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Article: Nur77 as a survival factor in tumor necrosis factor signaling

TitleNur77 as a survival factor in tumor necrosis factor signaling
Authors
Issue Date2003
Citation
Proceedings of the National Academy of Sciences of the United States of America, 2003, v. 100, n. 14, p. 8276-8280 How to Cite?
AbstractThe immediate-early gene Nur77, which encodes an orphan nuclear receptor, is rapidly induced by various stress stimuli, including tumor necrosis factor (TNF). Nur77 has been implicated in mediating apoptosis, particularly in T cells and tumor cells. We report here that Nur77 can play a role in antagonizing apoptosis in TNF signaling. Nur77 expression is strongly induced by TNF. Interestingly, unlike most antiapoptotic molecules, this induced expression of Nur77 is largely independent of NF-κB. Ectopic expression of Nur77 can protect wild-type, TRAF2-/-, and RelA-/- cells from apoptosis induced by TNF, whereas expression of a dominant-negative form of Nur77 (DN-Nur77) accelerates TNF-mediated cell death in the mutant cells. In mouse embryonic fibroblasts, Nur77 remains in the nucleus in response to TNF and is not translocated to the mitochondria, where it was reported to mediate apoptosis. Our results suggest that Nur77 is a survival effector protein in the context of TNF-mediated signaling.
Persistent Identifierhttp://hdl.handle.net/10722/292525
ISSN
2023 Impact Factor: 9.4
2023 SCImago Journal Rankings: 3.737
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorSuzuki, Shinobu-
dc.contributor.authorSuzuki, Nobutaka-
dc.contributor.authorMirtsos, Christine-
dc.contributor.authorHoracek, Thomas-
dc.contributor.authorLye, Elizabeth-
dc.contributor.authorNoh, Seo Kyu-
dc.contributor.authorHo, Alexandra-
dc.contributor.authorBouchard, Denis-
dc.contributor.authorMak, Tak W.-
dc.contributor.authorYeh, Wen Chen-
dc.date.accessioned2020-11-17T14:56:40Z-
dc.date.available2020-11-17T14:56:40Z-
dc.date.issued2003-
dc.identifier.citationProceedings of the National Academy of Sciences of the United States of America, 2003, v. 100, n. 14, p. 8276-8280-
dc.identifier.issn0027-8424-
dc.identifier.urihttp://hdl.handle.net/10722/292525-
dc.description.abstractThe immediate-early gene Nur77, which encodes an orphan nuclear receptor, is rapidly induced by various stress stimuli, including tumor necrosis factor (TNF). Nur77 has been implicated in mediating apoptosis, particularly in T cells and tumor cells. We report here that Nur77 can play a role in antagonizing apoptosis in TNF signaling. Nur77 expression is strongly induced by TNF. Interestingly, unlike most antiapoptotic molecules, this induced expression of Nur77 is largely independent of NF-κB. Ectopic expression of Nur77 can protect wild-type, TRAF2-/-, and RelA-/- cells from apoptosis induced by TNF, whereas expression of a dominant-negative form of Nur77 (DN-Nur77) accelerates TNF-mediated cell death in the mutant cells. In mouse embryonic fibroblasts, Nur77 remains in the nucleus in response to TNF and is not translocated to the mitochondria, where it was reported to mediate apoptosis. Our results suggest that Nur77 is a survival effector protein in the context of TNF-mediated signaling.-
dc.languageeng-
dc.relation.ispartofProceedings of the National Academy of Sciences of the United States of America-
dc.titleNur77 as a survival factor in tumor necrosis factor signaling-
dc.typeArticle-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1073/pnas.0932598100-
dc.identifier.pmid12815108-
dc.identifier.pmcidPMC166219-
dc.identifier.scopuseid_2-s2.0-0038492453-
dc.identifier.volume100-
dc.identifier.issue14-
dc.identifier.spage8276-
dc.identifier.epage8280-
dc.identifier.isiWOS:000184222500044-
dc.identifier.issnl0027-8424-

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