CXC Chemokines in Angiogenesis Related to Pulmonary Fibrosis
Angiogenesis, defined as the growth of new capillaries from preexisting vessels, is a pervasive biological phenomenon that is at the core of many physiologic and pathologic processes. An opposing balance of angiogenic and angiostatic factors regulates angiogenesis. Examples of physiologic processes...
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Veröffentlicht in: | Chest 2002-12, Vol.122 (6), p.298S-301S |
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description | Angiogenesis, defined as the growth of new capillaries from preexisting vessels, is a pervasive biological phenomenon that is at the core of many physiologic and pathologic processes. An opposing balance of angiogenic and angiostatic factors regulates angiogenesis. Examples of physiologic processes that depend on angiogenesis include embryogenesis, wound repair, and the ovarian/menstrual cycle. In contrast, chronic inflammation associated with chronic fibroproliferative disorders as well as growth and metastasis of solid tumors are associated with aberrant angiogenesis. CXC chemokines comprise a unique cytokine family that contains members that exhibit on a structural/functional basis either angiogenic or angiostatic biological activity. In this review, we will discuss the role of CXC chemokines and angiogenesis in pulmonary fibrosis. |
doi_str_mv | 10.1378/chest.122.6_suppl.298S |
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An opposing balance of angiogenic and angiostatic factors regulates angiogenesis. Examples of physiologic processes that depend on angiogenesis include embryogenesis, wound repair, and the ovarian/menstrual cycle. In contrast, chronic inflammation associated with chronic fibroproliferative disorders as well as growth and metastasis of solid tumors are associated with aberrant angiogenesis. CXC chemokines comprise a unique cytokine family that contains members that exhibit on a structural/functional basis either angiogenic or angiostatic biological activity. 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An opposing balance of angiogenic and angiostatic factors regulates angiogenesis. Examples of physiologic processes that depend on angiogenesis include embryogenesis, wound repair, and the ovarian/menstrual cycle. In contrast, chronic inflammation associated with chronic fibroproliferative disorders as well as growth and metastasis of solid tumors are associated with aberrant angiogenesis. CXC chemokines comprise a unique cytokine family that contains members that exhibit on a structural/functional basis either angiogenic or angiostatic biological activity. In this review, we will discuss the role of CXC chemokines and angiogenesis in pulmonary fibrosis.</description><subject>Amino acids</subject><subject>Angiogenesis</subject><subject>Biological and medical sciences</subject><subject>Blood vessels</subject><subject>Cell cycle</subject><subject>chemokine</subject><subject>Chemokines</subject><subject>Chemokines, CXC - physiology</subject><subject>Chronic obstructive pulmonary disease, asthma</subject><subject>Cytokines</subject><subject>fibrosis</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Interferon</subject><subject>Lung - blood supply</subject><subject>Lung - physiopathology</subject><subject>Medical sciences</subject><subject>Menstruation</subject><subject>Metastasis</subject><subject>Neovascularization, Pathologic - physiopathology</subject><subject>Neutrophils</subject><subject>Ovaries</subject><subject>Pneumology</subject><subject>Proteins</subject><subject>Pulmonary fibrosis</subject><subject>Pulmonary Fibrosis - physiopathology</subject><subject>Receptors, Chemokine - physiology</subject><issn>0012-3692</issn><issn>1931-3543</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkF1rFDEYhYModlv9C2UQ9G7WfGcCXlgGW4WC4gd4FzKZd3ZTM5NtMqP4703dwYIIXoWQc07OeRA6J3hLmGpeuj3keUso3UqTl8MhbKluPj1AG6IZqZng7CHaYExozaSmJ-g05xtc7kTLx-iEUK5Eg_kGvWq_tlW7hzF-8xPkyk_VxbTzcQfl5nP1EYKdoa_mWH1Ywhgnm35Wl75Lsbw-QY8GGzI8Xc8z9OXyzef2bX39_upde3FdOyHwXHeSdc5ySl3HuZZUY0edBUfk4EhnGwwNMCmJVLoTapCCKtULJwc6SMW0ZmfoxTH3kOLtUoab0WcHIdgJ4pKNKgaheVOEz_4S3sQlTaWboRhzzQWjRSSPIldG5ASDOSQ_ll2GYHMH1_yGawpcs8I1d3CL8XxNX7oR-nvbSrMInq8Cm50NQ7KT8_lexzlTsnT402Dvd_sfPoHJow2hxLLj32vrfzR4fTRCof3dQzLZeZgc9CXEzaaP_n8jfgEXlK8x</recordid><startdate>20021201</startdate><enddate>20021201</enddate><creator>Strieter, Robert M.</creator><creator>Belperio, John A.</creator><creator>Keane, Michael P.</creator><general>Elsevier Inc</general><general>American College of Chest Physicians</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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20021201</creationdate><title>CXC Chemokines in Angiogenesis Related to Pulmonary Fibrosis</title><author>Strieter, Robert M. ; Belperio, John A. ; Keane, Michael P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c550t-b63bca422cb4496290c2caec16fc1ba80e8e3661679b57f65277d5c6f2f673993</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Amino acids</topic><topic>Angiogenesis</topic><topic>Biological and medical sciences</topic><topic>Blood vessels</topic><topic>Cell cycle</topic><topic>chemokine</topic><topic>Chemokines</topic><topic>Chemokines, CXC - physiology</topic><topic>Chronic obstructive pulmonary disease, asthma</topic><topic>Cytokines</topic><topic>fibrosis</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Interferon</topic><topic>Lung - blood supply</topic><topic>Lung - physiopathology</topic><topic>Medical sciences</topic><topic>Menstruation</topic><topic>Metastasis</topic><topic>Neovascularization, Pathologic - physiopathology</topic><topic>Neutrophils</topic><topic>Ovaries</topic><topic>Pneumology</topic><topic>Proteins</topic><topic>Pulmonary fibrosis</topic><topic>Pulmonary Fibrosis - physiopathology</topic><topic>Receptors, Chemokine - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Strieter, Robert M.</creatorcontrib><creatorcontrib>Belperio, John A.</creatorcontrib><creatorcontrib>Keane, Michael P.</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>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Chest</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Strieter, Robert M.</au><au>Belperio, John A.</au><au>Keane, Michael P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>CXC Chemokines in Angiogenesis Related to Pulmonary Fibrosis</atitle><jtitle>Chest</jtitle><addtitle>Chest</addtitle><date>2002-12-01</date><risdate>2002</risdate><volume>122</volume><issue>6</issue><spage>298S</spage><epage>301S</epage><pages>298S-301S</pages><issn>0012-3692</issn><eissn>1931-3543</eissn><coden>CHETBF</coden><abstract>Angiogenesis, defined as the growth of new capillaries from preexisting vessels, is a pervasive biological phenomenon that is at the core of many physiologic and pathologic processes. An opposing balance of angiogenic and angiostatic factors regulates angiogenesis. Examples of physiologic processes that depend on angiogenesis include embryogenesis, wound repair, and the ovarian/menstrual cycle. In contrast, chronic inflammation associated with chronic fibroproliferative disorders as well as growth and metastasis of solid tumors are associated with aberrant angiogenesis. CXC chemokines comprise a unique cytokine family that contains members that exhibit on a structural/functional basis either angiogenic or angiostatic biological activity. In this review, we will discuss the role of CXC chemokines and angiogenesis in pulmonary fibrosis.</abstract><cop>Northbrook, IL</cop><pub>Elsevier Inc</pub><pmid>12475804</pmid><doi>10.1378/chest.122.6_suppl.298S</doi></addata></record> |
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subjects | Amino acids Angiogenesis Biological and medical sciences Blood vessels Cell cycle chemokine Chemokines Chemokines, CXC - physiology Chronic obstructive pulmonary disease, asthma Cytokines fibrosis Humans Inflammation Interferon Lung - blood supply Lung - physiopathology Medical sciences Menstruation Metastasis Neovascularization, Pathologic - physiopathology Neutrophils Ovaries Pneumology Proteins Pulmonary fibrosis Pulmonary Fibrosis - physiopathology Receptors, Chemokine - physiology |
title | CXC Chemokines in Angiogenesis Related to Pulmonary Fibrosis |
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