Show simple item record

dc.contributor.authorMeyer, Aaron Samuel
dc.contributor.authorHughes-Alford, Shannon Kay
dc.contributor.authorKay, Jennifer Elizabeth
dc.contributor.authorCastillo, Amalchi
dc.contributor.authorWells, Alan
dc.contributor.authorGertler, Frank
dc.contributor.authorLauffenburger, Douglas A
dc.date.accessioned2012-07-27T14:45:36Z
dc.date.available2012-07-27T14:45:36Z
dc.date.issued2012-06
dc.date.submitted2012-01
dc.identifier.issn0021-9525
dc.identifier.issn1540-8140
dc.identifier.urihttp://hdl.handle.net/1721.1/71869
dc.description.abstractGrowth 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.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant no. R01- GM081336)en_US
dc.description.sponsorshipNational Science Foundation (U.S.). Graduate Research Fellowshipen_US
dc.description.sponsorshipUnited States. Dept. of Defense. Congressionally Directed Medical Research Programs. Breast Cancer Research Program (Grant no. W81XWH-11-1-0088)en_US
dc.description.sponsorshipUnited States. Dept. of Defense. Congressionally Directed Medical Research Programs. Breast Cancer Research Program (Grant no. W81XWH-10-1-0040)en_US
dc.language.isoen_US
dc.publisherRockefeller University Press, Theen_US
dc.relation.isversionofhttp://dx.doi.org/10.1083/jcb.201201003en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0 Unporteden_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourceRockefeller UPen_US
dc.title2D protrusion but not motility predicts growth factor–induced cancer cell migration in 3D collagenen_US
dc.typeArticleen_US
dc.identifier.citationMeyer, A. S. et al. “2D Protrusion but Not Motility Predicts Growth Factor-induced Cancer Cell Migration in 3D Collagen.” The Journal of Cell Biology 197.6 (2012): 721–729. Copyright © 2012 by The Rockefeller University Pressen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.approverLauffenburger, Douglas A.
dc.contributor.mitauthorMeyer, Aaron Samuel
dc.contributor.mitauthorHughes-Alford, Shannon Kay
dc.contributor.mitauthorKay, Jennifer Elizabeth
dc.contributor.mitauthorCastillo, Amalchi
dc.contributor.mitauthorGertler, Frank
dc.contributor.mitauthorLauffenburger, Douglas A.
dc.relation.journalJournal of Cell Biologyen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsMeyer, A. S.; Hughes-Alford, S. K.; Kay, J. E.; Castillo, A.; Wells, A.; Gertler, F. B.; Lauffenburger, D. A.en
dc.identifier.orcidhttps://orcid.org/0000-0001-5891-0689
dc.identifier.orcidhttps://orcid.org/0000-0003-3214-4554
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record