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Expression analysis of protein inhibitor of activated STAT (PIAS) genes in IFNβ-treated multiple sclerosis patients
OBJECTIVES: Protein inhibitors of activated STAT (PIAS) are transcription co-regulator of the Janus kinase/signal transducer and activator of transcription signaling pathway as well as nuclear factor-κB family of transcription factors. Both of them are involved in cytokine release during inflammator...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6289119/ https://www.ncbi.nlm.nih.gov/pubmed/30584347 http://dx.doi.org/10.2147/JIR.S187414 |
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author | Taheri, Mohammad Azimi, Ghazaleh Sayad, Arezou Mazdeh, Mehrdokht Arsang-Jang, Shahram Omrani, Mir Davood Ghafori-Fard, Soudeh |
author_facet | Taheri, Mohammad Azimi, Ghazaleh Sayad, Arezou Mazdeh, Mehrdokht Arsang-Jang, Shahram Omrani, Mir Davood Ghafori-Fard, Soudeh |
author_sort | Taheri, Mohammad |
collection | PubMed |
description | OBJECTIVES: Protein inhibitors of activated STAT (PIAS) are transcription co-regulator of the Janus kinase/signal transducer and activator of transcription signaling pathway as well as nuclear factor-κB family of transcription factors. Both of them are involved in cytokine release during inflammatory response. PATIENTS AND METHODS: Considering the role of cytokine imbalance in the pathogenesis of multiple sclerosis (MS), we compared blood expressions of PIAS1-4 genes in 48 interferon β (IFNβ)-treated MS patients with those of healthy subjects by means of real time PCR. RESULTS: Although the expression levels of these genes were not significantly different between MS patients and healthy subjects, significant inverse correlations have been found between PIAS1 expression and age at disease onset. PIAS2 and PIAS3 expressions were inversely correlated with Expanded Disability Status Scale (EDSS) in patients. Moreover, PIAS3 expression was correlated with disease duration in patients and with age in controls. In addition, PIAS4 expression was inversely correlated with EDSS and age at disease onset while it was positively correlated with disease duration. CONCLUSION: The present study provides evidences for altered expression of PIAS genes in IFNβ-treated MS patients compared with healthy subjects. However, future studies are needed for elaboration of their exact function in this disorder. |
format | Online Article Text |
id | pubmed-6289119 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62891192018-12-24 Expression analysis of protein inhibitor of activated STAT (PIAS) genes in IFNβ-treated multiple sclerosis patients Taheri, Mohammad Azimi, Ghazaleh Sayad, Arezou Mazdeh, Mehrdokht Arsang-Jang, Shahram Omrani, Mir Davood Ghafori-Fard, Soudeh J Inflamm Res Original Research OBJECTIVES: Protein inhibitors of activated STAT (PIAS) are transcription co-regulator of the Janus kinase/signal transducer and activator of transcription signaling pathway as well as nuclear factor-κB family of transcription factors. Both of them are involved in cytokine release during inflammatory response. PATIENTS AND METHODS: Considering the role of cytokine imbalance in the pathogenesis of multiple sclerosis (MS), we compared blood expressions of PIAS1-4 genes in 48 interferon β (IFNβ)-treated MS patients with those of healthy subjects by means of real time PCR. RESULTS: Although the expression levels of these genes were not significantly different between MS patients and healthy subjects, significant inverse correlations have been found between PIAS1 expression and age at disease onset. PIAS2 and PIAS3 expressions were inversely correlated with Expanded Disability Status Scale (EDSS) in patients. Moreover, PIAS3 expression was correlated with disease duration in patients and with age in controls. In addition, PIAS4 expression was inversely correlated with EDSS and age at disease onset while it was positively correlated with disease duration. CONCLUSION: The present study provides evidences for altered expression of PIAS genes in IFNβ-treated MS patients compared with healthy subjects. However, future studies are needed for elaboration of their exact function in this disorder. Dove Medical Press 2018-12-06 /pmc/articles/PMC6289119/ /pubmed/30584347 http://dx.doi.org/10.2147/JIR.S187414 Text en © 2018 Taheri et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Taheri, Mohammad Azimi, Ghazaleh Sayad, Arezou Mazdeh, Mehrdokht Arsang-Jang, Shahram Omrani, Mir Davood Ghafori-Fard, Soudeh Expression analysis of protein inhibitor of activated STAT (PIAS) genes in IFNβ-treated multiple sclerosis patients |
title | Expression analysis of protein inhibitor of activated STAT (PIAS) genes in IFNβ-treated multiple sclerosis patients |
title_full | Expression analysis of protein inhibitor of activated STAT (PIAS) genes in IFNβ-treated multiple sclerosis patients |
title_fullStr | Expression analysis of protein inhibitor of activated STAT (PIAS) genes in IFNβ-treated multiple sclerosis patients |
title_full_unstemmed | Expression analysis of protein inhibitor of activated STAT (PIAS) genes in IFNβ-treated multiple sclerosis patients |
title_short | Expression analysis of protein inhibitor of activated STAT (PIAS) genes in IFNβ-treated multiple sclerosis patients |
title_sort | expression analysis of protein inhibitor of activated stat (pias) genes in ifnβ-treated multiple sclerosis patients |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6289119/ https://www.ncbi.nlm.nih.gov/pubmed/30584347 http://dx.doi.org/10.2147/JIR.S187414 |
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