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dc.rights.licenseopenen_US
dc.contributor.authorPERRIN-COCON, Laure
dc.contributor.authorVIDALAIN, Pierre-Olivier
dc.contributor.authorJACQUEMIN, Clemence
dc.contributor.authorAUBLIN-GEX, Anne
dc.contributor.authorOLMSTEAD, Keedrian
dc.contributor.authorPANTHU, Baptiste
dc.contributor.authorRAUTUREAU, Gilles Jeans Philippe
dc.contributor.authorANDRE, Patrice
dc.contributor.authorNYCZKA, Piotr
dc.contributor.authorHUTT, Marc-Thorsten
hal.structure.identifierCentre Génomique Fonctionnelle Bordeaux [Bordeaux] [CGFB]
dc.contributor.authorAMOEDO, Nivea Dias
hal.structure.identifierLaboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux) [U1211 INSERM/MRGM]
dc.contributor.authorROSSIGNOL, Rodrigue
dc.contributor.authorFILIPP, Fabian Volker
dc.contributor.authorLOTTEAU, Vincent
dc.contributor.authorDIAZ, Olivier
dc.date.accessioned2021-10-26T08:55:31Z
dc.date.available2021-10-26T08:55:31Z
dc.date.issued2021-02-16
dc.identifier.issn2399-3642en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/112872
dc.description.abstractEnDuring the cancerous transformation of normal hepatocytes into hepatocellular carcinoma (HCC), the enzyme catalyzing the first rate-limiting step of glycolysis, namely the glucokinase (GCK), is replaced by the higher affinity isoenzyme, hexokinase 2 (HK2). Here, we show that in HCC tumors the highest expression level of HK2 is inversely correlated to GCK expression, and is associated to poor prognosis for patient survival. To further explore functional consequences of the GCK-to-HK2 isoenzyme switch occurring during carcinogenesis, HK2 was knocked-out in the HCC cell line Huh7 and replaced by GCK, to generate the Huh7-GCK+/HK2? cell line. HK2 knockdown and GCK expression rewired central carbon metabolism, stimulated mitochondrial respiration and restored essential metabolic functions of normal hepatocytes such as lipogenesis, VLDL secretion, glycogen storage. It also reactivated innate immune responses and sensitivity to natural killer cells, showing that consequences of the HK switch extend beyond metabolic reprogramming.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.title.enA hexokinase isoenzyme switch in human liver cancer cells promotes lipogenesis and enhances innate immunity
dc.typeArticle de revueen_US
dc.identifier.doi10.1038/s42003-021-01749-3en_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologieen_US
dc.identifier.pubmed33594203en_US
bordeaux.journalCommunications Biologyen_US
bordeaux.volume4en_US
bordeaux.hal.laboratoriesMaladies Rares : Génétique et Métabolisme (MRGM) - UMR 1211en_US
bordeaux.issue1en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.identifier.funderIDFondation pour la Recherche Médicaleen_US
hal.identifierhal-03403454
hal.version1
hal.date.transferred2021-10-26T08:55:37Z
hal.exporttrue
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Communications%20Biology&rft.date=2021-02-16&rft.volume=4&rft.issue=1&rft.eissn=2399-3642&rft.issn=2399-3642&rft.au=PERRIN-COCON,%20Laure&VIDALAIN,%20Pierre-Olivier&JACQUEMIN,%20Clemence&AUBLIN-GEX,%20Anne&OLMSTEAD,%20Keedrian&rft.genre=article


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