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dc.contributor.authorJacqueline Salottien_US
dc.contributor.authorKrisada Sakchaisrien_US
dc.contributor.authorWarren G. Tourtellotteen_US
dc.contributor.authorPeter F. Johnsonen_US
dc.contributor.otherNational Cancer Institute at Fredericken_US
dc.contributor.otherNorthwestern University Feinberg School of Medicineen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-11-23T09:49:10Z-
dc.date.available2018-11-23T09:49:10Z-
dc.date.issued2015-01-01en_US
dc.identifier.citationMolecular and Cellular Biology. Vol.35, No.5 (2015), 866-883en_US
dc.identifier.issn10985549en_US
dc.identifier.issn02707306en_US
dc.identifier.other2-s2.0-84961290076en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84961290076&origin=inwarden_US
dc.identifier.urihttp://repository.li.mahidol.ac.th/dspace/handle/123456789/35582-
dc.description.abstract© 2015, American Society for Microbiology. Oncogene-induced senescence (OIS) protects normal cells from transformation by Ras, whereas cells lacking p14/p19Arfor other tumor suppressors can be transformed. The transcription factor C/EBPβ is required for OIS in primary fibroblasts but is downregulated by H-RasV12in immortalized NIH 3T3 cells through a mechanism involving p19Arfloss. Here, we report that members of the serum-induced early growth response (Egr) protein family are also downregulated in 3T3Rascells and directly and redundantly control Cebpb gene transcription. Egr1, Egr2, and Egr3 recognize three sites in the Cebpb promoter and associate transiently with this region after serum stimulation, coincident with Cebpb induction. Codepletion of all three Egrs prevented Cebpb expression, and serum induction of Egrs was significantly blunted in 3T3Rascells. Egr2 and Egr3 levels were also reduced in RasV12-expressing p19Arfnull mouse embryonic fibroblasts (MEFs), and overall Egr DNA-binding activity was suppressed in Arfdeficient but not wild-type (WT) MEFs, leading to Cebpb downregulation. Analysis of human cancers revealed a strong correlation between EGR levels and CEBPB expression, regardless of whether CEBPB was increased or decreased in tumors. Moreover, overexpression of Egrs in tumor cell lines induced CEBPB and inhibited proliferation. Thus, our findings identify the Arf-Egr-C/ EBPβ axis as an important determinant of cellular responses (senescence or transformation) to oncogenic Ras signaling.en_US
dc.rightsMahidol Universityen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84961290076&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleAn Arf-Egr-C/EBPβ pathway linked to ras-induced senescence and canceren_US
dc.typeArticleen_US
dc.rights.holderSCOPUSen_US
dc.identifier.doi10.1128/MCB.01489-14en_US
Appears in Collections:Scopus 2011-2015

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