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dc.contributor.authorTang, Yun-Chi
dc.contributor.authorWilliams, Bret R.
dc.contributor.authorSiegel, Jake J.
dc.contributor.authorAmon, Angelika B
dc.date.accessioned2013-12-10T21:56:24Z
dc.date.available2013-12-10T21:56:24Z
dc.date.issued2011-02
dc.date.submitted2010-11
dc.identifier.issn00928674
dc.identifier.urihttp://hdl.handle.net/1721.1/82911
dc.description.abstractAneuploidy, an incorrect chromosome number, is a hallmark of cancer. Compounds that cause lethality in aneuploid, but not euploid, cells could therefore provide new cancer therapies. We have identified the energy stress-inducing agent AICAR, the protein folding inhibitor 17-AAG, and the autophagy inhibitor chloroquine as exhibiting this property. AICAR induces p53-mediated apoptosis in primary mouse embryonic fibroblasts (MEFs) trisomic for chromosome 1, 13, 16, or 19. AICAR and 17-AAG, especially when combined, also show efficacy against aneuploid human cancer cell lines. Our results suggest that compounds that interfere with pathways that are essential for the survival of aneuploid cells could serve as a new treatment strategy against a broad spectrum of human tumors.en_US
dc.description.sponsorshipHoward Hughes Medical Instituteen_US
dc.description.sponsorshipMassachusetts Institute of Technology. School of Science (Curt W. and Kathy Marble Cancer Research Fund)en_US
dc.language.isoen_US
dc.publisherElsevier B.V.en_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.cell.2011.01.017en_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.sourceElsevier Open Archiveen_US
dc.titleIdentification of Aneuploidy-Selective Antiproliferation Compoundsen_US
dc.typeArticleen_US
dc.identifier.citationTang, Yun-Chi, Bret R. Williams, Jake J. Siegel, and Angelika Amon. “Identification of Aneuploidy-Selective Antiproliferation Compounds.” Cell 144, no. 4 (February 2011): 499-512.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorTang, Yun-Chien_US
dc.contributor.mitauthorWilliams, Bret R.en_US
dc.contributor.mitauthorSiegel, Jake J.en_US
dc.contributor.mitauthorAmon, Angelika B.en_US
dc.relation.journalCellen_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.orderedauthorsTang, Yun-Chi; Williams, Bret R.; Siegel, Jake J.; Amon, Angelikaen_US
dc.identifier.orcidhttps://orcid.org/0000-0001-9837-0314
dc.identifier.orcidhttps://orcid.org/0000-0003-0755-1369
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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