Cell Adhesion Molecules in Cardiovascular Pathology – A Glance into the Future?

Increasing evidence shows that atherosclerosis is a low-grade chronic inflammatory disease. The interaction between the arterial wall and circulating blood cells like monocytes and T lymphocytes is an important step in this inflammatory process. This interaction is mediated via transmembrane glycopr...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Heart drug 2001, Vol.1 (4), p.225-235
Hauptverfasser: Goudev, Assen, Georgiev, Dimiter, Atar, Dan, Kehayov, Ivan, Kyurkchiev, Stanimir
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 235
container_issue 4
container_start_page 225
container_title Heart drug
container_volume 1
creator Goudev, Assen
Georgiev, Dimiter
Atar, Dan
Kehayov, Ivan
Kyurkchiev, Stanimir
description Increasing evidence shows that atherosclerosis is a low-grade chronic inflammatory disease. The interaction between the arterial wall and circulating blood cells like monocytes and T lymphocytes is an important step in this inflammatory process. This interaction is mediated via transmembrane glycoprotein receptors known as cellular adhesion molecules (CAM). The expression of these molecules is provoked by a variety of cardiovascular risk factors and is under the control notably of inflammatory cytokines, hemodynamic factors, bacterial endotoxins. Recently, data from large prospective studies have shown that an increased concentration of CAM predicts an increased cardiovascular risk. There is an increasing interest in CAM as a new therapeutic target in atherosclerosis.
doi_str_mv 10.1159/000048964
format Article
fullrecord <record><control><sourceid>karger_cross</sourceid><recordid>TN_cdi_karger_primary_48964</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>48964</sourcerecordid><originalsourceid>FETCH-LOGICAL-c189t-430cd2687c8aad39fd8894a4632cba9a777f45a7ce0839848d014ddc28af488f3</originalsourceid><addsrcrecordid>eNpt0L9OwzAQBnALgUQFHZhZLDaGgB07yXlCVegfpCJAgjm62k4bYerKTpG68Q68IU9C2qJO3HKn00_f8BFywdkN55m6Zd1IULk8Ij0uU5mwLMuPd3eaqCyFU9KPsZmxTAhQqmA98lJa5-jALGxs_JI-emf12tlImyUtMZjGf2LsPhjoM7YL7_x8Q3--vumAjh0ute1g62m7sHS0btfB3p2TkxpdtP2_fUbeRsPXcpJMn8YP5WCaaA6qTaRg2qQ5FBoQjVC1AVASZS5SPUOFRVHUMsNCWwZCgQTDuDRGp4C1BKjFGbne5-rgYwy2rlah-cCwqTirtnVUhzo6e7W37xjmNhzkZHi_A9XKbAMv_0X7iF83sGbo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Cell Adhesion Molecules in Cardiovascular Pathology – A Glance into the Future?</title><source>Karger Journals</source><creator>Goudev, Assen ; Georgiev, Dimiter ; Atar, Dan ; Kehayov, Ivan ; Kyurkchiev, Stanimir</creator><creatorcontrib>Goudev, Assen ; Georgiev, Dimiter ; Atar, Dan ; Kehayov, Ivan ; Kyurkchiev, Stanimir</creatorcontrib><description>Increasing evidence shows that atherosclerosis is a low-grade chronic inflammatory disease. The interaction between the arterial wall and circulating blood cells like monocytes and T lymphocytes is an important step in this inflammatory process. This interaction is mediated via transmembrane glycoprotein receptors known as cellular adhesion molecules (CAM). The expression of these molecules is provoked by a variety of cardiovascular risk factors and is under the control notably of inflammatory cytokines, hemodynamic factors, bacterial endotoxins. Recently, data from large prospective studies have shown that an increased concentration of CAM predicts an increased cardiovascular risk. There is an increasing interest in CAM as a new therapeutic target in atherosclerosis.</description><identifier>ISSN: 1422-9528</identifier><identifier>EISSN: 1424-0556</identifier><identifier>DOI: 10.1159/000048964</identifier><language>eng</language><publisher>Basel, Switzerland</publisher><subject>Review</subject><ispartof>Heart drug, 2001, Vol.1 (4), p.225-235</ispartof><rights>2001 S. Karger AG, Basel</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c189t-430cd2687c8aad39fd8894a4632cba9a777f45a7ce0839848d014ddc28af488f3</citedby><cites>FETCH-LOGICAL-c189t-430cd2687c8aad39fd8894a4632cba9a777f45a7ce0839848d014ddc28af488f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,2430,4025,27928,27929,27930</link.rule.ids></links><search><creatorcontrib>Goudev, Assen</creatorcontrib><creatorcontrib>Georgiev, Dimiter</creatorcontrib><creatorcontrib>Atar, Dan</creatorcontrib><creatorcontrib>Kehayov, Ivan</creatorcontrib><creatorcontrib>Kyurkchiev, Stanimir</creatorcontrib><title>Cell Adhesion Molecules in Cardiovascular Pathology – A Glance into the Future?</title><title>Heart drug</title><addtitle>Heart Drug</addtitle><description>Increasing evidence shows that atherosclerosis is a low-grade chronic inflammatory disease. The interaction between the arterial wall and circulating blood cells like monocytes and T lymphocytes is an important step in this inflammatory process. This interaction is mediated via transmembrane glycoprotein receptors known as cellular adhesion molecules (CAM). The expression of these molecules is provoked by a variety of cardiovascular risk factors and is under the control notably of inflammatory cytokines, hemodynamic factors, bacterial endotoxins. Recently, data from large prospective studies have shown that an increased concentration of CAM predicts an increased cardiovascular risk. There is an increasing interest in CAM as a new therapeutic target in atherosclerosis.</description><subject>Review</subject><issn>1422-9528</issn><issn>1424-0556</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNpt0L9OwzAQBnALgUQFHZhZLDaGgB07yXlCVegfpCJAgjm62k4bYerKTpG68Q68IU9C2qJO3HKn00_f8BFywdkN55m6Zd1IULk8Ij0uU5mwLMuPd3eaqCyFU9KPsZmxTAhQqmA98lJa5-jALGxs_JI-emf12tlImyUtMZjGf2LsPhjoM7YL7_x8Q3--vumAjh0ute1g62m7sHS0btfB3p2TkxpdtP2_fUbeRsPXcpJMn8YP5WCaaA6qTaRg2qQ5FBoQjVC1AVASZS5SPUOFRVHUMsNCWwZCgQTDuDRGp4C1BKjFGbne5-rgYwy2rlah-cCwqTirtnVUhzo6e7W37xjmNhzkZHi_A9XKbAMv_0X7iF83sGbo</recordid><startdate>2001</startdate><enddate>2001</enddate><creator>Goudev, Assen</creator><creator>Georgiev, Dimiter</creator><creator>Atar, Dan</creator><creator>Kehayov, Ivan</creator><creator>Kyurkchiev, Stanimir</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>2001</creationdate><title>Cell Adhesion Molecules in Cardiovascular Pathology – A Glance into the Future?</title><author>Goudev, Assen ; Georgiev, Dimiter ; Atar, Dan ; Kehayov, Ivan ; Kyurkchiev, Stanimir</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c189t-430cd2687c8aad39fd8894a4632cba9a777f45a7ce0839848d014ddc28af488f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Review</topic><toplevel>online_resources</toplevel><creatorcontrib>Goudev, Assen</creatorcontrib><creatorcontrib>Georgiev, Dimiter</creatorcontrib><creatorcontrib>Atar, Dan</creatorcontrib><creatorcontrib>Kehayov, Ivan</creatorcontrib><creatorcontrib>Kyurkchiev, Stanimir</creatorcontrib><collection>CrossRef</collection><jtitle>Heart drug</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Goudev, Assen</au><au>Georgiev, Dimiter</au><au>Atar, Dan</au><au>Kehayov, Ivan</au><au>Kyurkchiev, Stanimir</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cell Adhesion Molecules in Cardiovascular Pathology – A Glance into the Future?</atitle><jtitle>Heart drug</jtitle><addtitle>Heart Drug</addtitle><date>2001</date><risdate>2001</risdate><volume>1</volume><issue>4</issue><spage>225</spage><epage>235</epage><pages>225-235</pages><issn>1422-9528</issn><eissn>1424-0556</eissn><abstract>Increasing evidence shows that atherosclerosis is a low-grade chronic inflammatory disease. The interaction between the arterial wall and circulating blood cells like monocytes and T lymphocytes is an important step in this inflammatory process. This interaction is mediated via transmembrane glycoprotein receptors known as cellular adhesion molecules (CAM). The expression of these molecules is provoked by a variety of cardiovascular risk factors and is under the control notably of inflammatory cytokines, hemodynamic factors, bacterial endotoxins. Recently, data from large prospective studies have shown that an increased concentration of CAM predicts an increased cardiovascular risk. There is an increasing interest in CAM as a new therapeutic target in atherosclerosis.</abstract><cop>Basel, Switzerland</cop><doi>10.1159/000048964</doi><tpages>11</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1422-9528
ispartof Heart drug, 2001, Vol.1 (4), p.225-235
issn 1422-9528
1424-0556
language eng
recordid cdi_karger_primary_48964
source Karger Journals
subjects Review
title Cell Adhesion Molecules in Cardiovascular Pathology – A Glance into the Future?
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-13T10%3A04%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-karger_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cell%20Adhesion%20Molecules%20in%20Cardiovascular%20Pathology%20%E2%80%93%20A%20Glance%20into%20the%20Future?&rft.jtitle=Heart%20drug&rft.au=Goudev,%20Assen&rft.date=2001&rft.volume=1&rft.issue=4&rft.spage=225&rft.epage=235&rft.pages=225-235&rft.issn=1422-9528&rft.eissn=1424-0556&rft_id=info:doi/10.1159/000048964&rft_dat=%3Ckarger_cross%3E48964%3C/karger_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true