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Attachment, spreading and growth in vitro of highly malignant and low malignant murine fibrosarcoma cells

dc.contributor.authorVarani, Jamesen_US
dc.contributor.authorGrimstad, Ivar Amunden_US
dc.contributor.authorKnibbs, Randall N.en_US
dc.contributor.authorHovig, Torsteinen_US
dc.contributor.authorMcCoy, J. Philip Jr.en_US
dc.date.accessioned2006-09-08T20:30:29Z
dc.date.available2006-09-08T20:30:29Z
dc.date.issued1985-01en_US
dc.identifier.citationVarani, James; Grimstad, Ivar Amund; Knibbs, Randall N.; Hovig, Torstein; McCoy, J. Philip; (1985). "Attachment, spreading and growth in vitro of highly malignant and low malignant murine fibrosarcoma cells." Clinical & Experimental Metastasis 3(1): 45-59. <http://hdl.handle.net/2027.42/42592>en_US
dc.identifier.issn0262-0898en_US
dc.identifier.issn1573-7276en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/42592
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=4042456&dopt=citationen_US
dc.description.abstractHighly malignant cell lines and low-malignant cell lines isolated from three different methylcholanthrene-induced murine fibrosarcomas were examined for their ability to attach to plastic dishes and collagen-coated dishes under serumfree conditions and in the presence of serum. Most of the cells from the three highly malignant lines attached and spread under all conditions. By 72h, there was a significant increase in the number of cells indicating that at least some of the cells had undergone division (even in the absence of serum). In contrast, fewer of the cells from the three low-malignant lines attached and spread on the plastic or collagen substrates in the absence of serum or in the presence of 0.1 per cent serum. However, when 15 μ g laminin per dish was added along with the lowmalignant cells, they then attached and spread on the plastic and collagen-coated dishes. Previous studies have indicated that the highly malignant lines express cell surface antigens that cross-react with laminin while the low-malignant cell lines do not. We speculate that the differences between the high- and low-malignant cells in the expression of cell surface laminin-like antigens contribute to the dissimilarities in attachment and spreading capacity. These differences may also contribute to the dissimilarity between these cells in malignant potential.en_US
dc.format.extent2084533 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers; Taylor & Francis Ltd ; Springer Science+Business Mediaen_US
dc.subject.otherMedicine & Public Healthen_US
dc.subject.otherCancer Researchen_US
dc.subject.otherHematologyen_US
dc.subject.otherOncologyen_US
dc.subject.otherSurgical Oncologyen_US
dc.titleAttachment, spreading and growth in vitro of highly malignant and low malignant murine fibrosarcoma cellsen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelOncology and Hematologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pathology, The University of Michigan Medical School, 48109, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Biological Chemistry, The University of Michigan Medical School, 48109, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Pathology, The University of Michigan Medical School, 48109, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationotherInstitute of Pathology, University of Oslo, Rikshospitalet-The National Hospital, N-0027, Oslo 1, Norwayen_US
dc.contributor.affiliationotherInstitute of Pathology, University of Oslo, Rikshospitalet-The National Hospital, N-0027, Oslo 1, Norwayen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid4042456en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/42592/1/10585_2005_Article_BF01758953.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF01758953en_US
dc.identifier.sourceClinical & Experimental Metastasisen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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