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dc.contributor.authorVander Heiden, Matthew G.
dc.date.accessioned2013-01-08T14:38:57Z
dc.date.available2013-01-08T14:38:57Z
dc.date.issued2011-09
dc.identifier.issn1474-1784
dc.identifier.urihttp://hdl.handle.net/1721.1/76182
dc.description.abstractGenetic events in cancer activate signalling pathways that alter cell metabolism. Clinical evidence has linked cell metabolism with cancer outcomes. Together, these observations have raised interest in targeting metabolic enzymes for cancer therapy, but they have also raised concerns that these therapies would have unacceptable effects on normal cells. However, some of the first cancer therapies that were developed target the specific metabolic needs of cancer cells and remain effective agents in the clinic today. Research into how changes in cell metabolism promote tumour growth has accelerated in recent years. This has refocused efforts to target metabolic dependencies of cancer cells as a selective anticancer strategy.en_US
dc.description.sponsorshipBurroughs Wellcome Funden_US
dc.description.sponsorshipSmith Family Foundationen_US
dc.description.sponsorshipStarr Cancer Consortiumen_US
dc.description.sponsorshipDamon Runyon Cancer Research Foundationen_US
dc.description.sponsorshipNational Institutes of Health (U.S.)en_US
dc.language.isoen_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/nrd3504en_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.sourceVander Heiden via Courtney Crummetten_US
dc.titleTargeting cancer metabolism: a therapeutic window opensen_US
dc.typeArticleen_US
dc.identifier.citationVander Heiden, Matthew G. “Targeting Cancer Metabolism: a Therapeutic Window Opens.” Nature Reviews Drug Discovery 10.9 (2011): 671–684.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.approverVander Heiden, Matthew
dc.contributor.mitauthorVander Heiden, Matthew G.
dc.relation.journalNature Reviews Drug Discoveryen_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.orderedauthorsVander Heiden, Matthew G.en
dc.identifier.orcidhttps://orcid.org/0000-0002-6702-4192
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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