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Systematic review of overlapping microRNA patterns in COVID-19 and idiopathic pulmonary fibrosis

BACKGROUND: Pulmonary fibrosis is an emerging complication of SARS-CoV-2 infection. In this study, we speculate that patients with COVID-19 and idiopathic pulmonary fibrosis (IPF) may share aberrant expressed microRNAs (miRNAs) associated to the progression of lung fibrosis. OBJECTIVE: To identify m...

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Autores principales: Guiot, Julien, Henket, Monique, Remacle, Claire, Cambier, Maureen, Struman, Ingrid, Winandy, Marie, Moermans, Catherine, Louis, Edouard, Malaise, Michel, Ribbens, Clio, Louis, Renaud, Njock, Makon-Sébastien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10105547/
https://www.ncbi.nlm.nih.gov/pubmed/37061683
http://dx.doi.org/10.1186/s12931-023-02413-6
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author Guiot, Julien
Henket, Monique
Remacle, Claire
Cambier, Maureen
Struman, Ingrid
Winandy, Marie
Moermans, Catherine
Louis, Edouard
Malaise, Michel
Ribbens, Clio
Louis, Renaud
Njock, Makon-Sébastien
author_facet Guiot, Julien
Henket, Monique
Remacle, Claire
Cambier, Maureen
Struman, Ingrid
Winandy, Marie
Moermans, Catherine
Louis, Edouard
Malaise, Michel
Ribbens, Clio
Louis, Renaud
Njock, Makon-Sébastien
author_sort Guiot, Julien
collection PubMed
description BACKGROUND: Pulmonary fibrosis is an emerging complication of SARS-CoV-2 infection. In this study, we speculate that patients with COVID-19 and idiopathic pulmonary fibrosis (IPF) may share aberrant expressed microRNAs (miRNAs) associated to the progression of lung fibrosis. OBJECTIVE: To identify miRNAs presenting similar alteration in COVID-19 and IPF, and describe their impact on fibrogenesis. METHODS: A systematic review of the literature published between 2010 and January 2022 (PROSPERO, CRD42022341016) was conducted using the key words (COVID-19 OR SARS-CoV-2) AND (microRNA OR miRNA) or (idiopathic pulmonary fibrosis OR IPF) AND (microRNA OR miRNA) in Title/Abstract. RESULTS: Of the 1988 references considered, 70 original articles were appropriate for data extraction: 27 studies focused on miRNAs in COVID-19, and 43 on miRNAs in IPF. 34 miRNAs were overlapping in COVID-19 and IPF, 7 miRNAs presenting an upregulation (miR-19a-3p, miR-200c-3p, miR-21-5p, miR-145-5p, miR-199a-5p, miR-23b and miR-424) and 9 miRNAs a downregulation (miR-17-5p, miR-20a-5p, miR-92a-3p, miR-141-3p, miR-16-5p, miR-142-5p, miR-486-5p, miR-708-3p and miR-150-5p). CONCLUSION: Several studies reported elevated levels of profibrotic miRNAs in COVID-19 context. In addition, the balance of antifibrotic miRNAs responsible of the modulation of fibrotic processes is impaired in COVID-19. This evidence suggests that the deregulation of fibrotic-related miRNAs participates in the development of fibrotic lesions in the lung of post-COVID-19 patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12931-023-02413-6.
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spelling pubmed-101055472023-04-17 Systematic review of overlapping microRNA patterns in COVID-19 and idiopathic pulmonary fibrosis Guiot, Julien Henket, Monique Remacle, Claire Cambier, Maureen Struman, Ingrid Winandy, Marie Moermans, Catherine Louis, Edouard Malaise, Michel Ribbens, Clio Louis, Renaud Njock, Makon-Sébastien Respir Res Review BACKGROUND: Pulmonary fibrosis is an emerging complication of SARS-CoV-2 infection. In this study, we speculate that patients with COVID-19 and idiopathic pulmonary fibrosis (IPF) may share aberrant expressed microRNAs (miRNAs) associated to the progression of lung fibrosis. OBJECTIVE: To identify miRNAs presenting similar alteration in COVID-19 and IPF, and describe their impact on fibrogenesis. METHODS: A systematic review of the literature published between 2010 and January 2022 (PROSPERO, CRD42022341016) was conducted using the key words (COVID-19 OR SARS-CoV-2) AND (microRNA OR miRNA) or (idiopathic pulmonary fibrosis OR IPF) AND (microRNA OR miRNA) in Title/Abstract. RESULTS: Of the 1988 references considered, 70 original articles were appropriate for data extraction: 27 studies focused on miRNAs in COVID-19, and 43 on miRNAs in IPF. 34 miRNAs were overlapping in COVID-19 and IPF, 7 miRNAs presenting an upregulation (miR-19a-3p, miR-200c-3p, miR-21-5p, miR-145-5p, miR-199a-5p, miR-23b and miR-424) and 9 miRNAs a downregulation (miR-17-5p, miR-20a-5p, miR-92a-3p, miR-141-3p, miR-16-5p, miR-142-5p, miR-486-5p, miR-708-3p and miR-150-5p). CONCLUSION: Several studies reported elevated levels of profibrotic miRNAs in COVID-19 context. In addition, the balance of antifibrotic miRNAs responsible of the modulation of fibrotic processes is impaired in COVID-19. This evidence suggests that the deregulation of fibrotic-related miRNAs participates in the development of fibrotic lesions in the lung of post-COVID-19 patients. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12931-023-02413-6. BioMed Central 2023-04-15 2023 /pmc/articles/PMC10105547/ /pubmed/37061683 http://dx.doi.org/10.1186/s12931-023-02413-6 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Guiot, Julien
Henket, Monique
Remacle, Claire
Cambier, Maureen
Struman, Ingrid
Winandy, Marie
Moermans, Catherine
Louis, Edouard
Malaise, Michel
Ribbens, Clio
Louis, Renaud
Njock, Makon-Sébastien
Systematic review of overlapping microRNA patterns in COVID-19 and idiopathic pulmonary fibrosis
title Systematic review of overlapping microRNA patterns in COVID-19 and idiopathic pulmonary fibrosis
title_full Systematic review of overlapping microRNA patterns in COVID-19 and idiopathic pulmonary fibrosis
title_fullStr Systematic review of overlapping microRNA patterns in COVID-19 and idiopathic pulmonary fibrosis
title_full_unstemmed Systematic review of overlapping microRNA patterns in COVID-19 and idiopathic pulmonary fibrosis
title_short Systematic review of overlapping microRNA patterns in COVID-19 and idiopathic pulmonary fibrosis
title_sort systematic review of overlapping microrna patterns in covid-19 and idiopathic pulmonary fibrosis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10105547/
https://www.ncbi.nlm.nih.gov/pubmed/37061683
http://dx.doi.org/10.1186/s12931-023-02413-6
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