Differential expression and biological activity of the heparin‐binding growth‐associated molecule (HB‐GAM) in lung cancer cell lines
The growth of human lung cancer cells is regulated positively and negatively by a variety of growth factors through autocrine as well as paracrine mechanisms. In the present report, we studied the differential role and expression of a neuropolypeptide growth factor in 26 lung cancer cell lines. Expr...
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Veröffentlicht in: | International journal of cancer 1997-11, Vol.73 (4), p.537-543 |
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container_title | International journal of cancer |
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creator | Jäger, Robert Noll, Katja Havemann, Klaus Pflüger, Karl‐H. Knabbe, Cornelius Rauvala, Heikki Zugmaier, Gerhard |
description | The growth of human lung cancer cells is regulated positively and negatively by a variety of growth factors through autocrine as well as paracrine mechanisms. In the present report, we studied the differential role and expression of a neuropolypeptide growth factor in 26 lung cancer cell lines. Expression of the heparin‐binding growth‐associated molecule (HB‐GAM) in 12 small cell lung cancer (SCLC) cell lines was compared to that in 14 non‐small cell lung cancer (NSCLC) cell lines. HB‐GAM mRNA was expressed in 9 of 12 SCLC and 3 of 14 NSCLC cell lines as determined by RT‐PCR analyses. Normal human bronchial epithelial cells were used as negative controls. All cell lines which expressed HB‐GAM mRNA produced HB‐GAM protein as well. Western blot analysis showed that the tumor cells secreted HB‐GAM into the media. HB‐GAM, purified from lung cancer cell lines, exerted biological activity on fibroblasts, endothelial cells and SW13 cells as determined by thymidine incorporation and soft agar cloning assays. In addition, the biological activity of HB‐GAM was blocked by a specific antibody in a dose‐dependent way. Our findings suggest that HB‐GAM may serve as a marker for SCLC cell lines and that it may function as a paracrine growth factor in human lung cancer. HB‐GAM may be a further member of the network of growth factors involved in proliferation, angiogenesis and metastasis of lung tumors. Int. J. Cancer 73:537–543, 1997. © 1997 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/(SICI)1097-0215(19971114)73:4<537::AID-IJC14>3.0.CO;2-6 |
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In the present report, we studied the differential role and expression of a neuropolypeptide growth factor in 26 lung cancer cell lines. Expression of the heparin‐binding growth‐associated molecule (HB‐GAM) in 12 small cell lung cancer (SCLC) cell lines was compared to that in 14 non‐small cell lung cancer (NSCLC) cell lines. HB‐GAM mRNA was expressed in 9 of 12 SCLC and 3 of 14 NSCLC cell lines as determined by RT‐PCR analyses. Normal human bronchial epithelial cells were used as negative controls. All cell lines which expressed HB‐GAM mRNA produced HB‐GAM protein as well. Western blot analysis showed that the tumor cells secreted HB‐GAM into the media. HB‐GAM, purified from lung cancer cell lines, exerted biological activity on fibroblasts, endothelial cells and SW13 cells as determined by thymidine incorporation and soft agar cloning assays. In addition, the biological activity of HB‐GAM was blocked by a specific antibody in a dose‐dependent way. Our findings suggest that HB‐GAM may serve as a marker for SCLC cell lines and that it may function as a paracrine growth factor in human lung cancer. HB‐GAM may be a further member of the network of growth factors involved in proliferation, angiogenesis and metastasis of lung tumors. Int. J. Cancer 73:537–543, 1997. © 1997 Wiley‐Liss, Inc.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/(SICI)1097-0215(19971114)73:4<537::AID-IJC14>3.0.CO;2-6</identifier><identifier>PMID: 9389569</identifier><identifier>CODEN: IJCNAW</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Biological and medical sciences ; Blotting, Western ; Carcinoma, Small Cell - metabolism ; Carcinoma, Small Cell - pathology ; Carrier Proteins - genetics ; Carrier Proteins - isolation & purification ; Carrier Proteins - metabolism ; Cytokines - genetics ; Cytokines - isolation & purification ; Cytokines - metabolism ; Growth Substances - genetics ; Growth Substances - isolation & purification ; Growth Substances - metabolism ; Humans ; Lung Neoplasms - metabolism ; Lung Neoplasms - pathology ; Medical sciences ; Neoplasm Proteins - genetics ; Neoplasm Proteins - isolation & purification ; Neoplasm Proteins - metabolism ; Pneumology ; RNA, Messenger - metabolism ; Tumor Cells, Cultured ; Tumor Stem Cell Assay ; Tumors of the respiratory system and mediastinum</subject><ispartof>International journal of cancer, 1997-11, Vol.73 (4), p.537-543</ispartof><rights>Copyright © 1997 Wiley‐Liss, Inc.</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4274-8edf9d268c60e34cd737719b9e3ff810789ff635429c7bb6d61e8a0516bc655f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2F%28SICI%291097-0215%2819971114%2973%3A4%3C537%3A%3AAID-IJC14%3E3.0.CO%3B2-6$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2F%28SICI%291097-0215%2819971114%2973%3A4%3C537%3A%3AAID-IJC14%3E3.0.CO%3B2-6$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2073898$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9389569$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jäger, Robert</creatorcontrib><creatorcontrib>Noll, Katja</creatorcontrib><creatorcontrib>Havemann, Klaus</creatorcontrib><creatorcontrib>Pflüger, Karl‐H.</creatorcontrib><creatorcontrib>Knabbe, Cornelius</creatorcontrib><creatorcontrib>Rauvala, Heikki</creatorcontrib><creatorcontrib>Zugmaier, Gerhard</creatorcontrib><title>Differential expression and biological activity of the heparin‐binding growth‐associated molecule (HB‐GAM) in lung cancer cell lines</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>The growth of human lung cancer cells is regulated positively and negatively by a variety of growth factors through autocrine as well as paracrine mechanisms. In the present report, we studied the differential role and expression of a neuropolypeptide growth factor in 26 lung cancer cell lines. Expression of the heparin‐binding growth‐associated molecule (HB‐GAM) in 12 small cell lung cancer (SCLC) cell lines was compared to that in 14 non‐small cell lung cancer (NSCLC) cell lines. HB‐GAM mRNA was expressed in 9 of 12 SCLC and 3 of 14 NSCLC cell lines as determined by RT‐PCR analyses. Normal human bronchial epithelial cells were used as negative controls. All cell lines which expressed HB‐GAM mRNA produced HB‐GAM protein as well. Western blot analysis showed that the tumor cells secreted HB‐GAM into the media. HB‐GAM, purified from lung cancer cell lines, exerted biological activity on fibroblasts, endothelial cells and SW13 cells as determined by thymidine incorporation and soft agar cloning assays. In addition, the biological activity of HB‐GAM was blocked by a specific antibody in a dose‐dependent way. Our findings suggest that HB‐GAM may serve as a marker for SCLC cell lines and that it may function as a paracrine growth factor in human lung cancer. HB‐GAM may be a further member of the network of growth factors involved in proliferation, angiogenesis and metastasis of lung tumors. Int. J. Cancer 73:537–543, 1997. © 1997 Wiley‐Liss, Inc.</description><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Carcinoma, Small Cell - metabolism</subject><subject>Carcinoma, Small Cell - pathology</subject><subject>Carrier Proteins - genetics</subject><subject>Carrier Proteins - isolation & purification</subject><subject>Carrier Proteins - metabolism</subject><subject>Cytokines - genetics</subject><subject>Cytokines - isolation & purification</subject><subject>Cytokines - metabolism</subject><subject>Growth Substances - genetics</subject><subject>Growth Substances - isolation & purification</subject><subject>Growth Substances - metabolism</subject><subject>Humans</subject><subject>Lung Neoplasms - metabolism</subject><subject>Lung Neoplasms - pathology</subject><subject>Medical sciences</subject><subject>Neoplasm Proteins - genetics</subject><subject>Neoplasm Proteins - isolation & purification</subject><subject>Neoplasm Proteins - metabolism</subject><subject>Pneumology</subject><subject>RNA, Messenger - metabolism</subject><subject>Tumor Cells, Cultured</subject><subject>Tumor Stem Cell Assay</subject><subject>Tumors of the respiratory system and mediastinum</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcGO0zAURSMEGoaBT0DyAqF2kWLHjh0XBCoZmCka1AUg2FmO89wapUmxU4buWLPiG_kSHFq6AWlWlt47vrr2SZIXBE8IxtmT0bt5OR8TLEWKM5KPiJSCEMLGgk7Zs5yK6XQ2P0_nb0rCntMJnpSLp1nKbyWnxzu3k9OYhFNBKL-b3AvhM8aE5JidJCeSFjLn8jT5ce6sBQ9t73SD4NvGQwiua5Fua1S5rumWzsSNNr376vod6izqV4BWsNHetb--_6xcW7t2iZa-u-5XcaBD6IzTPdRo3TVgtg2g0eXLuLmYvR0j16JmG3mjWwMeGWga1LgWwv3kjtVNgAeH8yz58PrV-_IyvVpczMvZVWpYJlhaQG1lnfHCcAyUmVpQIYisJFBrC4JFIa3lNGeZNKKqeM0JFBrnhFeG57mlZ8njfe7Gd1-2EHq1dmGooVvotkEJyWiW58WNIOEZZpjzCH7cg8Z3IXiwauPdWvudIlgNOpUadKpBjRrUqL86laCKqahTqahT_dGpqMKqXKhMDckPDxW21RrqY-7BX9w_Oux1iJqsj5_qwhHLsIjg8JJPe-zaNbD7p92N5f7XbT-gvwGOL8uF</recordid><startdate>19971114</startdate><enddate>19971114</enddate><creator>Jäger, Robert</creator><creator>Noll, Katja</creator><creator>Havemann, Klaus</creator><creator>Pflüger, Karl‐H.</creator><creator>Knabbe, Cornelius</creator><creator>Rauvala, Heikki</creator><creator>Zugmaier, Gerhard</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</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>7TO</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19971114</creationdate><title>Differential expression and biological activity of the heparin‐binding growth‐associated molecule (HB‐GAM) in lung cancer cell lines</title><author>Jäger, Robert ; Noll, Katja ; Havemann, Klaus ; Pflüger, Karl‐H. ; Knabbe, Cornelius ; Rauvala, Heikki ; Zugmaier, Gerhard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4274-8edf9d268c60e34cd737719b9e3ff810789ff635429c7bb6d61e8a0516bc655f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Carcinoma, Small Cell - metabolism</topic><topic>Carcinoma, Small Cell - pathology</topic><topic>Carrier Proteins - genetics</topic><topic>Carrier Proteins - isolation & purification</topic><topic>Carrier Proteins - metabolism</topic><topic>Cytokines - genetics</topic><topic>Cytokines - isolation & purification</topic><topic>Cytokines - metabolism</topic><topic>Growth Substances - genetics</topic><topic>Growth Substances - isolation & purification</topic><topic>Growth Substances - metabolism</topic><topic>Humans</topic><topic>Lung Neoplasms - metabolism</topic><topic>Lung Neoplasms - pathology</topic><topic>Medical sciences</topic><topic>Neoplasm Proteins - genetics</topic><topic>Neoplasm Proteins - isolation & purification</topic><topic>Neoplasm Proteins - metabolism</topic><topic>Pneumology</topic><topic>RNA, Messenger - metabolism</topic><topic>Tumor Cells, Cultured</topic><topic>Tumor Stem Cell Assay</topic><topic>Tumors of the respiratory system and mediastinum</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jäger, Robert</creatorcontrib><creatorcontrib>Noll, Katja</creatorcontrib><creatorcontrib>Havemann, Klaus</creatorcontrib><creatorcontrib>Pflüger, Karl‐H.</creatorcontrib><creatorcontrib>Knabbe, Cornelius</creatorcontrib><creatorcontrib>Rauvala, Heikki</creatorcontrib><creatorcontrib>Zugmaier, Gerhard</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>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jäger, Robert</au><au>Noll, Katja</au><au>Havemann, Klaus</au><au>Pflüger, Karl‐H.</au><au>Knabbe, Cornelius</au><au>Rauvala, Heikki</au><au>Zugmaier, Gerhard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential expression and biological activity of the heparin‐binding growth‐associated molecule (HB‐GAM) in lung cancer cell lines</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>1997-11-14</date><risdate>1997</risdate><volume>73</volume><issue>4</issue><spage>537</spage><epage>543</epage><pages>537-543</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><coden>IJCNAW</coden><abstract>The growth of human lung cancer cells is regulated positively and negatively by a variety of growth factors through autocrine as well as paracrine mechanisms. In the present report, we studied the differential role and expression of a neuropolypeptide growth factor in 26 lung cancer cell lines. Expression of the heparin‐binding growth‐associated molecule (HB‐GAM) in 12 small cell lung cancer (SCLC) cell lines was compared to that in 14 non‐small cell lung cancer (NSCLC) cell lines. HB‐GAM mRNA was expressed in 9 of 12 SCLC and 3 of 14 NSCLC cell lines as determined by RT‐PCR analyses. Normal human bronchial epithelial cells were used as negative controls. All cell lines which expressed HB‐GAM mRNA produced HB‐GAM protein as well. Western blot analysis showed that the tumor cells secreted HB‐GAM into the media. HB‐GAM, purified from lung cancer cell lines, exerted biological activity on fibroblasts, endothelial cells and SW13 cells as determined by thymidine incorporation and soft agar cloning assays. In addition, the biological activity of HB‐GAM was blocked by a specific antibody in a dose‐dependent way. Our findings suggest that HB‐GAM may serve as a marker for SCLC cell lines and that it may function as a paracrine growth factor in human lung cancer. HB‐GAM may be a further member of the network of growth factors involved in proliferation, angiogenesis and metastasis of lung tumors. Int. J. Cancer 73:537–543, 1997. © 1997 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>9389569</pmid><doi>10.1002/(SICI)1097-0215(19971114)73:4<537::AID-IJC14>3.0.CO;2-6</doi><tpages>7</tpages></addata></record> |
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subjects | Biological and medical sciences Blotting, Western Carcinoma, Small Cell - metabolism Carcinoma, Small Cell - pathology Carrier Proteins - genetics Carrier Proteins - isolation & purification Carrier Proteins - metabolism Cytokines - genetics Cytokines - isolation & purification Cytokines - metabolism Growth Substances - genetics Growth Substances - isolation & purification Growth Substances - metabolism Humans Lung Neoplasms - metabolism Lung Neoplasms - pathology Medical sciences Neoplasm Proteins - genetics Neoplasm Proteins - isolation & purification Neoplasm Proteins - metabolism Pneumology RNA, Messenger - metabolism Tumor Cells, Cultured Tumor Stem Cell Assay Tumors of the respiratory system and mediastinum |
title | Differential expression and biological activity of the heparin‐binding growth‐associated molecule (HB‐GAM) in lung cancer cell lines |
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