2D protrusion but not motility predicts growth factor-induced cancer cell migration in 3D collagen
Growth factor-induced migration is a critical step in the dissemination and metastasis of solid tumors. Although differences in properties characterizing cell migration on two-dimensional (2D) substrata versus within three-dimensional (3D) matrices have been noted for particular growth factor stimul...
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Veröffentlicht in: | The Journal of cell biology 2012-06, Vol.197 (6), p.721-729 |
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creator | Meyer, Aaron S Hughes-Alford, Shannon K Kay, Jennifer E Castillo, Amalchi Wells, Alan Gertler, Frank B Lauffenburger, Douglas A |
description | Growth factor-induced migration is a critical step in the dissemination and metastasis of solid tumors. Although differences in properties characterizing cell migration on two-dimensional (2D) substrata versus within three-dimensional (3D) matrices have been noted for particular growth factor stimuli, the 2D approach remains in more common use as an efficient surrogate, especially for high-throughput experiments. We therefore were motivated to investigate which migration properties measured in various 2D assays might be reflective of 3D migratory behavioral responses. We used human triple-negative breast cancer lines stimulated by a panel of receptor tyrosine kinase ligands relevant to mammary carcinoma progression. Whereas 2D migration properties did not correlate well with 3D behavior across multiple growth factors, we found that increased membrane protrusion elicited by growth factor stimulation did relate robustly to enhanced 3D migration properties of the MDA-MB-231 and MDA-MB-157 lines. Interestingly, we observed this to be a more reliable relationship than cognate receptor expression or activation levels across these and two additional mammary tumor lines. |
doi_str_mv | 10.1083/jcb.201201003 |
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Although differences in properties characterizing cell migration on two-dimensional (2D) substrata versus within three-dimensional (3D) matrices have been noted for particular growth factor stimuli, the 2D approach remains in more common use as an efficient surrogate, especially for high-throughput experiments. We therefore were motivated to investigate which migration properties measured in various 2D assays might be reflective of 3D migratory behavioral responses. We used human triple-negative breast cancer lines stimulated by a panel of receptor tyrosine kinase ligands relevant to mammary carcinoma progression. Whereas 2D migration properties did not correlate well with 3D behavior across multiple growth factors, we found that increased membrane protrusion elicited by growth factor stimulation did relate robustly to enhanced 3D migration properties of the MDA-MB-231 and MDA-MB-157 lines. Interestingly, we observed this to be a more reliable relationship than cognate receptor expression or activation levels across these and two additional mammary tumor lines.</description><identifier>ISSN: 0021-9525</identifier><identifier>EISSN: 1540-8140</identifier><identifier>DOI: 10.1083/jcb.201201003</identifier><identifier>PMID: 22665521</identifier><identifier>CODEN: JCLBA3</identifier><language>eng</language><publisher>United States: Rockefeller University Press</publisher><subject>Animals ; Breast Neoplasms - metabolism ; Breast Neoplasms - pathology ; Cancer ; Cell adhesion & migration ; Cell Line, Tumor ; Cell Movement ; Cell Proliferation ; Collagen ; Collagen - metabolism ; Female ; Humans ; Intercellular Signaling Peptides and Proteins - metabolism ; Ligands ; Metastasis ; Neoplasms - metabolism ; Neoplasms - pathology ; Receptor Protein-Tyrosine Kinases - metabolism ; Tumors</subject><ispartof>The Journal of cell biology, 2012-06, Vol.197 (6), p.721-729</ispartof><rights>Copyright Rockefeller University Press Jun 11, 2012</rights><rights>2012 Meyer et al. 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c415t-42b8b7746846b60d46b34d668c6b2927622579d11b94cbeca5174e1486c1c3423</citedby><cites>FETCH-LOGICAL-c415t-42b8b7746846b60d46b34d668c6b2927622579d11b94cbeca5174e1486c1c3423</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/22665521$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Meyer, Aaron S</creatorcontrib><creatorcontrib>Hughes-Alford, Shannon K</creatorcontrib><creatorcontrib>Kay, Jennifer E</creatorcontrib><creatorcontrib>Castillo, Amalchi</creatorcontrib><creatorcontrib>Wells, Alan</creatorcontrib><creatorcontrib>Gertler, Frank B</creatorcontrib><creatorcontrib>Lauffenburger, Douglas A</creatorcontrib><title>2D protrusion but not motility predicts growth factor-induced cancer cell migration in 3D collagen</title><title>The Journal of cell biology</title><addtitle>J Cell Biol</addtitle><description>Growth factor-induced migration is a critical step in the dissemination and metastasis of solid tumors. Although differences in properties characterizing cell migration on two-dimensional (2D) substrata versus within three-dimensional (3D) matrices have been noted for particular growth factor stimuli, the 2D approach remains in more common use as an efficient surrogate, especially for high-throughput experiments. We therefore were motivated to investigate which migration properties measured in various 2D assays might be reflective of 3D migratory behavioral responses. We used human triple-negative breast cancer lines stimulated by a panel of receptor tyrosine kinase ligands relevant to mammary carcinoma progression. Whereas 2D migration properties did not correlate well with 3D behavior across multiple growth factors, we found that increased membrane protrusion elicited by growth factor stimulation did relate robustly to enhanced 3D migration properties of the MDA-MB-231 and MDA-MB-157 lines. Interestingly, we observed this to be a more reliable relationship than cognate receptor expression or activation levels across these and two additional mammary tumor lines.</description><subject>Animals</subject><subject>Breast Neoplasms - metabolism</subject><subject>Breast Neoplasms - pathology</subject><subject>Cancer</subject><subject>Cell adhesion & migration</subject><subject>Cell Line, Tumor</subject><subject>Cell Movement</subject><subject>Cell Proliferation</subject><subject>Collagen</subject><subject>Collagen - metabolism</subject><subject>Female</subject><subject>Humans</subject><subject>Intercellular Signaling Peptides and Proteins - metabolism</subject><subject>Ligands</subject><subject>Metastasis</subject><subject>Neoplasms - metabolism</subject><subject>Neoplasms - pathology</subject><subject>Receptor Protein-Tyrosine Kinases - metabolism</subject><subject>Tumors</subject><issn>0021-9525</issn><issn>1540-8140</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkc1rHCEYh6WkNNu0x1yDkEsvk_r6OXMJlKRfEOilPYs67sZlRjfqJOS_j9ukS1sQPbwPD_7eH0KnQC6A9Ozj1tkLSqAdQtgrtALBSdcDJ0doRQiFbhBUHKO3pWwJIVxx9gYdUyqlEBRWyNJrvMup5qWEFLFdKo6p4jnVMIX62GZ-DK4WvMnpod7itXE15S7EcXF-xM5E5zN2fprwHDbZ1L0lRMyusUvTZDY-vkOv12Yq_v3Le4J-ffn88-pbd_Pj6_erTzed4yBqx6ntrVJc9lxaScZ2Mz5K2Ttp6UCVpFSoYQSwA3fWOyNAcQ-8lw4c45SdoMtn726xsx-djzWbSe9ymE1-1MkE_e8khlu9SfeaMcU4kCb48CLI6W7xpeo5lH00E31aigbSttyrQciGnv-HbtOSY4u3p4AJpn4Lu2fK5VRK9uvDZ4DofXu6tacP7TX-7O8EB_pPXewJK66VDQ</recordid><startdate>20120611</startdate><enddate>20120611</enddate><creator>Meyer, Aaron S</creator><creator>Hughes-Alford, Shannon K</creator><creator>Kay, Jennifer E</creator><creator>Castillo, Amalchi</creator><creator>Wells, Alan</creator><creator>Gertler, Frank B</creator><creator>Lauffenburger, Douglas A</creator><general>Rockefeller University Press</general><general>The Rockefeller University Press</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>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20120611</creationdate><title>2D protrusion but not motility predicts growth factor-induced cancer cell migration in 3D collagen</title><author>Meyer, Aaron S ; Hughes-Alford, Shannon K ; Kay, Jennifer E ; Castillo, Amalchi ; Wells, Alan ; Gertler, Frank B ; Lauffenburger, Douglas A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c415t-42b8b7746846b60d46b34d668c6b2927622579d11b94cbeca5174e1486c1c3423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Breast Neoplasms - metabolism</topic><topic>Breast Neoplasms - pathology</topic><topic>Cancer</topic><topic>Cell adhesion & migration</topic><topic>Cell Line, Tumor</topic><topic>Cell Movement</topic><topic>Cell Proliferation</topic><topic>Collagen</topic><topic>Collagen - metabolism</topic><topic>Female</topic><topic>Humans</topic><topic>Intercellular Signaling Peptides and Proteins - metabolism</topic><topic>Ligands</topic><topic>Metastasis</topic><topic>Neoplasms - metabolism</topic><topic>Neoplasms - pathology</topic><topic>Receptor Protein-Tyrosine Kinases - metabolism</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Meyer, Aaron S</creatorcontrib><creatorcontrib>Hughes-Alford, Shannon K</creatorcontrib><creatorcontrib>Kay, Jennifer E</creatorcontrib><creatorcontrib>Castillo, Amalchi</creatorcontrib><creatorcontrib>Wells, Alan</creatorcontrib><creatorcontrib>Gertler, Frank B</creatorcontrib><creatorcontrib>Lauffenburger, Douglas A</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Meyer, Aaron S</au><au>Hughes-Alford, Shannon K</au><au>Kay, Jennifer E</au><au>Castillo, Amalchi</au><au>Wells, Alan</au><au>Gertler, Frank B</au><au>Lauffenburger, Douglas A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>2D protrusion but not motility predicts growth factor-induced cancer cell migration in 3D collagen</atitle><jtitle>The Journal of cell biology</jtitle><addtitle>J Cell Biol</addtitle><date>2012-06-11</date><risdate>2012</risdate><volume>197</volume><issue>6</issue><spage>721</spage><epage>729</epage><pages>721-729</pages><issn>0021-9525</issn><eissn>1540-8140</eissn><coden>JCLBA3</coden><abstract>Growth factor-induced migration is a critical step in the dissemination and metastasis of solid tumors. Although differences in properties characterizing cell migration on two-dimensional (2D) substrata versus within three-dimensional (3D) matrices have been noted for particular growth factor stimuli, the 2D approach remains in more common use as an efficient surrogate, especially for high-throughput experiments. We therefore were motivated to investigate which migration properties measured in various 2D assays might be reflective of 3D migratory behavioral responses. We used human triple-negative breast cancer lines stimulated by a panel of receptor tyrosine kinase ligands relevant to mammary carcinoma progression. Whereas 2D migration properties did not correlate well with 3D behavior across multiple growth factors, we found that increased membrane protrusion elicited by growth factor stimulation did relate robustly to enhanced 3D migration properties of the MDA-MB-231 and MDA-MB-157 lines. 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subjects | Animals Breast Neoplasms - metabolism Breast Neoplasms - pathology Cancer Cell adhesion & migration Cell Line, Tumor Cell Movement Cell Proliferation Collagen Collagen - metabolism Female Humans Intercellular Signaling Peptides and Proteins - metabolism Ligands Metastasis Neoplasms - metabolism Neoplasms - pathology Receptor Protein-Tyrosine Kinases - metabolism Tumors |
title | 2D protrusion but not motility predicts growth factor-induced cancer cell migration in 3D collagen |
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