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dc.date.accessioned2021-10-04T19:10:21Z
dc.date.available2021-10-04T19:10:21Z
dc.date.issued2021-04-01
dc.date.submitted2021-02-08
dc.identifier.issn2662-1347
dc.identifier.urihttps://hdl.handle.net/1721.1/132709
dc.description.abstractBrain metastases are refractory to therapies that control systemic disease in patients with human epidermal growth factor receptor 2 (HER2+) breast cancer, and the brain microenvironment contributes to this therapy resistance. Nutrient availability can vary across tissues, therefore metabolic adaptations required for brain metastatic breast cancer growth may introduce liabilities that can be exploited for therapy. Here, we assessed how metabolism differs between breast tumors in brain versus extracranial sites and found that fatty acid synthesis is elevated in breast tumors growing in brain. We determine that this phenotype is an adaptation to decreased lipid availability in brain relative to other tissues, resulting in a site-specific dependency on fatty acid synthesis for breast tumors growing at this site. Genetic or pharmacological inhibition of fatty acid synthase (FASN) reduces HER2+ breast tumor growth in the brain, demonstrating that differences in nutrient availability across metastatic sites can result in targetable metabolic dependencies.en_US
dc.language.isoen
dc.publisherSpringer Science and Business Media LLCen_US
dc.relation.isversionof10.1038/S43018-021-00183-Yen_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.sourcePMCen_US
dc.titleFatty acid synthesis is required for breast cancer brain metastasisen_US
dc.typeArticleen_US
dc.identifier.citationFerraro, G.B., Ali, A., Luengo, A. et al. Fatty acid synthesis is required for breast cancer brain metastasis. Nat Cancer 2, 414–428 (2021)en_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MIT
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biology
dc.relation.journalNature Canceren_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
dc.date.updated2021-10-04T17:18:45Z
dspace.orderedauthorsFerraro, GB; Ali, A; Luengo, A; Kodack, DP; Deik, A; Abbott, KL; Bezwada, D; Blanc, L; Prideaux, B; Jin, X; Possada, JM; Chen, J; Chin, CR; Amoozgar, Z; Ferreira, R; Chen, IX; Naxerova, K; Ng, C; Westermark, AM; Duquette, M; Roberge, S; Lindeman, NI; Lyssiotis, CA; Nielsen, J; Housman, DE; Duda, DG; Brachtel, E; Golub, TR; Cantley, LC; Asara, JM; Davidson, SM; Fukumura, D; Dartois, VA; Clish, CB; Jain, RK; Vander Heiden, MGen_US
dspace.date.submission2021-10-04T17:18:47Z
mit.journal.volume2en_US
mit.journal.issue4en_US
mit.licensePUBLISHER_POLICY
mit.metadata.statusAuthority Work Neededen_US


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