Please use this identifier to cite or link to this item: https://doi.org/10.1007/s12195-011-0193-8
DC FieldValue
dc.titleCollective migration behaviors of human breast cancer cells in 2D
dc.contributor.authorMendoz, E.
dc.contributor.authorLim, C.T.
dc.date.accessioned2014-06-17T09:42:52Z
dc.date.available2014-06-17T09:42:52Z
dc.date.issued2011-09
dc.identifier.citationMendoz, E., Lim, C.T. (2011-09). Collective migration behaviors of human breast cancer cells in 2D. Cellular and Molecular Bioengineering 4 (3) : 411-426. ScholarBank@NUS Repository. https://doi.org/10.1007/s12195-011-0193-8
dc.identifier.issn18655025
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/66970
dc.description.abstractCancer related deaths are mainly attributed to the spread of cancer cells to distant organs to form secondary tumors by a process called metastasis. Migration is one of the factors among many others that are strongly implicated in this phenomenon. Here we studied the migratory behavior of benign (MCF-10A), non-invasive malignant (MCF-7) and highly-invasive malignant (MDA-MB-231) tumor cell lines which are derivatives of ductal epithelium of the human breast, using a modified ring cell migration assay technique. Time lapse phase contrast video microscopy was used to monitor migration on both culture coated and Collagen-IV coated surfaces. Individual cells were tracked for 24 h and observations were made on the morphological development of the lamellipods. Analyses show that an intact intercellular adhesion coupled with unidirectional lamellipod formation in benign cells help to coordinate migratory behavior when compared against the malignant variants. Among the cancer cell lines, the non-invasive malignant cells had shorter migratory distances and exhibited pseudo-coordinated behavior due to altered or defective lamellipod morphology and intercellular adhesion, while the highly invasive malignant cells displayed individualistic and chaotic movements with little or no intercellular adhesion. Collagen-IV coating increased the migration rates of the highly invasive cell lines, while the effect was less pronounced on the other two cell lines. © 2011 Biomedical Engineering Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1007/s12195-011-0193-8
dc.sourceScopus
dc.subject2D collective cell migration
dc.subjectCancer metastasis
dc.subjectCell mechanics
dc.subjectCell-cell adhesion
dc.subjectLamellipod formation
dc.typeArticle
dc.contributor.departmentBIOENGINEERING
dc.description.doi10.1007/s12195-011-0193-8
dc.description.sourcetitleCellular and Molecular Bioengineering
dc.description.volume4
dc.description.issue3
dc.description.page411-426
dc.identifier.isiut000297866300010
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