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dc.contributor.authorLuengo, Alba
dc.contributor.authorSullivan, Lucas Bryan
dc.contributor.authorVander Heiden, Matthew G.
dc.date.accessioned2014-11-14T18:55:06Z
dc.date.available2014-11-14T18:55:06Z
dc.date.issued2014-10
dc.identifier.issn1741-7007
dc.identifier.urihttp://hdl.handle.net/1721.1/91581
dc.description.abstractMetformin has been a first-line treatment for type II diabetes mellitus for decades and is the most widely prescribed antidiabetic drug. Retrospective studies have found that metformin treatment is associated with both reduced cancer diagnoses and cancer-related deaths. Despite the prevalence of metformin use in the clinic, its molecular mechanism of action remains controversial. In a recent issue of Cancer & Metabolism, Andrzejewski et al. present evidence that metformin acts directly on mitochondria to inhibit complex I and limits the ability of cancer cells to cope with energetic stress. Here, we discuss evidence that supports the role of metformin as a cancer therapeutic.en_US
dc.publisherBioMed Central Ltden_US
dc.relation.isversionofhttp://dx.doi.org/10.1186/s12915-014-0082-4en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0en_US
dc.sourceBioMed Central Ltden_US
dc.titleUnderstanding the complex-I-ty of metformin action: limiting mitochondrial respiration to improve cancer therapyen_US
dc.typeArticleen_US
dc.identifier.citationLuengo, Alba, Lucas B Sullivan, and Matthew G Vander Heiden. “Understanding the Complex-I-Ty of Metformin Action: Limiting Mitochondrial Respiration to Improve Cancer Therapy.” BMC Biology 12, no. 1 (October 24, 2014).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.mitauthorLuengo, Albaen_US
dc.contributor.mitauthorSullivan, Lucas Bryanen_US
dc.contributor.mitauthorVander Heiden, Matthew G.en_US
dc.relation.journalBMC Biologyen_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.updated2014-10-24T03:03:31Z
dc.language.rfc3066en
dc.rights.holderAlba Luengo et al.; licensee BioMed Central Ltd.
dspace.orderedauthorsLuengo, Alba; Sullivan, Lucas B; Heiden, Matthew G Vanderen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-6702-4192
dc.identifier.orcidhttps://orcid.org/0000-0002-4236-0229
dc.identifier.orcidhttps://orcid.org/0000-0002-6745-8222
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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