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dc.date.accessioned2015-04-13T18:13:11Z
dc.date.available2015-04-13T18:13:11Z
dc.date.created2014-08-22T12:46:38Z
dc.date.issued2014
dc.identifier.citationAskautrud, Hanne Arenberg Gjernes, Elisabet Gunnes, Gjermund Sletten, Marit Ross, D. T. Børresen-Dale, Anne-Lise Iversen, Nina Tranulis, Michael A. Frengen, Eirik . Global Gene Expression Analysis Reveals a Link between NDRG1 and Vesicle Transport. PLoS ONE. 2014, 9(1)
dc.identifier.urihttp://hdl.handle.net/10852/43550
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.en_US
dc.languageEN
dc.language.isoenen_US
dc.publisherPublic Library of Science (PLoS)
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleGlobal Gene Expression Analysis Reveals a Link between NDRG1 and Vesicle Transporten_US
dc.typeJournal articleen_US
dc.creator.authorAskautrud, Hanne Arenberg
dc.creator.authorGjernes, Elisabet
dc.creator.authorGunnes, Gjermund
dc.creator.authorSletten, Marit
dc.creator.authorRoss, D. T.
dc.creator.authorBørresen-Dale, Anne-Lise
dc.creator.authorIversen, Nina
dc.creator.authorTranulis, Michael A.
dc.creator.authorFrengen, Eirik
cristin.unitcode185,53,18,10
cristin.unitnameAvdeling for medisinsk genetikk
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.cristin1148766
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=PLoS ONE&rft.volume=9&rft.spage=&rft.date=2014
dc.identifier.jtitlePLoS ONE
dc.identifier.volume9
dc.identifier.issue1
dc.identifier.doihttp://dx.doi.org/10.1371/journal.pone.0087268
dc.identifier.urnURN:NBN:no-47921
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn1932-6203
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/43550/1/journal-pone-0087268frengen.pdf
dc.type.versionPublishedVersion
cristin.articleide87268


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