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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
Main Authors: 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
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cited_by cdi_FETCH-LOGICAL-c512t-4a770930c2bf774dff6d33c6850e43804b5d8dd9909632d0e116ea07720636a03
cites cdi_FETCH-LOGICAL-c512t-4a770930c2bf774dff6d33c6850e43804b5d8dd9909632d0e116ea07720636a03
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container_title International journal of cardiology
container_volume 149
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&amp;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. 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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.</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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ispartof International journal of cardiology, 2011-06, Vol.149 (2), p.221-226
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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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