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dc.contributor.authorCristea, S
dc.contributor.authorColes, GL
dc.contributor.authorHornburg, D
dc.contributor.authorGershkovitz, M
dc.contributor.authorArand, J
dc.contributor.authorCao, S
dc.contributor.authorSen, T
dc.contributor.authorWilliamson, Stuart
dc.contributor.authorKim, JW
dc.contributor.authorDrainas, AP
dc.contributor.authorHe, A
dc.contributor.authorLe Cam, L
dc.contributor.authorByers, LA
dc.contributor.authorSnyder, MP
dc.contributor.authorContrepois, K
dc.contributor.authorSage, J
dc.date.accessioned2020-02-27T16:55:25Z
dc.date.available2020-02-27T16:55:25Z
dc.date.issued2020en
dc.identifier.citationCristea S, Coles GL, Hornburg D, Gershkovitz M, Arand J, Cao S, et al. The MEK5-ERK5 kinase axis controls lipid metabolism in small cell lung cancer. Cancer Res. 2020.en
dc.identifier.pmid31969375en
dc.identifier.doi10.1158/0008-5472.CAN-19-1027en
dc.identifier.urihttp://hdl.handle.net/10541/622762
dc.description.abstractSmall cell lung cancer (SCLC) is an aggressive form of lung cancer with dismal survival rates. While kinases often play key roles driving tumorigenesis, there are strikingly few kinases known to promote the development of SCLC. Here we investigated the contribution of the MAP kinase module MEK5/ERK5 to SCLC growth. MEK5 and ERK5 were required for optimal survival and expansion of SCLC cell lines in vitro and in vivo. Transcriptomics analyses identified a role for the MEK5-ERK5 axis in the metabolism of SCLC cells, including lipid metabolism. In-depth lipidomics analyses showed that loss of MEK5/ERK5 perturbs several lipid metabolism pathways, including the mevalonate pathway that controls cholesterol synthesis. Notably, depletion of MEK5/ERK5 sensitized SCLC cells to pharmacological inhibition of the mevalonate pathway by statins. These data identify a new MEK5-ERK5-lipid metabolism axis that promotes the growth of SCLC.en
dc.language.isoenen
dc.relation.urlhttps://dx.doi.org/10.1158/0008-5472.CAN-19-1027en
dc.titleThe MEK5-ERK5 kinase axis controls lipid metabolism in small cell lung canceren
dc.typeArticleen
dc.contributor.departmentPediatrics and Genetics, Stanford Universityen
dc.identifier.journalCancer Researchen
dc.description.noteen]
refterms.dateFOA2020-03-04T11:08:38Z


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