Methylation of MMP2, TIMP2, MMP9 and TIMP1 in abdominal aortic aneurysm
Abdominal aortic aneurysm (AAA) and its complications are among the most serious cardiovascular diseases and its occurrence has risen sharply in recent years. The aim of this pilot study is to explore the relationship between the methylation of matrix metalloproteinases and tissue inhibitors of the...
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Veröffentlicht in: | Bratislava Medical Journal 2020, Vol.121 (10), p.717-721 |
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creator | Skorvanova, M Matakova, T Skerenova, M Sarlinova, M Drobkova, H Petras, M Janickova, M Halasa, M Repiska, V Halasova, E |
description | Abdominal aortic aneurysm (AAA) and its complications are among the most serious cardiovascular diseases and its occurrence has risen sharply in recent years. The aim of this pilot study is to explore the relationship between the methylation of matrix metalloproteinases and tissue inhibitors of the metalloproteinases genes' promoter region, and abdominal aortic aneurysm (AAA) through the detection of the methylation status of MMP2, TIMP2, TIMP1, and MMP9 genes in peripheral blood.
The study included 43 males with verified AAA (case group) and 34 healthy males (control group). The methylation status of the genes' promoter region was detected by methylation-specific polymerase chain reaction (MS-PCR).
In adominal aortic aneurysm patients, the methylation ratio of MMP2 gene was positive in 9.3 % (4 cases), 2.3 % (1 case) had methylated TIMP2 gene, 7.0 % (3 cases) had methylated TIMP1 gene, while the methylation ratio of MMP9 gene was positive in 93.0 % (40 cases). In the control group, MMP2 gene was found to be methylated in 5.9 % (2 cases), 5.9 % of cases had methylated TIMP2 and TIMP1 genes (2 cases), and MMP9 gene was found to be methylated in 91.2 % (31 cases).
In our pilot study, we found no association between DNA methylation of gelatinases and their tissue inhibitors, and the development of an abdominal aortic aneurysm (Tab. 2, Fig. 1, Ref. 27). |
doi_str_mv | 10.4149/BLL_2020_117 |
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The study included 43 males with verified AAA (case group) and 34 healthy males (control group). The methylation status of the genes' promoter region was detected by methylation-specific polymerase chain reaction (MS-PCR).
In adominal aortic aneurysm patients, the methylation ratio of MMP2 gene was positive in 9.3 % (4 cases), 2.3 % (1 case) had methylated TIMP2 gene, 7.0 % (3 cases) had methylated TIMP1 gene, while the methylation ratio of MMP9 gene was positive in 93.0 % (40 cases). In the control group, MMP2 gene was found to be methylated in 5.9 % (2 cases), 5.9 % of cases had methylated TIMP2 and TIMP1 genes (2 cases), and MMP9 gene was found to be methylated in 91.2 % (31 cases).
In our pilot study, we found no association between DNA methylation of gelatinases and their tissue inhibitors, and the development of an abdominal aortic aneurysm (Tab. 2, Fig. 1, Ref. 27).</description><identifier>ISSN: 0006-9248</identifier><identifier>ISSN: 1336-0345</identifier><identifier>EISSN: 1336-0345</identifier><identifier>DOI: 10.4149/BLL_2020_117</identifier><identifier>PMID: 32955903</identifier><language>eng</language><publisher>Slovakia</publisher><subject>Aortic Aneurysm, Abdominal - genetics ; DNA Methylation ; Humans ; Male ; Matrix Metalloproteinase 2 - genetics ; Matrix Metalloproteinase 2 - metabolism ; Matrix Metalloproteinase 9 - genetics ; Matrix Metalloproteinase 9 - metabolism ; Matrix Metalloproteinases ; Pilot Projects ; Tissue Inhibitor of Metalloproteinase-1 - genetics ; Tissue Inhibitor of Metalloproteinase-1 - metabolism ; Tissue Inhibitor of Metalloproteinase-2 - genetics ; Tissue Inhibitor of Metalloproteinase-2 - metabolism</subject><ispartof>Bratislava Medical Journal, 2020, Vol.121 (10), p.717-721</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c329t-440b404d5c83c885ff2b069a60961db844f0fa4854ec24ce409db196866a3cb23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4009,27902,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32955903$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Skorvanova, M</creatorcontrib><creatorcontrib>Matakova, T</creatorcontrib><creatorcontrib>Skerenova, M</creatorcontrib><creatorcontrib>Sarlinova, M</creatorcontrib><creatorcontrib>Drobkova, H</creatorcontrib><creatorcontrib>Petras, M</creatorcontrib><creatorcontrib>Janickova, M</creatorcontrib><creatorcontrib>Halasa, M</creatorcontrib><creatorcontrib>Repiska, V</creatorcontrib><creatorcontrib>Halasova, E</creatorcontrib><title>Methylation of MMP2, TIMP2, MMP9 and TIMP1 in abdominal aortic aneurysm</title><title>Bratislava Medical Journal</title><addtitle>Bratisl Lek Listy</addtitle><description>Abdominal aortic aneurysm (AAA) and its complications are among the most serious cardiovascular diseases and its occurrence has risen sharply in recent years. The aim of this pilot study is to explore the relationship between the methylation of matrix metalloproteinases and tissue inhibitors of the metalloproteinases genes' promoter region, and abdominal aortic aneurysm (AAA) through the detection of the methylation status of MMP2, TIMP2, TIMP1, and MMP9 genes in peripheral blood.
The study included 43 males with verified AAA (case group) and 34 healthy males (control group). The methylation status of the genes' promoter region was detected by methylation-specific polymerase chain reaction (MS-PCR).
In adominal aortic aneurysm patients, the methylation ratio of MMP2 gene was positive in 9.3 % (4 cases), 2.3 % (1 case) had methylated TIMP2 gene, 7.0 % (3 cases) had methylated TIMP1 gene, while the methylation ratio of MMP9 gene was positive in 93.0 % (40 cases). In the control group, MMP2 gene was found to be methylated in 5.9 % (2 cases), 5.9 % of cases had methylated TIMP2 and TIMP1 genes (2 cases), and MMP9 gene was found to be methylated in 91.2 % (31 cases).
In our pilot study, we found no association between DNA methylation of gelatinases and their tissue inhibitors, and the development of an abdominal aortic aneurysm (Tab. 2, Fig. 1, Ref. 27).</description><subject>Aortic Aneurysm, Abdominal - genetics</subject><subject>DNA Methylation</subject><subject>Humans</subject><subject>Male</subject><subject>Matrix Metalloproteinase 2 - genetics</subject><subject>Matrix Metalloproteinase 2 - metabolism</subject><subject>Matrix Metalloproteinase 9 - genetics</subject><subject>Matrix Metalloproteinase 9 - metabolism</subject><subject>Matrix Metalloproteinases</subject><subject>Pilot Projects</subject><subject>Tissue Inhibitor of Metalloproteinase-1 - genetics</subject><subject>Tissue Inhibitor of Metalloproteinase-1 - metabolism</subject><subject>Tissue Inhibitor of Metalloproteinase-2 - genetics</subject><subject>Tissue Inhibitor of Metalloproteinase-2 - metabolism</subject><issn>0006-9248</issn><issn>1336-0345</issn><issn>1336-0345</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkL1PwzAUxC0EoqWwMaOMDA082y_GHqGCUikVDGW2HMcRQUlc4mTIf0_6AWI6nd5Pd09HyDWFO6So7p_SVDNgoCl9OCFTyrmIgWNySqYAIGLFUE7IRQhfAMgTKs7JhDOVJAr4lCzXrvscKtOVvol8Ea3X72webVZ7GY2KTJPvPY3KJjJZ7uuyMVVkfNuVdry6vh1CfUnOClMFd3XUGfl4ed4sXuP0bblaPKaxHTu7GBEyBMwTK7mVMikKloFQRoASNM8kYgGFQZmgswytQ1B5RpWQQhhuM8Zn5PaQu239d-9Cp-syWFdV4yO-D5ohopRMiB06P6C29SG0rtDbtqxNO2gKejed_j_diN8ck_usdvkf_LsV_wFMpmW8</recordid><startdate>2020</startdate><enddate>2020</enddate><creator>Skorvanova, M</creator><creator>Matakova, T</creator><creator>Skerenova, M</creator><creator>Sarlinova, M</creator><creator>Drobkova, H</creator><creator>Petras, M</creator><creator>Janickova, M</creator><creator>Halasa, M</creator><creator>Repiska, V</creator><creator>Halasova, E</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>2020</creationdate><title>Methylation of MMP2, TIMP2, MMP9 and TIMP1 in abdominal aortic aneurysm</title><author>Skorvanova, M ; Matakova, T ; Skerenova, M ; Sarlinova, M ; Drobkova, H ; Petras, M ; Janickova, M ; Halasa, M ; Repiska, V ; Halasova, E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c329t-440b404d5c83c885ff2b069a60961db844f0fa4854ec24ce409db196866a3cb23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Aortic Aneurysm, Abdominal - genetics</topic><topic>DNA Methylation</topic><topic>Humans</topic><topic>Male</topic><topic>Matrix Metalloproteinase 2 - genetics</topic><topic>Matrix Metalloproteinase 2 - metabolism</topic><topic>Matrix Metalloproteinase 9 - genetics</topic><topic>Matrix Metalloproteinase 9 - metabolism</topic><topic>Matrix Metalloproteinases</topic><topic>Pilot Projects</topic><topic>Tissue Inhibitor of Metalloproteinase-1 - genetics</topic><topic>Tissue Inhibitor of Metalloproteinase-1 - metabolism</topic><topic>Tissue Inhibitor of Metalloproteinase-2 - genetics</topic><topic>Tissue Inhibitor of Metalloproteinase-2 - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Skorvanova, M</creatorcontrib><creatorcontrib>Matakova, T</creatorcontrib><creatorcontrib>Skerenova, M</creatorcontrib><creatorcontrib>Sarlinova, M</creatorcontrib><creatorcontrib>Drobkova, H</creatorcontrib><creatorcontrib>Petras, M</creatorcontrib><creatorcontrib>Janickova, M</creatorcontrib><creatorcontrib>Halasa, M</creatorcontrib><creatorcontrib>Repiska, V</creatorcontrib><creatorcontrib>Halasova, E</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Bratislava Medical Journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Skorvanova, M</au><au>Matakova, T</au><au>Skerenova, M</au><au>Sarlinova, M</au><au>Drobkova, H</au><au>Petras, M</au><au>Janickova, M</au><au>Halasa, M</au><au>Repiska, V</au><au>Halasova, E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Methylation of MMP2, TIMP2, MMP9 and TIMP1 in abdominal aortic aneurysm</atitle><jtitle>Bratislava Medical Journal</jtitle><addtitle>Bratisl Lek Listy</addtitle><date>2020</date><risdate>2020</risdate><volume>121</volume><issue>10</issue><spage>717</spage><epage>721</epage><pages>717-721</pages><issn>0006-9248</issn><issn>1336-0345</issn><eissn>1336-0345</eissn><abstract>Abdominal aortic aneurysm (AAA) and its complications are among the most serious cardiovascular diseases and its occurrence has risen sharply in recent years. The aim of this pilot study is to explore the relationship between the methylation of matrix metalloproteinases and tissue inhibitors of the metalloproteinases genes' promoter region, and abdominal aortic aneurysm (AAA) through the detection of the methylation status of MMP2, TIMP2, TIMP1, and MMP9 genes in peripheral blood.
The study included 43 males with verified AAA (case group) and 34 healthy males (control group). The methylation status of the genes' promoter region was detected by methylation-specific polymerase chain reaction (MS-PCR).
In adominal aortic aneurysm patients, the methylation ratio of MMP2 gene was positive in 9.3 % (4 cases), 2.3 % (1 case) had methylated TIMP2 gene, 7.0 % (3 cases) had methylated TIMP1 gene, while the methylation ratio of MMP9 gene was positive in 93.0 % (40 cases). In the control group, MMP2 gene was found to be methylated in 5.9 % (2 cases), 5.9 % of cases had methylated TIMP2 and TIMP1 genes (2 cases), and MMP9 gene was found to be methylated in 91.2 % (31 cases).
In our pilot study, we found no association between DNA methylation of gelatinases and their tissue inhibitors, and the development of an abdominal aortic aneurysm (Tab. 2, Fig. 1, Ref. 27).</abstract><cop>Slovakia</cop><pmid>32955903</pmid><doi>10.4149/BLL_2020_117</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aortic Aneurysm, Abdominal - genetics DNA Methylation Humans Male Matrix Metalloproteinase 2 - genetics Matrix Metalloproteinase 2 - metabolism Matrix Metalloproteinase 9 - genetics Matrix Metalloproteinase 9 - metabolism Matrix Metalloproteinases Pilot Projects Tissue Inhibitor of Metalloproteinase-1 - genetics Tissue Inhibitor of Metalloproteinase-1 - metabolism Tissue Inhibitor of Metalloproteinase-2 - genetics Tissue Inhibitor of Metalloproteinase-2 - metabolism |
title | Methylation of MMP2, TIMP2, MMP9 and TIMP1 in abdominal aortic aneurysm |
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