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dc.contributor.authorSu, Ying
dc.contributor.authorPolyak, Kornelia
dc.contributor.authorArendt, Lisa M.
dc.contributor.authorKuperwasser, Charlotte
dc.contributor.authorBierie, Brian
dc.contributor.authorChaffer, Christine L.
dc.contributor.authorBrueckmann, Ines
dc.contributor.authorScheel, Christina
dc.contributor.authorKaestli, Alicia J.
dc.contributor.authorWiggins, Paul A.
dc.contributor.authorRodrigues, Leonardo O.
dc.contributor.authorBrooks, Mary
dc.contributor.authorReinhardt, Ferenc
dc.contributor.authorWeinberg, Robert A
dc.date.accessioned2011-12-02T20:04:25Z
dc.date.available2011-12-02T20:04:25Z
dc.date.issued2011-04
dc.date.submitted2010-12
dc.identifier.issn0027-8424
dc.identifier.issn1091-6490
dc.identifier.urihttp://hdl.handle.net/1721.1/67358
dc.description.abstractCurrent models of stem cell biology assume that normal and neoplastic stem cells reside at the apices of hierarchies and differentiate into nonstem progeny in a unidirectional manner. Here we identify a subpopulation of basal-like human mammary epithelial cells that departs from that assumption, spontaneously dedifferentiating into stem-like cells. Moreover, oncogenic transformation enhances the spontaneous conversion, so that nonstem cancer cells give rise to cancer stem cell (CSC)-like cells in vitro and in vivo. We further show that the differentiation state of normal cells-of-origin is a strong determinant of posttransformation behavior. These findings demonstrate that normal and CSC-like cells can arise de novo from more differentiated cell types and that hierarchical models of mammary stem cell biology should encompass bidirectional interconversions between stem and nonstem compartments. The observed plasticity may allow derivation of patient-specific adult stem cells without genetic manipulation and holds important implications for therapeutic strategies to eradicate cancer.en_US
dc.description.sponsorshipNational Health and Medical Research Council (Australia)en_US
dc.description.sponsorshipNational Institutes of Health (NIH) (Grant U54 CA12515)en_US
dc.description.sponsorshipMassachusetts Institute of Technology. Ludwig Center for Molecular Oncologyen_US
dc.description.sponsorshipBreast Cancer Research Foundationen_US
dc.description.sponsorshipAdvanced Medical Technology Associationen_US
dc.description.sponsorshipUnited States. Dept. of Defense. Breast Cancer Research Program Idea Awarden_US
dc.language.isoen_US
dc.publisherNew York Academy of Sciencesen_US
dc.relation.isversionofhttp://dx.doi.org/10.1073/pnas.1102454108en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourcePNASen_US
dc.titleNormal and neoplastic non-stem cells can spontaneously convert to a stem-like stateen_US
dc.typeArticleen_US
dc.identifier.citationChaffer, C. L. et al. “Normal and neoplastic nonstem cells can spontaneously convert to a stem-like state.” Proceedings of the National Academy of Sciences 108 (2011): 7950-7955. Web. 2 Dec. 2011. © 2009 New York Academy of Sciencesen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentWhitehead Institute for Biomedical Researchen_US
dc.contributor.departmentLudwig Center for Molecular Oncology (Massachusetts Institute of Technology)en_US
dc.contributor.approverWeinberg, Robert A.
dc.contributor.mitauthorChaffer, Christine L.
dc.contributor.mitauthorBrueckmann, Ines
dc.contributor.mitauthorScheel, Christina
dc.contributor.mitauthorKaestli, Alicia J.
dc.contributor.mitauthorWiggins, Paul A.
dc.contributor.mitauthorRodrigues, Leonardo O.
dc.contributor.mitauthorBrooks, Mary
dc.contributor.mitauthorReinhardt, Ferenc
dc.contributor.mitauthorWeinberg, Robert A.
dc.relation.journalProceedings of the National Academy of Sciences of the United States of Americaen_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.orderedauthorsChaffer, C. L.; Brueckmann, I.; Scheel, C.; Kaestli, A. J.; Wiggins, P. A.; Rodrigues, L. O.; Brooks, M.; Reinhardt, F.; Su, Y.; Polyak, K.; Arendt, L. M.; Kuperwasser, C.; Bierie, B.; Weinberg, R. A.en
dc.identifier.orcidhttps://orcid.org/0000-0002-0895-3557
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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