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Common origins of MDA-MB-435 cells from various sources with those shown to have melonoma properties

dc.contributor.authorRae, James Michaelen_US
dc.contributor.authorRamus, Susan J.en_US
dc.contributor.authorWaltham, Marken_US
dc.contributor.authorArmes, Jane E.en_US
dc.contributor.authorCampbell, Ian G.en_US
dc.contributor.authorClarke, Roberten_US
dc.contributor.authorBarndt, Robert J.en_US
dc.contributor.authorJohnson, Michael D.en_US
dc.contributor.authorThompson, Erik W.en_US
dc.date.accessioned2006-09-08T20:30:25Z
dc.date.available2006-09-08T20:30:25Z
dc.date.issued2004-12en_US
dc.identifier.citationRae, James M.; Ramus, Susan J.; Waltham, Mark; Armes, Jane E.; Campbell, Ian G.; Clarke, Robert; Barndt, Robert J.; Johnson, Michael D.; Thompson, Erik W.; (2004). "Common origins of MDA-MB-435 cells from various sources with those shown to have melonoma properties." Clinical & Experimental Metastasis 21(6): 543-552. <http://hdl.handle.net/2027.42/42591>en_US
dc.identifier.issn0262-0898en_US
dc.identifier.issn1573-7276en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/42591
dc.description.abstractRecently, the tissue origin of MDA-MB-435 cell line has been the subject of considerable debate. In this study, we set out to determine whether MDA-MB-435-DTP cells shown to express melanoma-specific genes were identical to various other MDA-MB-435 cell stocks worldwide. CGH-microarray, genetic polymorphism genotyping, microsatellite fingerprint analysis and/or chromosomal number confirmed that the MDA-MB-435 cells maintained at the Lombardi Comprehensive Cancer Center (MDA-MB-435-LCC) are almost identical to the MDA-MB-435-DTP cells, and showed a very similar profile to those obtained from the same original source (MD Anderson Cancer Center) but maintained independently (MDA-MB-435-PMCC). Gene expression profile analysis confirmed common expression of genes among different MDA-MB-435-LCC cell stocks, and identified some unique gene products in MDA-MB-435-PMCC cells. RT-PCR analysis confirmed the expression of the melanoma marker tyrosinase across multiple MDA-MB-435 cell stocks. Collectively, our results show that the MDA-MB-435 cells used widely have identical origins to those that exhibit a melanoma-like gene expression signature, but exhibit a small degree of genotypic and phenotypic drift.en_US
dc.format.extent289677 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers; Springer Science+Business Mediaen_US
dc.subject.otherMedicine & Public Healthen_US
dc.subject.otherCancer Researchen_US
dc.subject.otherOncologyen_US
dc.subject.otherHematologyen_US
dc.subject.otherSurgical Oncologyen_US
dc.subject.otherMDA-MB-435en_US
dc.subject.otherBreast Canceren_US
dc.subject.otherCell Linesen_US
dc.subject.otherMelanomaen_US
dc.subject.otherMicrosatellite Analysisen_US
dc.subject.otherChromosomal Numberen_US
dc.subject.otherTyrosinaseen_US
dc.titleCommon origins of MDA-MB-435 cells from various sources with those shown to have melonoma propertiesen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelOncology and Hematologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Internal Medicine, , University of Michigan, , , Ann Arbor, , Michigan, , USA,en_US
dc.contributor.affiliationumDepartment of Internal Medicine, , University of Michigan, , , Ann Arbor, , Michigan, , USA,en_US
dc.contributor.affiliationumDepartment of Internal Medicine, , University of Michigan, , , Ann Arbor, , Michigan, , USA,en_US
dc.contributor.affiliationumDepartment of Internal Medicine, , University of Michigan, , , Ann Arbor, , Michigan, , USA,en_US
dc.contributor.affiliationumDepartment of Internal Medicine, , University of Michigan, , , Ann Arbor, , Michigan, , USA,en_US
dc.contributor.affiliationumDepartment of Internal Medicine, , University of Michigan, , , Ann Arbor, , Michigan, , USA,en_US
dc.contributor.affiliationumDepartment of Internal Medicine, , University of Michigan, , , Ann Arbor, , Michigan, , USA,en_US
dc.contributor.affiliationumDepartment of Internal Medicine, , University of Michigan, , , Ann Arbor, , Michigan, , USA,en_US
dc.contributor.affiliationumDepartment of Internal Medicine, , University of Michigan, , , Ann Arbor, , Michigan, , USA,en_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid15679052en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/42591/1/10585_2004_Article_DO00003759.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/s10585-004-3759-1en_US
dc.identifier.sourceClinical & Experimental Metastasisen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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