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dc.contributor.authorAskautrud, Hanne Arenberg
dc.contributor.authorGjernes, Elisabet
dc.contributor.authorGunnes, Gjermund
dc.contributor.authorSletten, Marit
dc.contributor.authorRoss, D. T.
dc.contributor.authorBørresen-Dale, Anne-Lise
dc.contributor.authorIversen, Nina
dc.contributor.authorTranulis, Michael A.
dc.contributor.authorFrengen, Eirik
dc.date.accessioned2015-04-01T10:21:40Z
dc.date.accessioned2015-05-08T07:40:51Z
dc.date.available2015-04-01T10:21:40Z
dc.date.available2015-05-08T07:40:51Z
dc.date.issued2014
dc.identifier.citationPLoS ONE 2014, 9(1)nb_NO
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/11250/283317
dc.description-nb_NO
dc.description.abstractN-myc downstream-regulated gene 1 (NDRG1) is induced by cellular stress such as hypoxia and DNA damage, and in humans, germ line mutations cause Charcot-Marie-Tooth disease. However, the cellular roles of NDRG1 are not fully understood. Previously, NDRG1 was shown to mediate doxorubicin resistance under hypoxia, suggesting a role for NDRG1 in cell survival under these conditions. We found decreased apoptosis in doxorubicin-treated cells expressing NDRG1 shRNAs under normoxia, demonstrating a requirement for NDRG1 in apoptosis in breast epithelial cells under normal oxygen pressure. Also, different cellular stress regimens, such as hypoxia and doxorubicin treatment, induced NDRG1 through different stress signalling pathways. We further compared expression profiles in human breast epithelial cells ectopically over-expressing NDRG1 with cells expressing NDRG1 shRNAs in order to identify biological pathways where NDRG1 is involved. The results suggest that NDRG1 may have roles connected to vesicle transport.nb_NO
dc.language.isoengnb_NO
dc.rightsNavngivelse 3.0 Norge*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/no/*
dc.titleGlobal gene expression analysis reveals a link between NDRG1 and vesicle transportnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.date.updated2015-04-01T10:21:40Z
dc.identifier.doi10.1371/journal.pone.0087268
dc.identifier.cristin1148766


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