Circulating microRNAs Suggest Networks Associated with Biological Functions in Aggressive Refractory Type 2 Celiac Disease
Despite following a gluten-free diet, which is currently the only effective therapy for celiac disease, about 5% of patients can develop serious complications, which in the case of refractory type 2 could evolve towards intestinal lymphoma. In this study, we have identified a set of 15 microRNAs in...
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| Published in: | Biomedicines Vol. 10; no. 6; p. 1408 |
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| Main Authors: | , , , , , , , , , , , , , , |
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| Language: | English |
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| Abstract | Despite following a gluten-free diet, which is currently the only effective therapy for celiac disease, about 5% of patients can develop serious complications, which in the case of refractory type 2 could evolve towards intestinal lymphoma. In this study, we have identified a set of 15 microRNAs in serum discriminating between the two types of refractory disease. Upregulated miR-770-5p, miR-181b-2-3p, miR-1193, and miR-1226-3p could be useful for the better stratification of patients and the monitoring of disease development, while miR-490-3p was found to be dysregulated in patients with refractory type 1. Finally, by using bioinformatic tools applied to the analysis of the targets of dysregulated microRNAs, we have completed a more precise assessment of their functions. These mainly include the pathway of response to Transforming Growth Factor β cell–cell signaling by Wnt; epigenetic regulation, especially novel networks associated with transcriptional and post-transcriptional alterations; and the well-known inflammatory profiles. |
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| AbstractList | Despite following a gluten-free diet, which is currently the only effective therapy for celiac disease, about 5% of patients can develop serious complications, which in the case of refractory type 2 could evolve towards intestinal lymphoma. In this study, we have identified a set of 15 microRNAs in serum discriminating between the two types of refractory disease. Upregulated miR-770-5p, miR-181b-2-3p, miR-1193, and miR-1226-3p could be useful for the better stratification of patients and the monitoring of disease development, while miR-490-3p was found to be dysregulated in patients with refractory type 1. Finally, by using bioinformatic tools applied to the analysis of the targets of dysregulated microRNAs, we have completed a more precise assessment of their functions. These mainly include the pathway of response to Transforming Growth Factor β cell–cell signaling by Wnt; epigenetic regulation, especially novel networks associated with transcriptional and post-transcriptional alterations; and the well-known inflammatory profiles. Despite following a gluten-free diet, which is currently the only effective therapy for celiac disease, about 5% of patients can develop serious complications, which in the case of refractory type 2 could evolve towards intestinal lymphoma. In this study, we have identified a set of 15 microRNAs in serum discriminating between the two types of refractory disease. Upregulated miR-770-5p, miR-181b-2-3p, miR-1193, and miR-1226-3p could be useful for the better stratification of patients and the monitoring of disease development, while miR-490-3p was found to be dysregulated in patients with refractory type 1. Finally, by using bioinformatic tools applied to the analysis of the targets of dysregulated microRNAs, we have completed a more precise assessment of their functions. These mainly include the pathway of response to Transforming Growth Factor β cell-cell signaling by Wnt; epigenetic regulation, especially novel networks associated with transcriptional and post-transcriptional alterations; and the well-known inflammatory profiles.Despite following a gluten-free diet, which is currently the only effective therapy for celiac disease, about 5% of patients can develop serious complications, which in the case of refractory type 2 could evolve towards intestinal lymphoma. In this study, we have identified a set of 15 microRNAs in serum discriminating between the two types of refractory disease. Upregulated miR-770-5p, miR-181b-2-3p, miR-1193, and miR-1226-3p could be useful for the better stratification of patients and the monitoring of disease development, while miR-490-3p was found to be dysregulated in patients with refractory type 1. Finally, by using bioinformatic tools applied to the analysis of the targets of dysregulated microRNAs, we have completed a more precise assessment of their functions. These mainly include the pathway of response to Transforming Growth Factor β cell-cell signaling by Wnt; epigenetic regulation, especially novel networks associated with transcriptional and post-transcriptional alterations; and the well-known inflammatory profiles. |
| Audience | Academic |
| Author | Taccioli, Cristian Bianchi, Nicoletta Bergamini, Carlo Doneda, Luisa Elli, Luca Scaramella, Lucia Vecchi, Maurizio Roncoroni, Leda Colapietro, Patrizia Lombardo, Vincenza Scricciolo, Alice Vaira, Valentina Terrazzan, Anna Nandi, Nicoletta Terranova, Leonardo |
| AuthorAffiliation | 1 Department of Translational Medicine, University of Ferrara, Street L. Borsari 46, 44121 Ferrara, Italy; nicoletta.bianchi@unife.it (N.B.); anna.terrazzan@unife.it (A.T.) 2 Department of Biomedical, Surgical and Dental Sciences, University of Milan, Street Pascal 36, 20133 Milan, Italy; luisa.doneda@unimi.it (L.D.); leda.roncoroni@unimi.it (L.R.) 5 Division of Pathology, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, Street F. Sforza 35, 20122 Milan, Italy; valentina.vaira@unimi.it 3 Center for Prevention and Diagnosis of Celiac Disease, Gastroenterology and Endoscopy Unit, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, 20122 Milan, Italy; alice.scricciolo@policlinico.mi.it (A.S.); vincenza.lombardo@policlinico.mi.it (V.L.); maurizio.vecchi@unimi.it (M.V.); lucia.scaramella@policlinico.mi.it (L.S.); nicoletta.nandi@unimi.it (N.N.) 4 Department of Animal Medicine, Production and Health, University of Padova, 35020 Legnaro, Italy; cristian.taccioli@unipd.it 6 Depar |
| AuthorAffiliation_xml | – name: 2 Department of Biomedical, Surgical and Dental Sciences, University of Milan, Street Pascal 36, 20133 Milan, Italy; luisa.doneda@unimi.it (L.D.); leda.roncoroni@unimi.it (L.R.) – name: 1 Department of Translational Medicine, University of Ferrara, Street L. Borsari 46, 44121 Ferrara, Italy; nicoletta.bianchi@unife.it (N.B.); anna.terrazzan@unife.it (A.T.) – name: 7 Respiratory Unit and Cystic Fibrosis Adult Center, Internal Medicine Department, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, Street F. Sforza 35, 20122 Milan, Italy; leonardo.terranova@policlinico.mi.it – name: 6 Department of Pathophysiology and Transplantation, University of Milan, Street F. Sforza 35, 20122 Milan, Italy; patrizia.colapietro@unimi.it – name: 8 Department of Neuroscience and Rehabilitation, University of Ferrara, Street L. Borsari 46, 44121 Ferrara, Italy; carlo.bergamini@unife.it – name: 4 Department of Animal Medicine, Production and Health, University of Padova, 35020 Legnaro, Italy; cristian.taccioli@unipd.it – name: 5 Division of Pathology, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, Street F. Sforza 35, 20122 Milan, Italy; valentina.vaira@unimi.it – name: 3 Center for Prevention and Diagnosis of Celiac Disease, Gastroenterology and Endoscopy Unit, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, 20122 Milan, Italy; alice.scricciolo@policlinico.mi.it (A.S.); vincenza.lombardo@policlinico.mi.it (V.L.); maurizio.vecchi@unimi.it (M.V.); lucia.scaramella@policlinico.mi.it (L.S.); nicoletta.nandi@unimi.it (N.N.) |
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