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Identification of an up-regulated anti-apoptotic network in the internal thoracic artery
Abstract Background The radial artery (RA) is known as an atherosclerosis-prone vessel in contrast to the atherosclerosis-resistant internal thoracic artery (ITA). The purpose of the present study was to compare the gene expression profile of these arteries from the same patient in order to identify...
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Published in: | International journal of cardiology 2011-06, Vol.149 (2), p.221-226 |
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creator | Krane, Markus Dummler, Sara Dreßen, Martina Hauner, Hans Hoffmann, Micha Haller, Dirk Heller, Katharina Wildhirt, Stephen Voss, Bernhard Grammer, Joachim Lahm, Harald Lange, Rüdiger Bauernschmitt, Robert |
description | Abstract Background The radial artery (RA) is known as an atherosclerosis-prone vessel in contrast to the atherosclerosis-resistant internal thoracic artery (ITA). The purpose of the present study was to compare the gene expression profile of these arteries from the same patient in order to identify genes involved in atherogenesis or intimal hyperplasia. Methods Paired specimens of RA and ITA ( n = 6) were analyzed by histomorphometry and whole genome microarray. The microarray data underwent pathway analysis to identify biological networks. Laser microdissection (LMD) was used to identify the cellular expression of candidate genes in the intimal or medial layer of the ITA and RA. Results Histomorphometric analyses revealed a significantly higher degree of intimal hyperplasia in the RA compared to the ITA. 552 genes were differentially expressed in the ITA and RA. qRT-PCR confirmed a significant up-regulation of six anti-apoptotic genes. p21 (11.8-fold, p = 0.011), CCL2 (5.4-fold, p = 0.034), SOCS3 (7.2-fold, p = 0.002), IER3 (4.1-fold, p = 0.048), MCL-1 (2.6-fold, p = 0.025) and IL-6 (17.8-fold, p = 0.046) were up-regulated in the ITA. LMD confirmed that cells of the intimal layer of the ITA consistently expressed higher levels of all six candidate genes than those of the RA. Conclusions Microarray analysis and qRT-PCR identified significantly up-regulated genes in the ITA involved in an anti-apoptotic network. LMD revealed a higher expression of all anti-apoptotic genes in the intimal area of the ITA. These genes may play an important role in protecting the intima of the ITA from developing hyperplasia and atherosclerosis. |
doi_str_mv | 10.1016/j.ijcard.2010.02.003 |
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The purpose of the present study was to compare the gene expression profile of these arteries from the same patient in order to identify genes involved in atherogenesis or intimal hyperplasia. Methods Paired specimens of RA and ITA ( n = 6) were analyzed by histomorphometry and whole genome microarray. The microarray data underwent pathway analysis to identify biological networks. Laser microdissection (LMD) was used to identify the cellular expression of candidate genes in the intimal or medial layer of the ITA and RA. Results Histomorphometric analyses revealed a significantly higher degree of intimal hyperplasia in the RA compared to the ITA. 552 genes were differentially expressed in the ITA and RA. qRT-PCR confirmed a significant up-regulation of six anti-apoptotic genes. p21 (11.8-fold, p = 0.011), CCL2 (5.4-fold, p = 0.034), SOCS3 (7.2-fold, p = 0.002), IER3 (4.1-fold, p = 0.048), MCL-1 (2.6-fold, p = 0.025) and IL-6 (17.8-fold, p = 0.046) were up-regulated in the ITA. LMD confirmed that cells of the intimal layer of the ITA consistently expressed higher levels of all six candidate genes than those of the RA. Conclusions Microarray analysis and qRT-PCR identified significantly up-regulated genes in the ITA involved in an anti-apoptotic network. LMD revealed a higher expression of all anti-apoptotic genes in the intimal area of the ITA. These genes may play an important role in protecting the intima of the ITA from developing hyperplasia and atherosclerosis.</description><identifier>ISSN: 0167-5273</identifier><identifier>EISSN: 1874-1754</identifier><identifier>DOI: 10.1016/j.ijcard.2010.02.003</identifier><identifier>PMID: 20207035</identifier><identifier>CODEN: IJCDD5</identifier><language>eng</language><publisher>Shannon: Elsevier B.V</publisher><subject>Aged ; Aged, 80 and over ; Anti-apoptosis ; Apoptosis - genetics ; Apoptosis - physiology ; Atherosclerosis ; Atherosclerosis (general aspects, experimental research) ; Biological and medical sciences ; Blood and lymphatic vessels ; Cardiology. Vascular system ; Cardiovascular ; Coronary Artery Bypass - methods ; Gene expression ; Gene Regulatory Networks - physiology ; Humans ; Internal thoracic artery ; Intimal hyperplasia ; Mammary Arteries - physiology ; Medical sciences ; Microarray Analysis - methods ; Middle Aged ; Radial artery ; Up-Regulation - genetics ; Up-Regulation - physiology</subject><ispartof>International journal of cardiology, 2011-06, Vol.149 (2), p.221-226</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2010 Elsevier Ireland Ltd</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c512t-4a770930c2bf774dff6d33c6850e43804b5d8dd9909632d0e116ea07720636a03</citedby><cites>FETCH-LOGICAL-c512t-4a770930c2bf774dff6d33c6850e43804b5d8dd9909632d0e116ea07720636a03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24259900$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20207035$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Krane, Markus</creatorcontrib><creatorcontrib>Dummler, Sara</creatorcontrib><creatorcontrib>Dreßen, Martina</creatorcontrib><creatorcontrib>Hauner, Hans</creatorcontrib><creatorcontrib>Hoffmann, Micha</creatorcontrib><creatorcontrib>Haller, Dirk</creatorcontrib><creatorcontrib>Heller, Katharina</creatorcontrib><creatorcontrib>Wildhirt, Stephen</creatorcontrib><creatorcontrib>Voss, Bernhard</creatorcontrib><creatorcontrib>Grammer, Joachim</creatorcontrib><creatorcontrib>Lahm, Harald</creatorcontrib><creatorcontrib>Lange, Rüdiger</creatorcontrib><creatorcontrib>Bauernschmitt, Robert</creatorcontrib><title>Identification of an up-regulated anti-apoptotic network in the internal thoracic artery</title><title>International journal of cardiology</title><addtitle>Int J Cardiol</addtitle><description>Abstract Background The radial artery (RA) is known as an atherosclerosis-prone vessel in contrast to the atherosclerosis-resistant internal thoracic artery (ITA). The purpose of the present study was to compare the gene expression profile of these arteries from the same patient in order to identify genes involved in atherogenesis or intimal hyperplasia. Methods Paired specimens of RA and ITA ( n = 6) were analyzed by histomorphometry and whole genome microarray. The microarray data underwent pathway analysis to identify biological networks. Laser microdissection (LMD) was used to identify the cellular expression of candidate genes in the intimal or medial layer of the ITA and RA. Results Histomorphometric analyses revealed a significantly higher degree of intimal hyperplasia in the RA compared to the ITA. 552 genes were differentially expressed in the ITA and RA. qRT-PCR confirmed a significant up-regulation of six anti-apoptotic genes. p21 (11.8-fold, p = 0.011), CCL2 (5.4-fold, p = 0.034), SOCS3 (7.2-fold, p = 0.002), IER3 (4.1-fold, p = 0.048), MCL-1 (2.6-fold, p = 0.025) and IL-6 (17.8-fold, p = 0.046) were up-regulated in the ITA. LMD confirmed that cells of the intimal layer of the ITA consistently expressed higher levels of all six candidate genes than those of the RA. Conclusions Microarray analysis and qRT-PCR identified significantly up-regulated genes in the ITA involved in an anti-apoptotic network. LMD revealed a higher expression of all anti-apoptotic genes in the intimal area of the ITA. These genes may play an important role in protecting the intima of the ITA from developing hyperplasia and atherosclerosis.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anti-apoptosis</subject><subject>Apoptosis - genetics</subject><subject>Apoptosis - physiology</subject><subject>Atherosclerosis</subject><subject>Atherosclerosis (general aspects, experimental research)</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Cardiology. Vascular system</subject><subject>Cardiovascular</subject><subject>Coronary Artery Bypass - methods</subject><subject>Gene expression</subject><subject>Gene Regulatory Networks - physiology</subject><subject>Humans</subject><subject>Internal thoracic artery</subject><subject>Intimal hyperplasia</subject><subject>Mammary Arteries - physiology</subject><subject>Medical sciences</subject><subject>Microarray Analysis - methods</subject><subject>Middle Aged</subject><subject>Radial artery</subject><subject>Up-Regulation - genetics</subject><subject>Up-Regulation - physiology</subject><issn>0167-5273</issn><issn>1874-1754</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqFkU-LFDEQxYMo7uzqNxDpi3jqsfKnk-6LIIu6CwseVPAWMkm1ZrYnaZO0Mt_eNDMqePFUVPGrqsd7hDyjsKVA5av91u-tSW7LoI6AbQH4A7KhvRItVZ14SDYVU23HFL8glznvAUAMQ_-YXDBgoIB3G_Ll1mEofvTWFB9DE8fGhGaZ24Rfl8kUdLUvvjVznEss3jYBy8-Y7hsfmvINaymYgplqE5OxFTCpTo5PyKPRTBmfnusV-fzu7afrm_buw_vb6zd3re0oK60wSsHAwbLdqJRw4ygd51b2HaDgPYhd53rnhgEGyZkDpFSiAaUYSC4N8Cvy8nR3TvH7grnog88Wp8kEjEvWvZK078TAKilOpE0x54SjnpM_mHTUFPRqqd7rk6V6tVQD09XSuvb8_GDZHdD9WfrtYQVenAGTrZnGZIL1-S8nWFflr0pfnzisdvzwmHS2HoNF5xPaol30_1Py7wE7-VCTm-7xiHkflzWIrKnOdUF_XONf06c1eJCy478Ak8Oqgg</recordid><startdate>20110602</startdate><enddate>20110602</enddate><creator>Krane, Markus</creator><creator>Dummler, Sara</creator><creator>Dreßen, Martina</creator><creator>Hauner, Hans</creator><creator>Hoffmann, Micha</creator><creator>Haller, Dirk</creator><creator>Heller, Katharina</creator><creator>Wildhirt, Stephen</creator><creator>Voss, Bernhard</creator><creator>Grammer, Joachim</creator><creator>Lahm, Harald</creator><creator>Lange, Rüdiger</creator><creator>Bauernschmitt, Robert</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><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>20110602</creationdate><title>Identification of an up-regulated anti-apoptotic network in the internal thoracic artery</title><author>Krane, Markus ; Dummler, Sara ; Dreßen, Martina ; Hauner, Hans ; Hoffmann, Micha ; Haller, Dirk ; Heller, Katharina ; Wildhirt, Stephen ; Voss, Bernhard ; Grammer, Joachim ; Lahm, Harald ; Lange, Rüdiger ; Bauernschmitt, Robert</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c512t-4a770930c2bf774dff6d33c6850e43804b5d8dd9909632d0e116ea07720636a03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Anti-apoptosis</topic><topic>Apoptosis - genetics</topic><topic>Apoptosis - physiology</topic><topic>Atherosclerosis</topic><topic>Atherosclerosis (general aspects, experimental research)</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Cardiology. Vascular system</topic><topic>Cardiovascular</topic><topic>Coronary Artery Bypass - methods</topic><topic>Gene expression</topic><topic>Gene Regulatory Networks - physiology</topic><topic>Humans</topic><topic>Internal thoracic artery</topic><topic>Intimal hyperplasia</topic><topic>Mammary Arteries - physiology</topic><topic>Medical sciences</topic><topic>Microarray Analysis - methods</topic><topic>Middle Aged</topic><topic>Radial artery</topic><topic>Up-Regulation - genetics</topic><topic>Up-Regulation - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Krane, Markus</creatorcontrib><creatorcontrib>Dummler, Sara</creatorcontrib><creatorcontrib>Dreßen, Martina</creatorcontrib><creatorcontrib>Hauner, Hans</creatorcontrib><creatorcontrib>Hoffmann, Micha</creatorcontrib><creatorcontrib>Haller, Dirk</creatorcontrib><creatorcontrib>Heller, Katharina</creatorcontrib><creatorcontrib>Wildhirt, Stephen</creatorcontrib><creatorcontrib>Voss, Bernhard</creatorcontrib><creatorcontrib>Grammer, Joachim</creatorcontrib><creatorcontrib>Lahm, Harald</creatorcontrib><creatorcontrib>Lange, Rüdiger</creatorcontrib><creatorcontrib>Bauernschmitt, Robert</creatorcontrib><collection>Pascal-Francis</collection><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>International journal of cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Krane, Markus</au><au>Dummler, Sara</au><au>Dreßen, Martina</au><au>Hauner, Hans</au><au>Hoffmann, Micha</au><au>Haller, Dirk</au><au>Heller, Katharina</au><au>Wildhirt, Stephen</au><au>Voss, Bernhard</au><au>Grammer, Joachim</au><au>Lahm, Harald</au><au>Lange, Rüdiger</au><au>Bauernschmitt, Robert</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of an up-regulated anti-apoptotic network in the internal thoracic artery</atitle><jtitle>International journal of cardiology</jtitle><addtitle>Int J Cardiol</addtitle><date>2011-06-02</date><risdate>2011</risdate><volume>149</volume><issue>2</issue><spage>221</spage><epage>226</epage><pages>221-226</pages><issn>0167-5273</issn><eissn>1874-1754</eissn><coden>IJCDD5</coden><abstract>Abstract Background The radial artery (RA) is known as an atherosclerosis-prone vessel in contrast to the atherosclerosis-resistant internal thoracic artery (ITA). The purpose of the present study was to compare the gene expression profile of these arteries from the same patient in order to identify genes involved in atherogenesis or intimal hyperplasia. Methods Paired specimens of RA and ITA ( n = 6) were analyzed by histomorphometry and whole genome microarray. The microarray data underwent pathway analysis to identify biological networks. Laser microdissection (LMD) was used to identify the cellular expression of candidate genes in the intimal or medial layer of the ITA and RA. Results Histomorphometric analyses revealed a significantly higher degree of intimal hyperplasia in the RA compared to the ITA. 552 genes were differentially expressed in the ITA and RA. qRT-PCR confirmed a significant up-regulation of six anti-apoptotic genes. p21 (11.8-fold, p = 0.011), CCL2 (5.4-fold, p = 0.034), SOCS3 (7.2-fold, p = 0.002), IER3 (4.1-fold, p = 0.048), MCL-1 (2.6-fold, p = 0.025) and IL-6 (17.8-fold, p = 0.046) were up-regulated in the ITA. LMD confirmed that cells of the intimal layer of the ITA consistently expressed higher levels of all six candidate genes than those of the RA. Conclusions Microarray analysis and qRT-PCR identified significantly up-regulated genes in the ITA involved in an anti-apoptotic network. LMD revealed a higher expression of all anti-apoptotic genes in the intimal area of the ITA. These genes may play an important role in protecting the intima of the ITA from developing hyperplasia and atherosclerosis.</abstract><cop>Shannon</cop><pub>Elsevier B.V</pub><pmid>20207035</pmid><doi>10.1016/j.ijcard.2010.02.003</doi><tpages>6</tpages></addata></record> |
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subjects | Aged Aged, 80 and over Anti-apoptosis Apoptosis - genetics Apoptosis - physiology Atherosclerosis Atherosclerosis (general aspects, experimental research) Biological and medical sciences Blood and lymphatic vessels Cardiology. Vascular system Cardiovascular Coronary Artery Bypass - methods Gene expression Gene Regulatory Networks - physiology Humans Internal thoracic artery Intimal hyperplasia Mammary Arteries - physiology Medical sciences Microarray Analysis - methods Middle Aged Radial artery Up-Regulation - genetics Up-Regulation - physiology |
title | Identification of an up-regulated anti-apoptotic network in the internal thoracic artery |
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