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Evaluation of long-term consumption of omeprazole disadvantages: a network analysis
AIM: Evaluation of deregulated genes after long-term consuming of omeprazole via network analysis. BACKGROUND: Proton pump inhibitors (PPIs) are used to inhibit gastric high rate of acid secretion in patients. Omeprazole as a PPI is a common drug in this regard. Evaluation of long-term consumption o...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shaheed Beheshti University of Medical Sciences
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7881401/ https://www.ncbi.nlm.nih.gov/pubmed/33585010 |
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author | Nikzamir, Abdolrahim Rezaei-Tavirani, Mostafa Razzaghi, Mohhamadreza Rezaei Tavirani, Sina Hamzeloo-Moghadam, Maryam Esmaeili, Somayeh Hatami, Behzad Ahmadzadeh, Alireza |
author_facet | Nikzamir, Abdolrahim Rezaei-Tavirani, Mostafa Razzaghi, Mohhamadreza Rezaei Tavirani, Sina Hamzeloo-Moghadam, Maryam Esmaeili, Somayeh Hatami, Behzad Ahmadzadeh, Alireza |
author_sort | Nikzamir, Abdolrahim |
collection | PubMed |
description | AIM: Evaluation of deregulated genes after long-term consuming of omeprazole via network analysis. BACKGROUND: Proton pump inhibitors (PPIs) are used to inhibit gastric high rate of acid secretion in patients. Omeprazole as a PPI is a common drug in this regard. Evaluation of long-term consumption of omeprazole is studied in the present study via its effects on the gene expression of “human coronary artery endothelial cells”. METHODS: Net effect of the presence of omeprazole on gene expression profiles of “human coronary artery endothelial cells” was evaluated through data from gene expression omnibus (GEO). Results of protein-protein interaction (PPI) network analysis were assessed via biological process examination to find the critical deregulated genes after long-term consumption of omeprazole. RESULTS: “Negative regulation of muscle cell apoptotic process”, “negative regulation of DNA binding”, “telencephalon cell migration”, “forebrain cell migration” “response to cadmium ion”, “cell-cell recognition”, “positive regulation of protein targeting to mitochondrion”, and “central nervous system neuron development” were the clusters of biological processes that were associated to the long -term presence of omeprazole. The final critical deregulated genes were JAK2, PTK2, and NRG1. CONCLUSION: It can be concluded that cell cycle, proliferation, and apoptosis and several essential biological processes are affected and nervous system is a possible target related to the long-term consumption of omeprazole. |
format | Online Article Text |
id | pubmed-7881401 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Shaheed Beheshti University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-78814012021-02-13 Evaluation of long-term consumption of omeprazole disadvantages: a network analysis Nikzamir, Abdolrahim Rezaei-Tavirani, Mostafa Razzaghi, Mohhamadreza Rezaei Tavirani, Sina Hamzeloo-Moghadam, Maryam Esmaeili, Somayeh Hatami, Behzad Ahmadzadeh, Alireza Gastroenterol Hepatol Bed Bench Original Article AIM: Evaluation of deregulated genes after long-term consuming of omeprazole via network analysis. BACKGROUND: Proton pump inhibitors (PPIs) are used to inhibit gastric high rate of acid secretion in patients. Omeprazole as a PPI is a common drug in this regard. Evaluation of long-term consumption of omeprazole is studied in the present study via its effects on the gene expression of “human coronary artery endothelial cells”. METHODS: Net effect of the presence of omeprazole on gene expression profiles of “human coronary artery endothelial cells” was evaluated through data from gene expression omnibus (GEO). Results of protein-protein interaction (PPI) network analysis were assessed via biological process examination to find the critical deregulated genes after long-term consumption of omeprazole. RESULTS: “Negative regulation of muscle cell apoptotic process”, “negative regulation of DNA binding”, “telencephalon cell migration”, “forebrain cell migration” “response to cadmium ion”, “cell-cell recognition”, “positive regulation of protein targeting to mitochondrion”, and “central nervous system neuron development” were the clusters of biological processes that were associated to the long -term presence of omeprazole. The final critical deregulated genes were JAK2, PTK2, and NRG1. CONCLUSION: It can be concluded that cell cycle, proliferation, and apoptosis and several essential biological processes are affected and nervous system is a possible target related to the long-term consumption of omeprazole. Shaheed Beheshti University of Medical Sciences 2020 /pmc/articles/PMC7881401/ /pubmed/33585010 Text en ©2020 RIGLD, Research Institute for Gastroenterology and Liver Diseases This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Nikzamir, Abdolrahim Rezaei-Tavirani, Mostafa Razzaghi, Mohhamadreza Rezaei Tavirani, Sina Hamzeloo-Moghadam, Maryam Esmaeili, Somayeh Hatami, Behzad Ahmadzadeh, Alireza Evaluation of long-term consumption of omeprazole disadvantages: a network analysis |
title | Evaluation of long-term consumption of omeprazole disadvantages: a network analysis |
title_full | Evaluation of long-term consumption of omeprazole disadvantages: a network analysis |
title_fullStr | Evaluation of long-term consumption of omeprazole disadvantages: a network analysis |
title_full_unstemmed | Evaluation of long-term consumption of omeprazole disadvantages: a network analysis |
title_short | Evaluation of long-term consumption of omeprazole disadvantages: a network analysis |
title_sort | evaluation of long-term consumption of omeprazole disadvantages: a network analysis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7881401/ https://www.ncbi.nlm.nih.gov/pubmed/33585010 |
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