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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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. |
doi_str_mv | 10.1186/s12917-020-02287-6 |
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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 & Biomedicine ; MicroRNAs ; miRNA ; Mucosa ; Pathogenesis ; Science & 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. 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><subject>Apoptosis</subject><subject>Binding sites</subject><subject>Biomarker</subject><subject>Biomarkers</subject><subject>Colon</subject><subject>Colonoscopy</subject><subject>Dog</subject><subject>Inflammation</subject><subject>Inflammatory bowel disease</subject><subject>Inflammatory bowel diseases</subject><subject>Intestine</subject><subject>Leukemia</subject><subject>Life Sciences & Biomedicine</subject><subject>MicroRNAs</subject><subject>miRNA</subject><subject>Mucosa</subject><subject>Pathogenesis</subject><subject>Science & Technology</subject><subject>Studies</subject><subject>Tumor necrosis factor-TNF</subject><subject>Veterinary Sciences</subject><issn>1746-6148</issn><issn>1746-6148</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>AOWDO</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>DOA</sourceid><recordid>eNqNUk1v1DAUjBCIlsIf4IAscUFCgefY8ccFqYooVKpAQnC2HMdevErsxU4o_ff1bsqq5cTBev6YGfuNp6peYniHsWDvM24k5jU0UEYjeM0eVaeYU1YzTMXje_OT6lnOWwBKJWdPqxPSgOAcy9Nq08UxBm_QtJiY9Yh0GFC2aZmQ_bNLNmcfA4oOTd6k-O3LeUY-IKODDxaNOm1sWc82zz4Usg9u1NOk55huUB-v7YgGn63O9nn1xOkx2xd39az6cfHxe_e5vvr66bI7v6oNlWyuHbQDc8QQpymRTd9KLig1grZCiL4UaUxPGBFODw0eMO95T5xhPaMDgYGRs-py1R2i3qpd8pNONypqrw4bMW2UTrM3o1XcFB0L3AHV9HCj2LsIIB3F2Lmi9WHV2i39ZAdjw5z0-ED04UnwP9Um_lYcSMs5LQJv7gRS_LUUk9Tks7HjqIONS1ZN6QSoEIAL9PU_0G1cUvF0j-ISRCuhKahmRZW_yDlZd3wMBrXPhFozoUom1CETam_Jq_ttHCl_Q1AAYgVc2z66bLwNxh5hANBiThrWlhngzs96Lpno4hLmQn37_1RyC1_n050</recordid><startdate>20200222</startdate><enddate>20200222</enddate><creator>Konstantinidis, Alexandros</creator><creator>Pardali, Dimitra</creator><creator>Adamama-Moraitou, Katerina K.</creator><creator>Gazouli, Maria</creator><creator>Dovas, Chrysostomos I.</creator><creator>Legaki, Evangelia</creator><creator>Brellou, Georgia D.</creator><creator>Savvas, Ioannis</creator><creator>Jergens, Albert E.</creator><creator>Rallis, Timoleon S.</creator><creator>Allenspach, Karin</creator><general>Springer Nature</general><general>BioMed Central</general><general>BMC</general><scope>AOWDO</scope><scope>BLEPL</scope><scope>DTL</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QG</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><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></search><sort><creationdate>20200222</creationdate><title>Colonic mucosal and serum expression of microRNAs in canine large intestinal inflammatory bowel disease</title><author>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</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c496t-f05d6f3c3fa4392b597844c845888b8459ccb3638fad21d17b7b3fc6b64d30d63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Apoptosis</topic><topic>Binding sites</topic><topic>Biomarker</topic><topic>Biomarkers</topic><topic>Colon</topic><topic>Colonoscopy</topic><topic>Dog</topic><topic>Inflammation</topic><topic>Inflammatory bowel disease</topic><topic>Inflammatory bowel diseases</topic><topic>Intestine</topic><topic>Leukemia</topic><topic>Life Sciences & Biomedicine</topic><topic>MicroRNAs</topic><topic>miRNA</topic><topic>Mucosa</topic><topic>Pathogenesis</topic><topic>Science & Technology</topic><topic>Studies</topic><topic>Tumor necrosis factor-TNF</topic><topic>Veterinary Sciences</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>Web of Science - Science Citation Index Expanded - 2020</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>BMC veterinary research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Konstantinidis, Alexandros</au><au>Pardali, Dimitra</au><au>Adamama-Moraitou, Katerina K.</au><au>Gazouli, Maria</au><au>Dovas, Chrysostomos I.</au><au>Legaki, Evangelia</au><au>Brellou, Georgia D.</au><au>Savvas, Ioannis</au><au>Jergens, Albert E.</au><au>Rallis, Timoleon S.</au><au>Allenspach, Karin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Colonic mucosal and serum expression of microRNAs in canine large intestinal inflammatory bowel disease</atitle><jtitle>BMC veterinary research</jtitle><stitle>BMC VET RES</stitle><addtitle>BMC Vet Res</addtitle><date>2020-02-22</date><risdate>2020</risdate><volume>16</volume><issue>1</issue><spage>69</spage><epage>69</epage><pages>69-69</pages><artnum>69</artnum><issn>1746-6148</issn><eissn>1746-6148</eissn><abstract>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.</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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