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Detection of Pathological Changes in the Aorta during Thoracic Aortic Aneurysm Progression on Molecular Level
The progression of thoracic aortic aneurysm depends on regulation of aortic wall homeostasis and on changes in the structural components of the extracellular matrix, which are affected by multiple molecular signalling pathways. We decided to correlate the diameter of ascending thoracic aneurysm with...
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Published in: | Disease markers 2017-01, Vol.2017 (2017), p.1-11 |
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creator | Marekova, Maria Sabol, František Rybár, Dušan Ferenčáková, Michaela Panagiotis, Artemiou Špaková, Ivana Urban, Peter Rabajdová, Miroslava Bobrov, Nikita |
description | The progression of thoracic aortic aneurysm depends on regulation of aortic wall homeostasis and on changes in the structural components of the extracellular matrix, which are affected by multiple molecular signalling pathways. We decided to correlate the diameter of ascending thoracic aneurysm with gene expression of inflammation markers (IL-6, CRP), cytokine receptors (IL-6R, TNFR1, and TNFR2), and extracellular matrix components (Emilin-1, MMP9, and TIMP) for detection of the degree of pathological process of TAA formation. The experimental group was divided into three groups according to the diameter of the aortic aneurysm. Whole blood and tissue samples were properly collected and used for nucleic acid, chromatin, and protein isolation. The mRNA levels were detected by qRT-PCR. For the detection of protein levels a Cytokine Array IV assay kit was used in combination with a biochip analyzer. In aortic tissue, significant positive correlations were found between increased mRNA levels of inflammatory cytokines (CRP and IL-6) on both mRNA levels in tissue and protein from the blood with maximum in stage 3. Changes of gene expression of selected genes can be used for the experimental study of the inflammatory receptor inhibitors during trials targeted on slowing down the progress of aortic wall aneurysm. |
doi_str_mv | 10.1155/2017/9185934 |
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We decided to correlate the diameter of ascending thoracic aneurysm with gene expression of inflammation markers (IL-6, CRP), cytokine receptors (IL-6R, TNFR1, and TNFR2), and extracellular matrix components (Emilin-1, MMP9, and TIMP) for detection of the degree of pathological process of TAA formation. The experimental group was divided into three groups according to the diameter of the aortic aneurysm. Whole blood and tissue samples were properly collected and used for nucleic acid, chromatin, and protein isolation. The mRNA levels were detected by qRT-PCR. For the detection of protein levels a Cytokine Array IV assay kit was used in combination with a biochip analyzer. In aortic tissue, significant positive correlations were found between increased mRNA levels of inflammatory cytokines (CRP and IL-6) on both mRNA levels in tissue and protein from the blood with maximum in stage 3. Changes of gene expression of selected genes can be used for the experimental study of the inflammatory receptor inhibitors during trials targeted on slowing down the progress of aortic wall aneurysm.</description><identifier>ISSN: 0278-0240</identifier><identifier>EISSN: 1875-8630</identifier><identifier>DOI: 10.1155/2017/9185934</identifier><identifier>PMID: 29158612</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Aneurysms ; Aorta ; Aortic aneurysms ; Biological markers ; Blood ; Change detection ; Chromatin ; Cytokine receptors ; Cytokines ; Development and progression ; Elastin microfibril interface located protein ; Extracellular matrix ; Gelatinase B ; Gene expression ; Genetic aspects ; Homeostasis ; Inflammation ; Interleukin 6 ; Nucleic acids ; Protein arrays ; Proteins ; Receptors ; Signal transduction ; Signaling ; Thorax ; Tissue inhibitor of metalloproteinases ; Tumor necrosis factor receptors</subject><ispartof>Disease markers, 2017-01, Vol.2017 (2017), p.1-11</ispartof><rights>Copyright © 2017 Miroslava Rabajdová et al.</rights><rights>COPYRIGHT 2017 John Wiley & Sons, Inc.</rights><rights>Copyright © 2017 Miroslava Rabajdová et al.; This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2017 Miroslava Rabajdová et al. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c565t-3c5bc97c724dcf7184e150b32f37b0ab14768e515b73342345da9eb2292812983</citedby><cites>FETCH-LOGICAL-c565t-3c5bc97c724dcf7184e150b32f37b0ab14768e515b73342345da9eb2292812983</cites><orcidid>0000-0003-2749-7953 ; 0000-0002-9103-4710</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,778,782,883,27911,27912</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29158612$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Shi, Zhongjie</contributor><contributor>Zhongjie Shi</contributor><creatorcontrib>Marekova, Maria</creatorcontrib><creatorcontrib>Sabol, František</creatorcontrib><creatorcontrib>Rybár, Dušan</creatorcontrib><creatorcontrib>Ferenčáková, Michaela</creatorcontrib><creatorcontrib>Panagiotis, Artemiou</creatorcontrib><creatorcontrib>Špaková, Ivana</creatorcontrib><creatorcontrib>Urban, Peter</creatorcontrib><creatorcontrib>Rabajdová, Miroslava</creatorcontrib><creatorcontrib>Bobrov, Nikita</creatorcontrib><title>Detection of Pathological Changes in the Aorta during Thoracic Aortic Aneurysm Progression on Molecular Level</title><title>Disease markers</title><addtitle>Dis Markers</addtitle><description>The progression of thoracic aortic aneurysm depends on regulation of aortic wall homeostasis and on changes in the structural components of the extracellular matrix, which are affected by multiple molecular signalling pathways. We decided to correlate the diameter of ascending thoracic aneurysm with gene expression of inflammation markers (IL-6, CRP), cytokine receptors (IL-6R, TNFR1, and TNFR2), and extracellular matrix components (Emilin-1, MMP9, and TIMP) for detection of the degree of pathological process of TAA formation. The experimental group was divided into three groups according to the diameter of the aortic aneurysm. Whole blood and tissue samples were properly collected and used for nucleic acid, chromatin, and protein isolation. The mRNA levels were detected by qRT-PCR. For the detection of protein levels a Cytokine Array IV assay kit was used in combination with a biochip analyzer. In aortic tissue, significant positive correlations were found between increased mRNA levels of inflammatory cytokines (CRP and IL-6) on both mRNA levels in tissue and protein from the blood with maximum in stage 3. Changes of gene expression of selected genes can be used for the experimental study of the inflammatory receptor inhibitors during trials targeted on slowing down the progress of aortic wall aneurysm.</description><subject>Aneurysms</subject><subject>Aorta</subject><subject>Aortic aneurysms</subject><subject>Biological markers</subject><subject>Blood</subject><subject>Change detection</subject><subject>Chromatin</subject><subject>Cytokine receptors</subject><subject>Cytokines</subject><subject>Development and progression</subject><subject>Elastin microfibril interface located protein</subject><subject>Extracellular matrix</subject><subject>Gelatinase B</subject><subject>Gene expression</subject><subject>Genetic aspects</subject><subject>Homeostasis</subject><subject>Inflammation</subject><subject>Interleukin 6</subject><subject>Nucleic acids</subject><subject>Protein arrays</subject><subject>Proteins</subject><subject>Receptors</subject><subject>Signal transduction</subject><subject>Signaling</subject><subject>Thorax</subject><subject>Tissue inhibitor of metalloproteinases</subject><subject>Tumor necrosis factor receptors</subject><issn>0278-0240</issn><issn>1875-8630</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqNkUFv1DAQRiMEokvhxhlZ4oJEQ20nju0L0mqhgLSIHsrZcpxJ4sprFzsp6r_H2V1a4MRppPHT83z6iuIlwe8IYeycYsLPJRFMVvWjYkUEZ6VoKvy4WGHKRYlpjU-KZyldY0yorOXT4oRKwkRD6KrYfYAJzGSDR6FHl3oagwuDNdqhzaj9AAlZj6YR0DrESaNujtYP6GoMURtr9ttleJjjXdqhyxiGCCnthR59DQ7M7HREW7gF97x40muX4MVxnhbfLz5ebT6X22-fvmzW29Kwhk1lZVhrJDec1p3pORE1EIbbivYVb7FuSc0bAYywlldVTauadVpCS6mkIkcU1Wnx_uC9mdsddAb8FLVTN9HudLxTQVv194u3oxrCrWJNgwWVWfDmKIjhxwxpUjubDDinPYQ5KSKbRkohMcvo63_Q6zBHn-OpXA0WzdLMAzVoB8r6PuR_zSJVa8ZyMwzv7z47UCaGlCL09ycTrJa2FyVXx7Yz_urPmPfw73oz8PYAjNZ3-qf9Tx1kBnr9QBNGmSDVL3oUuqU</recordid><startdate>20170101</startdate><enddate>20170101</enddate><creator>Marekova, Maria</creator><creator>Sabol, František</creator><creator>Rybár, Dušan</creator><creator>Ferenčáková, Michaela</creator><creator>Panagiotis, Artemiou</creator><creator>Špaková, Ivana</creator><creator>Urban, Peter</creator><creator>Rabajdová, Miroslava</creator><creator>Bobrov, Nikita</creator><general>Hindawi Publishing Corporation</general><general>Hindawi</general><general>John Wiley & Sons, Inc</general><general>Hindawi Limited</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7QO</scope><scope>7TK</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-2749-7953</orcidid><orcidid>https://orcid.org/0000-0002-9103-4710</orcidid></search><sort><creationdate>20170101</creationdate><title>Detection of Pathological Changes in the Aorta during Thoracic Aortic Aneurysm Progression on Molecular Level</title><author>Marekova, Maria ; Sabol, František ; Rybár, Dušan ; Ferenčáková, Michaela ; Panagiotis, Artemiou ; Špaková, Ivana ; Urban, Peter ; Rabajdová, Miroslava ; Bobrov, Nikita</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c565t-3c5bc97c724dcf7184e150b32f37b0ab14768e515b73342345da9eb2292812983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Aneurysms</topic><topic>Aorta</topic><topic>Aortic aneurysms</topic><topic>Biological markers</topic><topic>Blood</topic><topic>Change detection</topic><topic>Chromatin</topic><topic>Cytokine receptors</topic><topic>Cytokines</topic><topic>Development and progression</topic><topic>Elastin microfibril interface located protein</topic><topic>Extracellular matrix</topic><topic>Gelatinase B</topic><topic>Gene expression</topic><topic>Genetic aspects</topic><topic>Homeostasis</topic><topic>Inflammation</topic><topic>Interleukin 6</topic><topic>Nucleic acids</topic><topic>Protein arrays</topic><topic>Proteins</topic><topic>Receptors</topic><topic>Signal transduction</topic><topic>Signaling</topic><topic>Thorax</topic><topic>Tissue inhibitor of metalloproteinases</topic><topic>Tumor necrosis factor receptors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marekova, Maria</creatorcontrib><creatorcontrib>Sabol, František</creatorcontrib><creatorcontrib>Rybár, Dušan</creatorcontrib><creatorcontrib>Ferenčáková, Michaela</creatorcontrib><creatorcontrib>Panagiotis, Artemiou</creatorcontrib><creatorcontrib>Špaková, Ivana</creatorcontrib><creatorcontrib>Urban, Peter</creatorcontrib><creatorcontrib>Rabajdová, Miroslava</creatorcontrib><creatorcontrib>Bobrov, Nikita</creatorcontrib><collection>الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals</collection><collection>معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete</collection><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Disease markers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marekova, Maria</au><au>Sabol, František</au><au>Rybár, Dušan</au><au>Ferenčáková, Michaela</au><au>Panagiotis, Artemiou</au><au>Špaková, Ivana</au><au>Urban, Peter</au><au>Rabajdová, Miroslava</au><au>Bobrov, Nikita</au><au>Shi, Zhongjie</au><au>Zhongjie Shi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detection of Pathological Changes in the Aorta during Thoracic Aortic Aneurysm Progression on Molecular Level</atitle><jtitle>Disease markers</jtitle><addtitle>Dis Markers</addtitle><date>2017-01-01</date><risdate>2017</risdate><volume>2017</volume><issue>2017</issue><spage>1</spage><epage>11</epage><pages>1-11</pages><issn>0278-0240</issn><eissn>1875-8630</eissn><abstract>The progression of thoracic aortic aneurysm depends on regulation of aortic wall homeostasis and on changes in the structural components of the extracellular matrix, which are affected by multiple molecular signalling pathways. 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Changes of gene expression of selected genes can be used for the experimental study of the inflammatory receptor inhibitors during trials targeted on slowing down the progress of aortic wall aneurysm.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>29158612</pmid><doi>10.1155/2017/9185934</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-2749-7953</orcidid><orcidid>https://orcid.org/0000-0002-9103-4710</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aneurysms Aorta Aortic aneurysms Biological markers Blood Change detection Chromatin Cytokine receptors Cytokines Development and progression Elastin microfibril interface located protein Extracellular matrix Gelatinase B Gene expression Genetic aspects Homeostasis Inflammation Interleukin 6 Nucleic acids Protein arrays Proteins Receptors Signal transduction Signaling Thorax Tissue inhibitor of metalloproteinases Tumor necrosis factor receptors |
title | Detection of Pathological Changes in the Aorta during Thoracic Aortic Aneurysm Progression on Molecular Level |
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