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Netrin-4 regulates angiogenic responses and tumor cell growth
Netrin-4 is a 628 amino acid basement membrane component that promotes neurite elongation at low concentrations but inhibits neurite extension at high concentrations. There is a growing body of literature suggesting that several molecules, including netrins, are regulators of both neuronal and vascu...
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Published in: | Experimental cell research 2009-03, Vol.315 (5), p.784-794 |
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description | Netrin-4 is a 628 amino acid basement membrane component that promotes neurite elongation at low concentrations but inhibits neurite extension at high concentrations. There is a growing body of literature suggesting that several molecules, including netrins, are regulators of both neuronal and vascular growth. It is believed that molecules that guide neural growth and development are also involved in regulating morphogenesis of the vascular tree. Further, netrins have recently been implicated in controlling epithelial cell branching morphogenesis in the breast, lung and pancreas.
Characterization of purified netrin-4 in
in vitro angiogenesis assays demonstrated that netrin-4 markedly inhibits HMVEC migration and tube formation. Moreover, netrin-4 inhibits proliferation of a variety of human tumor cells
in vitro. Netrin-4 has only modest effects on proliferation of endothelial and other non-transformed cells. Netrin-4 treatment results in phosphorylation changes of proteins that are known to control cell growth. Specifically, Phospho-Akt-1, Phospho-Jnk-2, and Phospho-c-Jun are reduced in tumor cells that have been treated with netrin-4. Together, these data suggest a potential role for netrin-4 in regulating tumor growth. |
doi_str_mv | 10.1016/j.yexcr.2008.11.018 |
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Characterization of purified netrin-4 in
in vitro angiogenesis assays demonstrated that netrin-4 markedly inhibits HMVEC migration and tube formation. Moreover, netrin-4 inhibits proliferation of a variety of human tumor cells
in vitro. Netrin-4 has only modest effects on proliferation of endothelial and other non-transformed cells. Netrin-4 treatment results in phosphorylation changes of proteins that are known to control cell growth. Specifically, Phospho-Akt-1, Phospho-Jnk-2, and Phospho-c-Jun are reduced in tumor cells that have been treated with netrin-4. Together, these data suggest a potential role for netrin-4 in regulating tumor growth.</description><identifier>ISSN: 0014-4827</identifier><identifier>EISSN: 1090-2422</identifier><identifier>DOI: 10.1016/j.yexcr.2008.11.018</identifier><identifier>PMID: 19094984</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>60 APPLIED LIFE SCIENCES ; Akt ; AMINO ACIDS ; Angiogenesis ; BRANCHING RATIO ; Cell Differentiation - drug effects ; Cell Movement - drug effects ; Cell Movement - genetics ; Cell Proliferation - drug effects ; Cells, Cultured ; Cellular biology ; Dose-Response Relationship, Drug ; Drug Evaluation, Preclinical ; ELONGATION ; Endothelial Cells - drug effects ; Endothelial Cells - physiology ; GROWTH ; Humans ; IN VITRO ; Jnk ; JNK Mitogen-Activated Protein Kinases - antagonists & inhibitors ; LUNGS ; MAMMARY GLANDS ; MOLECULES ; MORPHOGENESIS ; NEOPLASMS ; Neoplasms - blood supply ; Neoplasms - genetics ; Neoplasms - pathology ; Neovascularization, Pathologic - genetics ; Nerve Growth Factors - genetics ; Nerve Growth Factors - pharmacology ; Nerve Growth Factors - physiology ; Netrin-4 ; Netrins ; Oncogene Protein v-akt - antagonists & inhibitors ; PANCREAS ; PHOSPHORYLATION ; Proteins ; RNA, Messenger - metabolism ; Signal Transduction - drug effects ; TUMOR CELLS ; Tumors</subject><ispartof>Experimental cell research, 2009-03, Vol.315 (5), p.784-794</ispartof><rights>2008 Elsevier Inc.</rights><rights>Copyright © 2009 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-b6b5477c13472462000cdb45f482460d839806d24413e221a9f66ac629ef72053</citedby><cites>FETCH-LOGICAL-c478t-b6b5477c13472462000cdb45f482460d839806d24413e221a9f66ac629ef72053</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19094984$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/21176181$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Nacht, Mariana</creatorcontrib><creatorcontrib>St. Martin, Thia B.</creatorcontrib><creatorcontrib>Byrne, Ann</creatorcontrib><creatorcontrib>Klinger, Katherine W.</creatorcontrib><creatorcontrib>Teicher, Beverly A.</creatorcontrib><creatorcontrib>Madden, Stephen L.</creatorcontrib><creatorcontrib>Jiang, Yide</creatorcontrib><title>Netrin-4 regulates angiogenic responses and tumor cell growth</title><title>Experimental cell research</title><addtitle>Exp Cell Res</addtitle><description>Netrin-4 is a 628 amino acid basement membrane component that promotes neurite elongation at low concentrations but inhibits neurite extension at high concentrations. There is a growing body of literature suggesting that several molecules, including netrins, are regulators of both neuronal and vascular growth. It is believed that molecules that guide neural growth and development are also involved in regulating morphogenesis of the vascular tree. Further, netrins have recently been implicated in controlling epithelial cell branching morphogenesis in the breast, lung and pancreas.
Characterization of purified netrin-4 in
in vitro angiogenesis assays demonstrated that netrin-4 markedly inhibits HMVEC migration and tube formation. Moreover, netrin-4 inhibits proliferation of a variety of human tumor cells
in vitro. Netrin-4 has only modest effects on proliferation of endothelial and other non-transformed cells. Netrin-4 treatment results in phosphorylation changes of proteins that are known to control cell growth. Specifically, Phospho-Akt-1, Phospho-Jnk-2, and Phospho-c-Jun are reduced in tumor cells that have been treated with netrin-4. Together, these data suggest a potential role for netrin-4 in regulating tumor growth.</description><subject>60 APPLIED LIFE SCIENCES</subject><subject>Akt</subject><subject>AMINO ACIDS</subject><subject>Angiogenesis</subject><subject>BRANCHING RATIO</subject><subject>Cell Differentiation - drug effects</subject><subject>Cell Movement - drug effects</subject><subject>Cell Movement - genetics</subject><subject>Cell Proliferation - drug effects</subject><subject>Cells, Cultured</subject><subject>Cellular biology</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Evaluation, Preclinical</subject><subject>ELONGATION</subject><subject>Endothelial Cells - drug effects</subject><subject>Endothelial Cells - physiology</subject><subject>GROWTH</subject><subject>Humans</subject><subject>IN VITRO</subject><subject>Jnk</subject><subject>JNK Mitogen-Activated Protein Kinases - antagonists & inhibitors</subject><subject>LUNGS</subject><subject>MAMMARY GLANDS</subject><subject>MOLECULES</subject><subject>MORPHOGENESIS</subject><subject>NEOPLASMS</subject><subject>Neoplasms - blood supply</subject><subject>Neoplasms - genetics</subject><subject>Neoplasms - pathology</subject><subject>Neovascularization, Pathologic - genetics</subject><subject>Nerve Growth Factors - genetics</subject><subject>Nerve Growth Factors - pharmacology</subject><subject>Nerve Growth Factors - physiology</subject><subject>Netrin-4</subject><subject>Netrins</subject><subject>Oncogene Protein v-akt - antagonists & inhibitors</subject><subject>PANCREAS</subject><subject>PHOSPHORYLATION</subject><subject>Proteins</subject><subject>RNA, Messenger - metabolism</subject><subject>Signal Transduction - drug effects</subject><subject>TUMOR CELLS</subject><subject>Tumors</subject><issn>0014-4827</issn><issn>1090-2422</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp9kUFr3DAQhUVI6G63_QWBYhLozY5G1srSIYcQkjYQkkt6Fl55vJHZlbaS3Cb_PnJ2odBDToLhm6f35hFyCrQCCuJiqF7xxYSKUSorgIqCPCJzoIqWjDN2TOaUAi-5ZM2MfI5xoBmUID6RGSiquJJ8Ti4fMAXrSl4EXI-bNmEsWre2fo3OmjyMO-_i-7Ar0rj1oTC42RTr4P-m5y_kpG83Eb8e3gX5dXvzdP2zvH_8cXd9dV8a3shUrsRqyZvGQM0bxkU2TE234ss-e-OCdrJWkoqOcQ41Mgat6oVojWAK-4bRZb0g53tdH5PV0diE5tl459AkzQAaARIy9X1P7YL_PWJMemvj5LZ16MeohVBc1DXP4Nl_4ODH4HICDRkRNVOTWr2HTPAxBuz1LthtG141UD0VoAf9XoCeCtAAOheQt74dpMfVFrt_O4eLZ-ByD2C-1x-LYYqDzmBnw5Sm8_bDD94AGiGUwg</recordid><startdate>20090310</startdate><enddate>20090310</enddate><creator>Nacht, Mariana</creator><creator>St. Martin, Thia B.</creator><creator>Byrne, Ann</creator><creator>Klinger, Katherine W.</creator><creator>Teicher, Beverly A.</creator><creator>Madden, Stephen L.</creator><creator>Jiang, Yide</creator><general>Elsevier Inc</general><general>Elsevier BV</general><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>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>OTOTI</scope></search><sort><creationdate>20090310</creationdate><title>Netrin-4 regulates angiogenic responses and tumor cell growth</title><author>Nacht, Mariana ; St. Martin, Thia B. ; Byrne, Ann ; Klinger, Katherine W. ; Teicher, Beverly A. ; Madden, Stephen L. ; Jiang, Yide</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c478t-b6b5477c13472462000cdb45f482460d839806d24413e221a9f66ac629ef72053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>60 APPLIED LIFE SCIENCES</topic><topic>Akt</topic><topic>AMINO ACIDS</topic><topic>Angiogenesis</topic><topic>BRANCHING RATIO</topic><topic>Cell Differentiation - drug effects</topic><topic>Cell Movement - drug effects</topic><topic>Cell Movement - genetics</topic><topic>Cell Proliferation - drug effects</topic><topic>Cells, Cultured</topic><topic>Cellular biology</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Evaluation, Preclinical</topic><topic>ELONGATION</topic><topic>Endothelial Cells - drug effects</topic><topic>Endothelial Cells - physiology</topic><topic>GROWTH</topic><topic>Humans</topic><topic>IN VITRO</topic><topic>Jnk</topic><topic>JNK Mitogen-Activated Protein Kinases - antagonists & inhibitors</topic><topic>LUNGS</topic><topic>MAMMARY GLANDS</topic><topic>MOLECULES</topic><topic>MORPHOGENESIS</topic><topic>NEOPLASMS</topic><topic>Neoplasms - blood supply</topic><topic>Neoplasms - genetics</topic><topic>Neoplasms - pathology</topic><topic>Neovascularization, Pathologic - genetics</topic><topic>Nerve Growth Factors - genetics</topic><topic>Nerve Growth Factors - pharmacology</topic><topic>Nerve Growth Factors - physiology</topic><topic>Netrin-4</topic><topic>Netrins</topic><topic>Oncogene Protein v-akt - antagonists & inhibitors</topic><topic>PANCREAS</topic><topic>PHOSPHORYLATION</topic><topic>Proteins</topic><topic>RNA, Messenger - metabolism</topic><topic>Signal Transduction - drug effects</topic><topic>TUMOR CELLS</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nacht, Mariana</creatorcontrib><creatorcontrib>St. Martin, Thia B.</creatorcontrib><creatorcontrib>Byrne, Ann</creatorcontrib><creatorcontrib>Klinger, Katherine W.</creatorcontrib><creatorcontrib>Teicher, Beverly A.</creatorcontrib><creatorcontrib>Madden, Stephen L.</creatorcontrib><creatorcontrib>Jiang, Yide</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV</collection><jtitle>Experimental cell research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nacht, Mariana</au><au>St. Martin, Thia B.</au><au>Byrne, Ann</au><au>Klinger, Katherine W.</au><au>Teicher, Beverly A.</au><au>Madden, Stephen L.</au><au>Jiang, Yide</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Netrin-4 regulates angiogenic responses and tumor cell growth</atitle><jtitle>Experimental cell research</jtitle><addtitle>Exp Cell Res</addtitle><date>2009-03-10</date><risdate>2009</risdate><volume>315</volume><issue>5</issue><spage>784</spage><epage>794</epage><pages>784-794</pages><issn>0014-4827</issn><eissn>1090-2422</eissn><abstract>Netrin-4 is a 628 amino acid basement membrane component that promotes neurite elongation at low concentrations but inhibits neurite extension at high concentrations. There is a growing body of literature suggesting that several molecules, including netrins, are regulators of both neuronal and vascular growth. It is believed that molecules that guide neural growth and development are also involved in regulating morphogenesis of the vascular tree. Further, netrins have recently been implicated in controlling epithelial cell branching morphogenesis in the breast, lung and pancreas.
Characterization of purified netrin-4 in
in vitro angiogenesis assays demonstrated that netrin-4 markedly inhibits HMVEC migration and tube formation. Moreover, netrin-4 inhibits proliferation of a variety of human tumor cells
in vitro. Netrin-4 has only modest effects on proliferation of endothelial and other non-transformed cells. Netrin-4 treatment results in phosphorylation changes of proteins that are known to control cell growth. Specifically, Phospho-Akt-1, Phospho-Jnk-2, and Phospho-c-Jun are reduced in tumor cells that have been treated with netrin-4. Together, these data suggest a potential role for netrin-4 in regulating tumor growth.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>19094984</pmid><doi>10.1016/j.yexcr.2008.11.018</doi><tpages>11</tpages></addata></record> |
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subjects | 60 APPLIED LIFE SCIENCES Akt AMINO ACIDS Angiogenesis BRANCHING RATIO Cell Differentiation - drug effects Cell Movement - drug effects Cell Movement - genetics Cell Proliferation - drug effects Cells, Cultured Cellular biology Dose-Response Relationship, Drug Drug Evaluation, Preclinical ELONGATION Endothelial Cells - drug effects Endothelial Cells - physiology GROWTH Humans IN VITRO Jnk JNK Mitogen-Activated Protein Kinases - antagonists & inhibitors LUNGS MAMMARY GLANDS MOLECULES MORPHOGENESIS NEOPLASMS Neoplasms - blood supply Neoplasms - genetics Neoplasms - pathology Neovascularization, Pathologic - genetics Nerve Growth Factors - genetics Nerve Growth Factors - pharmacology Nerve Growth Factors - physiology Netrin-4 Netrins Oncogene Protein v-akt - antagonists & inhibitors PANCREAS PHOSPHORYLATION Proteins RNA, Messenger - metabolism Signal Transduction - drug effects TUMOR CELLS Tumors |
title | Netrin-4 regulates angiogenic responses and tumor cell growth |
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