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MicroRNAs overexpressed in Crohn’s disease and their interactions with mechanisms of epigenetic regulation explain novel aspects of Crohn’s disease pathogenesis

BACKGROUND: In this review, we were interested to identify the wide universe of enzymes associated with epigenetic modifications, whose gene expression is regulated by miRNAs with a high relative abundance in Crohn's disease (CD) affected tissues, with the aim to determine their impact in the p...

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Autores principales: Fernández-Ponce, Cecilia, Navarro Quiroz, Roberto, Díaz Perez, Anderson, Aroca Martinez, Gustavo, Cadena Bonfanti, Andrés, Acosta Hoyos, Antonio, Gómez Escorcia, Lorena, Hernández Agudelo, Sandra, Orozco Sánchez, Christian, Villarreal Camacho, José, Atencio Ibarra, Linda, Consuegra Machado, Jose, Espinoza Garavito, Alberto, García-Cózar, Francisco, Navarro Quiroz, Elkin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7890887/
https://www.ncbi.nlm.nih.gov/pubmed/33602320
http://dx.doi.org/10.1186/s13148-021-01022-8
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author Fernández-Ponce, Cecilia
Navarro Quiroz, Roberto
Díaz Perez, Anderson
Aroca Martinez, Gustavo
Cadena Bonfanti, Andrés
Acosta Hoyos, Antonio
Gómez Escorcia, Lorena
Hernández Agudelo, Sandra
Orozco Sánchez, Christian
Villarreal Camacho, José
Atencio Ibarra, Linda
Consuegra Machado, Jose
Espinoza Garavito, Alberto
García-Cózar, Francisco
Navarro Quiroz, Elkin
author_facet Fernández-Ponce, Cecilia
Navarro Quiroz, Roberto
Díaz Perez, Anderson
Aroca Martinez, Gustavo
Cadena Bonfanti, Andrés
Acosta Hoyos, Antonio
Gómez Escorcia, Lorena
Hernández Agudelo, Sandra
Orozco Sánchez, Christian
Villarreal Camacho, José
Atencio Ibarra, Linda
Consuegra Machado, Jose
Espinoza Garavito, Alberto
García-Cózar, Francisco
Navarro Quiroz, Elkin
author_sort Fernández-Ponce, Cecilia
collection PubMed
description BACKGROUND: In this review, we were interested to identify the wide universe of enzymes associated with epigenetic modifications, whose gene expression is regulated by miRNAs with a high relative abundance in Crohn's disease (CD) affected tissues, with the aim to determine their impact in the pathogenesis and evolution of the disease. METHODS: We used HMDD and Bibliometrix R-package in order to identify the miRNAs overexpressed in CD. The identified enzymes associated with epigenetic mechanisms and post-translational modifications, regulated by miRNAs upregulated in CD, were analyzed using String v11 database. RESULTS: We found 190 miRNAs with great abundance in patients with CD, of which 26 miRNAs regulate the gene expression of enzymes known to catalyze epigenetic modifications involved in essentials pathophysiological processes, such as chromatin architecture reorganization, immune response regulation including CD4+ T cells polarization, integrity of gut mucosa, gut microbiota composition and tumorigenesis. CONCLUSION: The integrated analysis of miRNAs with a high relative abundance in patients with CD showed a combined and superimposed gene expression regulation of enzymes associated with relevant epigenetic mechanisms and that could explain, in part, the pathogenesis of CD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13148-021-01022-8.
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spelling pubmed-78908872021-02-22 MicroRNAs overexpressed in Crohn’s disease and their interactions with mechanisms of epigenetic regulation explain novel aspects of Crohn’s disease pathogenesis Fernández-Ponce, Cecilia Navarro Quiroz, Roberto Díaz Perez, Anderson Aroca Martinez, Gustavo Cadena Bonfanti, Andrés Acosta Hoyos, Antonio Gómez Escorcia, Lorena Hernández Agudelo, Sandra Orozco Sánchez, Christian Villarreal Camacho, José Atencio Ibarra, Linda Consuegra Machado, Jose Espinoza Garavito, Alberto García-Cózar, Francisco Navarro Quiroz, Elkin Clin Epigenetics Review BACKGROUND: In this review, we were interested to identify the wide universe of enzymes associated with epigenetic modifications, whose gene expression is regulated by miRNAs with a high relative abundance in Crohn's disease (CD) affected tissues, with the aim to determine their impact in the pathogenesis and evolution of the disease. METHODS: We used HMDD and Bibliometrix R-package in order to identify the miRNAs overexpressed in CD. The identified enzymes associated with epigenetic mechanisms and post-translational modifications, regulated by miRNAs upregulated in CD, were analyzed using String v11 database. RESULTS: We found 190 miRNAs with great abundance in patients with CD, of which 26 miRNAs regulate the gene expression of enzymes known to catalyze epigenetic modifications involved in essentials pathophysiological processes, such as chromatin architecture reorganization, immune response regulation including CD4+ T cells polarization, integrity of gut mucosa, gut microbiota composition and tumorigenesis. CONCLUSION: The integrated analysis of miRNAs with a high relative abundance in patients with CD showed a combined and superimposed gene expression regulation of enzymes associated with relevant epigenetic mechanisms and that could explain, in part, the pathogenesis of CD. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13148-021-01022-8. BioMed Central 2021-02-18 /pmc/articles/PMC7890887/ /pubmed/33602320 http://dx.doi.org/10.1186/s13148-021-01022-8 Text en © The Author(s) 2021 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/. The Creative Commons Public Domain Dedication waiver (http://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
Fernández-Ponce, Cecilia
Navarro Quiroz, Roberto
Díaz Perez, Anderson
Aroca Martinez, Gustavo
Cadena Bonfanti, Andrés
Acosta Hoyos, Antonio
Gómez Escorcia, Lorena
Hernández Agudelo, Sandra
Orozco Sánchez, Christian
Villarreal Camacho, José
Atencio Ibarra, Linda
Consuegra Machado, Jose
Espinoza Garavito, Alberto
García-Cózar, Francisco
Navarro Quiroz, Elkin
MicroRNAs overexpressed in Crohn’s disease and their interactions with mechanisms of epigenetic regulation explain novel aspects of Crohn’s disease pathogenesis
title MicroRNAs overexpressed in Crohn’s disease and their interactions with mechanisms of epigenetic regulation explain novel aspects of Crohn’s disease pathogenesis
title_full MicroRNAs overexpressed in Crohn’s disease and their interactions with mechanisms of epigenetic regulation explain novel aspects of Crohn’s disease pathogenesis
title_fullStr MicroRNAs overexpressed in Crohn’s disease and their interactions with mechanisms of epigenetic regulation explain novel aspects of Crohn’s disease pathogenesis
title_full_unstemmed MicroRNAs overexpressed in Crohn’s disease and their interactions with mechanisms of epigenetic regulation explain novel aspects of Crohn’s disease pathogenesis
title_short MicroRNAs overexpressed in Crohn’s disease and their interactions with mechanisms of epigenetic regulation explain novel aspects of Crohn’s disease pathogenesis
title_sort micrornas overexpressed in crohn’s disease and their interactions with mechanisms of epigenetic regulation explain novel aspects of crohn’s disease pathogenesis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7890887/
https://www.ncbi.nlm.nih.gov/pubmed/33602320
http://dx.doi.org/10.1186/s13148-021-01022-8
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