NLRX1 suppresses tumorigenesis and attenuates histiocytic sarcoma through the negative regulation of NF-lambda B signaling

dc.contributor.authorCoutermarsh-Ott, Sherylen
dc.contributor.authorSimmons, Alyshaen
dc.contributor.authorCapria, Vittoriaen
dc.contributor.authorLeRoith, Tanyaen
dc.contributor.authorWilson, Justin E.en
dc.contributor.authorHeid, Bettinaen
dc.contributor.authorPhilipson, Casandra W.en
dc.contributor.authorQin, Q.en
dc.contributor.authorHontecillas, Raquelen
dc.contributor.authorBassaganya-Riera, Josepen
dc.contributor.authorTing, Jenny P.-Y.en
dc.contributor.authorDervisis, Nikolaos G.en
dc.contributor.authorAllen, Irving C.en
dc.contributor.departmentBiological Sciencesen
dc.contributor.departmentSmall Animal Clinical Sciencesen
dc.date.accessioned2016-11-15T20:47:06Zen
dc.date.available2016-11-15T20:47:06Zen
dc.date.issued2016-05-31en
dc.description.abstractHistiocytic sarcoma is an uncommon malignancy in both humans and veterinary species. Research exploring the pathogenesis of this disease is scarce; thus, diagnostic and therapeutic options for patients are limited. Recent publications have suggested a role for the NLR, NLRX1, in acting as a tumor suppressor. Based on these prior findings, we hypothesized that NLRX1 would function to inhibit tumorigenesis and thus the development of histiocytic sarcoma. To test this, we utilized Nlrx1<sup>-/-</sup> mice and a model of urethane-induced tumorigenesis. Nlrx1<sup>-/-</sup> mice exposed to urethane developed splenic histiocytic sarcoma that was associated with significant up-regulation of the NF-kB signaling pathway. Additionally, development of these tumors was also significantly associated with the increased regulation of genes associated with AKT signaling, cell death and autophagy. Together, these data show that NLRX1 suppresses tumorigenesis and reveals new genetic pathways involved in the pathobiology of histiocytic sarcoma.en
dc.description.versionPublished versionen
dc.format.extent33096 - 33110 (15) page(s)en
dc.format.mimetypeapplication/pdfen
dc.identifier.doihttps://doi.org/10.18632/oncotarget.8861en
dc.identifier.issn1949-2553en
dc.identifier.issue22en
dc.identifier.urihttp://hdl.handle.net/10919/73447en
dc.identifier.volume7en
dc.language.isoenen
dc.publisherImpact Journalsen
dc.relation.urihttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000377748500116&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=930d57c9ac61a043676db62af60056c1en
dc.rightsCreative Commons Attribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.subjectOncologyen
dc.subjectCell Biologyen
dc.subjectNLRen
dc.subjectNod-like receptoren
dc.subjecturethaneen
dc.subjectcanceren
dc.subjectinflammationen
dc.subjectINFLAMMATORY-BOWEL-DISEASEen
dc.subjectNONSMALL CELL LUNGen
dc.subjectTUMOR-SUPPRESSORen
dc.subjectCOLON TUMORIGENESISen
dc.subjectI INTERFERONen
dc.subjectCANCER-CELLSen
dc.subjectPATHWAYen
dc.subjectPROTEINen
dc.subjectGROWTHen
dc.subjectCARCINOGENESISen
dc.titleNLRX1 suppresses tumorigenesis and attenuates histiocytic sarcoma through the negative regulation of NF-lambda B signalingen
dc.title.serialOncoTargeten
dc.typeArticle - Refereeden
dc.type.dcmitypeTexten
pubs.organisational-group/Virginia Techen
pubs.organisational-group/Virginia Tech/All T&R Facultyen
pubs.organisational-group/Virginia Tech/Faculty of Health Sciencesen
pubs.organisational-group/Virginia Tech/University Research Institutesen
pubs.organisational-group/Virginia Tech/University Research Institutes/Biocomplexity Instituteen
pubs.organisational-group/Virginia Tech/University Research Institutes/Biocomplexity Institute/Researchersen
pubs.organisational-group/Virginia Tech/University Research Institutes/Biocomplexity Institute/SelectedFaculty1en
pubs.organisational-group/Virginia Tech/Veterinary Medicineen
pubs.organisational-group/Virginia Tech/Veterinary Medicine/CVM T&R Facultyen
pubs.organisational-group/Virginia Tech/Veterinary Medicine/Small Animal Clinical Sciencesen

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