Colonic mucosal and serum expression of microRNAs in canine large intestinal inflammatory bowel disease

Background Canine inflammatory bowel disease (IBD) is a group of chronic gastrointestinal (GI) disorders of still largely unknown etiology. Canine IBD diagnosis is time-consuming and costly as other diseases with similar signs should be initially excluded. In human IBD microRNA (miR) expression chan...

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Veröffentlicht in:BMC veterinary research 2020-02, Vol.16 (1), p.69-69, Article 69
Hauptverfasser: Konstantinidis, Alexandros, Pardali, Dimitra, Adamama-Moraitou, Katerina K., Gazouli, Maria, Dovas, Chrysostomos I., Legaki, Evangelia, Brellou, Georgia D., Savvas, Ioannis, Jergens, Albert E., Rallis, Timoleon S., Allenspach, Karin
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container_title BMC veterinary research
container_volume 16
creator Konstantinidis, Alexandros
Pardali, Dimitra
Adamama-Moraitou, Katerina K.
Gazouli, Maria
Dovas, Chrysostomos I.
Legaki, Evangelia
Brellou, Georgia D.
Savvas, Ioannis
Jergens, Albert E.
Rallis, Timoleon S.
Allenspach, Karin
description Background Canine inflammatory bowel disease (IBD) is a group of chronic gastrointestinal (GI) disorders of still largely unknown etiology. Canine IBD diagnosis is time-consuming and costly as other diseases with similar signs should be initially excluded. In human IBD microRNA (miR) expression changes have been reported in GI mucosa and blood. Thus, there is a possibility that miRs may provide insight into disease pathogenesis, diagnosis and even treatment of canine IBD. The aim of this study was to determine the colonic mucosal and serum relative expression of a miRs panel in dogs with large intestinal IBD and healthy control dogs. Results Compared to healthy control dogs, dogs with large intestinal IBD showed significantly increased relative expression of miR-16, miR-21, miR-122 and miR-147 in the colonic mucosa and serum, while the relative expression of miR-185, miR-192 and miR-223 was significantly decreased. Relative expression of miR-146a was significantly increased only in the serum of dogs with large intestinal IBD. Furthermore, serum miR-192 and miR-223 relative expression correlated to disease activity and endoscopic score, respectively. Conclusion Our data suggest the existence of dysregulated miRs expression patterns in canine IBD and support the potential future use of serum miRs as useful noninvasive biomarkers.
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Canine IBD diagnosis is time-consuming and costly as other diseases with similar signs should be initially excluded. In human IBD microRNA (miR) expression changes have been reported in GI mucosa and blood. Thus, there is a possibility that miRs may provide insight into disease pathogenesis, diagnosis and even treatment of canine IBD. The aim of this study was to determine the colonic mucosal and serum relative expression of a miRs panel in dogs with large intestinal IBD and healthy control dogs. Results Compared to healthy control dogs, dogs with large intestinal IBD showed significantly increased relative expression of miR-16, miR-21, miR-122 and miR-147 in the colonic mucosa and serum, while the relative expression of miR-185, miR-192 and miR-223 was significantly decreased. Relative expression of miR-146a was significantly increased only in the serum of dogs with large intestinal IBD. Furthermore, serum miR-192 and miR-223 relative expression correlated to disease activity and endoscopic score, respectively. Conclusion Our data suggest the existence of dysregulated miRs expression patterns in canine IBD and support the potential future use of serum miRs as useful noninvasive biomarkers.</description><identifier>ISSN: 1746-6148</identifier><identifier>EISSN: 1746-6148</identifier><identifier>DOI: 10.1186/s12917-020-02287-6</identifier><identifier>PMID: 32087719</identifier><language>eng</language><publisher>LONDON: Springer Nature</publisher><subject>Apoptosis ; Binding sites ; Biomarker ; Biomarkers ; Colon ; Colonoscopy ; Dog ; Inflammation ; Inflammatory bowel disease ; Inflammatory bowel diseases ; Intestine ; Leukemia ; Life Sciences &amp; Biomedicine ; MicroRNAs ; miRNA ; Mucosa ; Pathogenesis ; Science &amp; Technology ; Studies ; Tumor necrosis factor-TNF ; Veterinary Sciences</subject><ispartof>BMC veterinary research, 2020-02, Vol.16 (1), p.69-69, Article 69</ispartof><rights>2020. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>15</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000517326500001</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c496t-f05d6f3c3fa4392b597844c845888b8459ccb3638fad21d17b7b3fc6b64d30d63</citedby><cites>FETCH-LOGICAL-c496t-f05d6f3c3fa4392b597844c845888b8459ccb3638fad21d17b7b3fc6b64d30d63</cites><orcidid>0000-0003-2947-1765 ; 0000-0003-0588-7256 ; 0000-0002-2168-5809</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035774/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7035774/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2100,2112,27922,27923,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32087719$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Konstantinidis, Alexandros</creatorcontrib><creatorcontrib>Pardali, Dimitra</creatorcontrib><creatorcontrib>Adamama-Moraitou, Katerina K.</creatorcontrib><creatorcontrib>Gazouli, Maria</creatorcontrib><creatorcontrib>Dovas, Chrysostomos I.</creatorcontrib><creatorcontrib>Legaki, Evangelia</creatorcontrib><creatorcontrib>Brellou, Georgia D.</creatorcontrib><creatorcontrib>Savvas, Ioannis</creatorcontrib><creatorcontrib>Jergens, Albert E.</creatorcontrib><creatorcontrib>Rallis, Timoleon S.</creatorcontrib><creatorcontrib>Allenspach, Karin</creatorcontrib><title>Colonic mucosal and serum expression of microRNAs in canine large intestinal inflammatory bowel disease</title><title>BMC veterinary research</title><addtitle>BMC VET RES</addtitle><addtitle>BMC Vet Res</addtitle><description>Background Canine inflammatory bowel disease (IBD) is a group of chronic gastrointestinal (GI) disorders of still largely unknown etiology. Canine IBD diagnosis is time-consuming and costly as other diseases with similar signs should be initially excluded. In human IBD microRNA (miR) expression changes have been reported in GI mucosa and blood. Thus, there is a possibility that miRs may provide insight into disease pathogenesis, diagnosis and even treatment of canine IBD. The aim of this study was to determine the colonic mucosal and serum relative expression of a miRs panel in dogs with large intestinal IBD and healthy control dogs. Results Compared to healthy control dogs, dogs with large intestinal IBD showed significantly increased relative expression of miR-16, miR-21, miR-122 and miR-147 in the colonic mucosa and serum, while the relative expression of miR-185, miR-192 and miR-223 was significantly decreased. Relative expression of miR-146a was significantly increased only in the serum of dogs with large intestinal IBD. Furthermore, serum miR-192 and miR-223 relative expression correlated to disease activity and endoscopic score, respectively. 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Canine IBD diagnosis is time-consuming and costly as other diseases with similar signs should be initially excluded. In human IBD microRNA (miR) expression changes have been reported in GI mucosa and blood. Thus, there is a possibility that miRs may provide insight into disease pathogenesis, diagnosis and even treatment of canine IBD. The aim of this study was to determine the colonic mucosal and serum relative expression of a miRs panel in dogs with large intestinal IBD and healthy control dogs. Results Compared to healthy control dogs, dogs with large intestinal IBD showed significantly increased relative expression of miR-16, miR-21, miR-122 and miR-147 in the colonic mucosa and serum, while the relative expression of miR-185, miR-192 and miR-223 was significantly decreased. Relative expression of miR-146a was significantly increased only in the serum of dogs with large intestinal IBD. Furthermore, serum miR-192 and miR-223 relative expression correlated to disease activity and endoscopic score, respectively. Conclusion Our data suggest the existence of dysregulated miRs expression patterns in canine IBD and support the potential future use of serum miRs as useful noninvasive biomarkers.</abstract><cop>LONDON</cop><pub>Springer Nature</pub><pmid>32087719</pmid><doi>10.1186/s12917-020-02287-6</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0003-2947-1765</orcidid><orcidid>https://orcid.org/0000-0003-0588-7256</orcidid><orcidid>https://orcid.org/0000-0002-2168-5809</orcidid><oa>free_for_read</oa></addata></record>
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subjects Apoptosis
Binding sites
Biomarker
Biomarkers
Colon
Colonoscopy
Dog
Inflammation
Inflammatory bowel disease
Inflammatory bowel diseases
Intestine
Leukemia
Life Sciences & Biomedicine
MicroRNAs
miRNA
Mucosa
Pathogenesis
Science & Technology
Studies
Tumor necrosis factor-TNF
Veterinary Sciences
title Colonic mucosal and serum expression of microRNAs in canine large intestinal inflammatory bowel disease
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