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dc.contributor.authorReinhardt, H. Christian
dc.contributor.authorJiang, Hai
dc.contributor.authorHemann, Michael
dc.contributor.authorYaffe, Michael B
dc.date.accessioned2012-10-04T19:49:54Z
dc.date.available2012-10-04T19:49:54Z
dc.date.issued2009-10
dc.date.submitted2009-07
dc.identifier.issn1538-4101
dc.identifier.urihttp://hdl.handle.net/1721.1/73619
dc.descriptionMarch 15, 2011en_US
dc.description.abstractEmerging data suggests that synthetic lethal interactions between mutated oncogenes/tumor suppressor genes and molecules involved in DNA damage signaling and repair can be therapeutically exploited to preferentially kill tumor cells. In this review, we discuss the concept of synthetic lethality, and describe several recent examples in which this concept was successfully implemented to target tumor cells in culture, in mouse models, and in human cancer patients.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant GM68762)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant CA112967)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant ES015339)en_US
dc.description.sponsorshipNational Cancer Institute (U.S.). Integrative Cancer Biology Program (Grant U54-CA112967-03)en_US
dc.description.sponsorshipGerman Research Foundation (RE2246/1-1)en_US
dc.description.sponsorshipDavid H. Koch Cancer Research Funden_US
dc.description.sponsorshipGerman Kidney Foundationen_US
dc.language.isoen_US
dc.publisherLandes Bioscienceen_US
dc.relation.isversionofhttp://dx.doi.org/10.4161/cc.8.19.9626en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourcePMCen_US
dc.titleExploiting synthetic lethal interactions for targeted cancer therapyen_US
dc.typeArticleen_US
dc.identifier.citationReinhardt, H. Christian et al. “Exploiting Synthetic Lethal Interactions for Targeted Cancer Therapy.” Cell Cycle 8.19 (2009): 3112–3119.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorJiang, Hai
dc.contributor.mitauthorHemann, Michael
dc.contributor.mitauthorYaffe, Michael B.
dc.contributor.mitauthorReinhardt, H. Christian
dc.relation.journalCell Cycleen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsReinhardt, H. Christian; Jiang, Hai; Hemann, Michael; Yaffe, Michael B.en
dc.identifier.orcidhttps://orcid.org/0000-0002-9547-3251
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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