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Protein-Protein Interaction Network Analysis Revealed a New Prospective of Posttraumatic Stress Disorder
BACKGROUND: Posttraumatic stress disorder (PTSD) is known by a number of mental disorders, including recurring memories of trauma, mental appalling, and escaping of sign that make them recall the trauma in question. Clinical interviews serve as the main diagnostic tool for PTSD. With respect to trea...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Salvia Medical Sciences Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8344167/ https://www.ncbi.nlm.nih.gov/pubmed/34466439 http://dx.doi.org/10.22086/gmj.v0i0.1137 |
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author | Okhovatian, Farshad Rezaei Tavirani, Mostafa Rostami-Nejad, Mohammad Rezaei Tavirani, Sina |
author_facet | Okhovatian, Farshad Rezaei Tavirani, Mostafa Rostami-Nejad, Mohammad Rezaei Tavirani, Sina |
author_sort | Okhovatian, Farshad |
collection | PubMed |
description | BACKGROUND: Posttraumatic stress disorder (PTSD) is known by a number of mental disorders, including recurring memories of trauma, mental appalling, and escaping of sign that make them recall the trauma in question. Clinical interviews serve as the main diagnostic tool for PTSD. With respect to treatment, either pharmacotherapy or psychotherapy or a combination of both is used as a therapeutic method for PTSD. In this study, a number of crucial genes related to PTSD, which can be considered as biomarker candidates, were represented. MATERIALS AND METHODS: The genes related to PTSD were extracted from the STRING database and organized in a protein-protein interaction network with the help of Cytoscape software version 3.6.0. The network was analyzed, and the important genes were introduced based on central indices. The biological processes related to the crucial genes were enriched via gene ontology using ClueGO. RESULTS: From a total of 100 genes, 63 genes were extracted that formed the main connected component, and of these, 12 crucial genes-POMC, BDNF, FOS, NR3C1, CRH, IL6, NPS, HTR1A, NPY, CREB1, CRHR1, and TAC1-were introduced. Biological processes were classified into the regulation of corticosterone, regulation of behavior, response to fungus, multicellular organism response to stress, and associative learning CONCLUSION: The introduced 12 crucial genes can be used as a biomarker panel related to PTSD and can be considered as a diagnostic reagent or drug target; however, more investigations are needed to use these genes as biomarkers. |
format | Online Article Text |
id | pubmed-8344167 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Salvia Medical Sciences Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-83441672021-08-30 Protein-Protein Interaction Network Analysis Revealed a New Prospective of Posttraumatic Stress Disorder Okhovatian, Farshad Rezaei Tavirani, Mostafa Rostami-Nejad, Mohammad Rezaei Tavirani, Sina Galen Med J Original Article BACKGROUND: Posttraumatic stress disorder (PTSD) is known by a number of mental disorders, including recurring memories of trauma, mental appalling, and escaping of sign that make them recall the trauma in question. Clinical interviews serve as the main diagnostic tool for PTSD. With respect to treatment, either pharmacotherapy or psychotherapy or a combination of both is used as a therapeutic method for PTSD. In this study, a number of crucial genes related to PTSD, which can be considered as biomarker candidates, were represented. MATERIALS AND METHODS: The genes related to PTSD were extracted from the STRING database and organized in a protein-protein interaction network with the help of Cytoscape software version 3.6.0. The network was analyzed, and the important genes were introduced based on central indices. The biological processes related to the crucial genes were enriched via gene ontology using ClueGO. RESULTS: From a total of 100 genes, 63 genes were extracted that formed the main connected component, and of these, 12 crucial genes-POMC, BDNF, FOS, NR3C1, CRH, IL6, NPS, HTR1A, NPY, CREB1, CRHR1, and TAC1-were introduced. Biological processes were classified into the regulation of corticosterone, regulation of behavior, response to fungus, multicellular organism response to stress, and associative learning CONCLUSION: The introduced 12 crucial genes can be used as a biomarker panel related to PTSD and can be considered as a diagnostic reagent or drug target; however, more investigations are needed to use these genes as biomarkers. Salvia Medical Sciences Ltd 2018-05-29 /pmc/articles/PMC8344167/ /pubmed/34466439 http://dx.doi.org/10.22086/gmj.v0i0.1137 Text en Copyright© 2018, Galen Medical Journal. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ) |
spellingShingle | Original Article Okhovatian, Farshad Rezaei Tavirani, Mostafa Rostami-Nejad, Mohammad Rezaei Tavirani, Sina Protein-Protein Interaction Network Analysis Revealed a New Prospective of Posttraumatic Stress Disorder |
title | Protein-Protein Interaction Network Analysis Revealed a New Prospective of Posttraumatic Stress Disorder |
title_full | Protein-Protein Interaction Network Analysis Revealed a New Prospective of Posttraumatic Stress Disorder |
title_fullStr | Protein-Protein Interaction Network Analysis Revealed a New Prospective of Posttraumatic Stress Disorder |
title_full_unstemmed | Protein-Protein Interaction Network Analysis Revealed a New Prospective of Posttraumatic Stress Disorder |
title_short | Protein-Protein Interaction Network Analysis Revealed a New Prospective of Posttraumatic Stress Disorder |
title_sort | protein-protein interaction network analysis revealed a new prospective of posttraumatic stress disorder |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8344167/ https://www.ncbi.nlm.nih.gov/pubmed/34466439 http://dx.doi.org/10.22086/gmj.v0i0.1137 |
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