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dc.contributor.authorHosios, Aaron M
dc.contributor.authorVander Heiden, Matthew G.
dc.date.accessioned2014-12-17T20:54:56Z
dc.date.available2014-12-17T20:54:56Z
dc.date.issued2014
dc.date.submitted2014-11
dc.identifier.issn2049-3002
dc.identifier.urihttp://hdl.handle.net/1721.1/92358
dc.description.abstractMacromolecule biosynthesis is required to duplicate cell components and support proliferation. Studies examining the nutrients used by cancer cells have focused on the contribution of glucose and glutamine carbon for biosynthesis, but the importance of other metabolic fuels is becoming apparent. Labeling of two-carbon units in newly synthesized lipids has been used to infer the nutrients that contribute to the acetyl-CoA pools in cells. Glucose- and glutamine-derived carbon are known to contribute extensively to de novo lipid biosynthesis, and in this issue Kamphorst et al. find that extracellular acetate can also contribute substantially to this process [1].en_US
dc.publisherBioMed Central Ltden_US
dc.relation.isversionofhttp://dx.doi.org/10.1186/s40170-014-0027-yen_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0en_US
dc.sourceBioMed Central Ltden_US
dc.titleAcetate metabolism in cancer cellsen_US
dc.typeArticleen_US
dc.identifier.citationHosios, Aaron M. and Matthew G. Vander Heiden. "Acetate metabolism in cancer cells." Cancer & Metabolism 2014, 2:27.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.mitauthorVander Heiden, Matthew G.en_US
dc.relation.journalCancer & Metabolismen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2014-12-11T20:50:31Z
dc.language.rfc3066en
dc.rights.holderAaron M Hosios et al.; licensee BioMed Central Ltd.
dspace.orderedauthorsHosios, Aaron M.; Vander Heiden, Matthew G.en_US
dc.identifier.orcidhttps://orcid.org/0000-0002-6702-4192
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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