even new potential drug targets.
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spelling pubmed-35691162013-02-21 Proteomics as a Tool for Understanding Schizophrenia Martins-de-Souza, Daniel Clin Psychopharmacol Neurosci Review Schizophrenia is likely to be a multifactorial disorder, consequence of alterations in gene and protein expression since the neurodevelopment that together to environmental factors will trigger the establishment of the disease. In the post-genomic era, proteomics has emerged as a promising strategy for revealing disease and treatment biomarkers as well as a tool for the comprehension of the mechanisms of schizophrenia pathobiology. Here, there is a discussion of the potential pathways and structures that are compromised in schizophrenia according to proteomic findings while studying five distinct brain regions of post-mortem tissue from schizophrenia patients and controls. Proteins involved in energy metabolism, calcium homeostasis, myelinization, and cytoskeleton have been recurrently found to be differentially expressed in schizophrenia brains. These findings may encourage new studies on the understanding of schizophrenia biochemical pathways and even new potential drug targets. Korean College of Neuropsychopharmacology 2011-12 2011-12-31 /pmc/articles/PMC3569116/ /pubmed/23430140 http://dx.doi.org/10.9758/cpn.2011.9.3.95 Text en Copyright© 2011, Korean College of Neuropsychopharmacology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Martins-de-Souza, Daniel
Proteomics as a Tool for Understanding Schizophrenia
title Proteomics as a Tool for Understanding Schizophrenia
title_full Proteomics as a Tool for Understanding Schizophrenia
title_fullStr Proteomics as a Tool for Understanding Schizophrenia
title_full_unstemmed Proteomics as a Tool for Understanding Schizophrenia
title_short Proteomics as a Tool for Understanding Schizophrenia
title_sort proteomics as a tool for understanding schizophrenia
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569116/
https://www.ncbi.nlm.nih.gov/pubmed/23430140
http://dx.doi.org/10.9758/cpn.2011.9.3.95
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