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dc.creatorBaker, Erin L.en
dc.creatorSrivastava, Jayaen
dc.creatorYu, Dihuaen
dc.creatorBonnecaze, Roger T.en
dc.creatorZaman, Muhammad H.en
dc.date.accessioned2013-05-06T16:04:46Zen
dc.date.available2013-05-06T16:04:46Zen
dc.date.issued2011-05-27en
dc.identifier.citationBaker EL, Srivastava J, Yu D, Bonnecaze RT, Zaman MH (2011) Cancer Cell Migration: Integrated Roles of Matrix Mechanics and Transforming Potential. PLoS ONE 6(5): e20355. doi:10.1371/journal.pone.0020355en
dc.identifier.urihttp://hdl.handle.net/2152/20092en
dc.descriptionErin L. Baker is with UT Austin; Jaya Srivastava is with UT Austin; Dihua Yu is with the UT M.D. Anderson Cancer Center; Roger T. Bonnecaze is with UT Austin; Muhammad H. Zaman is with Boston University.en
dc.description.abstractSignificant progress has been achieved toward elucidating the molecular mechanisms that underlie breast cancer progression; yet, much less is known about the associated cellular biophysical traits. To this end, we use time-lapsed confocal microscopy to investigate the interplay among cell motility, three-dimensional (3D) matrix stiffness, matrix architecture, and transforming potential in a mammary epithelial cell (MEC) cancer progression series. We use a well characterized breast cancer progression model where human-derived MCF10A MECs overexpress either ErbB2, 14-3-3ζ, or both ErbB2 and 14-3-3ζ, with empty vector as a control. Cell motility assays showed that MECs overexpressing ErbB2 alone exhibited notably high migration speeds when cultured atop two-dimensional (2D) matrices, while overexpression of 14-3-3ζ alone most suppressed migration atop 2D matrices (as compared to non-transformed MECs). Our results also suggest that co-overexpression of the 14-3-3ζ and ErbB2 proteins facilitates cell migratory capacity in 3D matrices, as reflected in cell migration speed. Additionally, 3D matrices of sufficient stiffness can significantly hinder the migratory ability of partially transformed cells, but increased 3D matrix stiffness has a lesser effect on the aggressive migratory behavior exhibited by fully transformed cells that co-overexpress both ErbB2 and 14-3-3ζ. Finally, this study shows that for MECs possessing partial or full transforming potential, those overexpressing ErbB2 alone show the greatest sensitivity of cell migration speed to matrix architecture, while those overexpressing 14-3-3ζ alone exhibit the least sensitivity to matrix architecture. Given the current knowledge of breast cancer mechanobiology, these findings overall suggest that cell motility is governed by a complex interplay between matrix mechanics and transforming potential.en
dc.description.sponsorshipThis work was made possible by the United Negro College Fund (UNCF)/Merck Graduate Science Research Dissertation Fellowship to ELB, the Philanthropic Educational Organization (P.E.O.) Scholar Award to ELB, the Charles Tate Foundation UT Seed Grant to MHZ and DY, and National Institutes of Health funding (1R01CA132633) to MHZ. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.en
dc.language.isoengen
dc.publisherPublic Library of Scienceen
dc.rightsAttribution 3.0 United Statesen
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/en
dc.subjectBreast canceren
dc.subjectCancer cell migrationen
dc.subjectCell migrationen
dc.subjectCell motilityen
dc.subjectCollagensen
dc.subjectExtracellular matrixen
dc.subjectMembrane potentialen
dc.subjectStiffnessen
dc.titleCancer Cell Migration: Integrated Roles of Matrix Mechanics and Transforming Potentialen
dc.typeArticleen
dc.description.departmentChemical Engineeringen
dc.identifier.doi10.1371/journal.pone.0020355en


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Attribution 3.0 United States
Except where otherwise noted, this item's license is described as Attribution 3.0 United States