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dc.contributor.authorOlivares, Orianne
dc.contributor.authorMayers, Jared R.
dc.contributor.authorGouirand, Victoire
dc.contributor.authorTorrence, Margaret E.
dc.contributor.authorGicquel, Tristan
dc.contributor.authorBorge, Laurence
dc.contributor.authorLac, Sophie
dc.contributor.authorRoques, Julie
dc.contributor.authorLavaut, Marie-Noëlle
dc.contributor.authorBerthezène, Patrice
dc.contributor.authorRubis, Marion
dc.contributor.authorSecq, Veronique
dc.contributor.authorGarcia, Stéphane
dc.contributor.authorMoutardier, Vincent
dc.contributor.authorLombardo, Dominique
dc.contributor.authorIovanna, Juan Lucio
dc.contributor.authorTomasini, Richard
dc.contributor.authorGuillaumond, Fabienne
dc.contributor.authorVander Heiden, Matthew G.
dc.contributor.authorVasseur, Sophie
dc.date.accessioned2018-02-12T15:46:57Z
dc.date.available2018-02-12T15:46:57Z
dc.date.issued2017-07
dc.date.submitted2016-01
dc.identifier.issn2041-1723
dc.identifier.urihttp://hdl.handle.net/1721.1/113569
dc.description.abstractTissue architecture contributes to pancreatic ductal adenocarcinoma (PDAC) phenotypes. Cancer cells within PDAC form gland-like structures embedded in a collagen-rich meshwork where nutrients and oxygen are scarce. Altered metabolism is needed for tumour cells to survive in this environment, but the metabolic modifications that allow PDAC cells to endure these conditions are incompletely understood. Here we demonstrate that collagen serves as a proline reservoir for PDAC cells to use as a nutrient source when other fuels are limited. We show PDAC cells are able to take up collagen fragments, which can promote PDAC cell survival under nutrient limited conditions, and that collagen-derived proline contributes to PDAC cell metabolism. Finally, we show that proline oxidase (PRODH1) is required for PDAC cell proliferation in vitro and in vivo. Collectively, our results indicate that PDAC extracellular matrix represents a nutrient reservoir for tumour cells highlighting the metabolic flexibility of this cancer.en_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/NCOMMS16031en_US
dc.rightsCreative Commons Attribution 4.0 International Licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceNature Communicationsen_US
dc.titleCollagen-derived proline promotes pancreatic ductal adenocarcinoma cell survival under nutrient limited conditionsen_US
dc.typeArticleen_US
dc.identifier.citationOlivares, Orianne et al. “Collagen-Derived Proline Promotes Pancreatic Ductal Adenocarcinoma Cell Survival Under Nutrient Limited Conditions.” Nature Communications 8 (July 2017): 16031 © 2017 Author(s)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.mitauthorMayers, Jared R.
dc.contributor.mitauthorTorrence, Margaret E.
dc.contributor.mitauthorVander Heiden, Matthew G.
dc.relation.journalNature Communicationsen_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.updated2018-02-02T19:30:55Z
dspace.orderedauthorsOlivares, Orianne; Mayers, Jared R.; Gouirand, Victoire; Torrence, Margaret E.; Gicquel, Tristan; Borge, Laurence; Lac, Sophie; Roques, Julie; Lavaut, Marie-Noëlle; Berthezène, Patrice; Rubis, Marion; Secq, Veronique; Garcia, Stéphane; Moutardier, Vincent; Lombardo, Dominique; Iovanna, Juan Lucio; Tomasini, Richard; Guillaumond, Fabienne; Vander Heiden, Matthew G.; Vasseur, Sophieen_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-8607-1787
dc.identifier.orcidhttps://orcid.org/0000-0002-6702-4192
mit.licensePUBLISHER_POLICYen_US


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