Publication:
Role of the chromobox protein CBX7 in lymphomagenesis.

dc.contributor.authorScott, Clare L
dc.contributor.authorGil, Jesús
dc.contributor.authorHernando, Eva
dc.contributor.authorTeruya-Feldstein, Julie
dc.contributor.authorNarita, Masako
dc.contributor.authorMartinez Garcia, Maria Dolores
dc.contributor.authorVisakorpi, Tapio
dc.contributor.authorMu, David
dc.contributor.authorCordon-Cardo, Carlos
dc.contributor.authorPeters, Gordon
dc.contributor.authorBeach, David
dc.contributor.authorLowe, Scott W
dc.contributor.funderWellcome Trust
dc.contributor.funderNational Cancer Center (Estados Unidos)
dc.date.accessioned2024-02-01T11:28:24Z
dc.date.available2024-02-01T11:28:24Z
dc.date.issued2007-03-27
dc.description.abstractChromobox 7 (CBX7) is a chromobox family protein and a component of the Polycomb repressive complex 1 (PRC1) that extends the lifespan of cultured epithelial cells and can act independently of BMI-1 to repress the INK4a/ARF tumor suppressor locus. To determine whether CBX7 might be oncogenic, we examined its expression pattern in a range of normal human tissues and tumor samples. CBX7 was expressed at high levels in germinal center lymphocytes and germinal center-derived follicular lymphomas, where elevated expression correlated with high c-Myc expression and a more advanced tumor grade. By targeting Cbx7 expression to the lymphoid compartment in mice, we showed that Cbx7 can initiate T cell lymphomagenesis and cooperate with c-Myc to produce highly aggressive B cell lymphomas. Furthermore, Cbx7 repressed transcription from the Ink4a/Arf locus and acted epistatically to the Arf-p53 pathway during tumorigenesis. These data identify CBX7 as a chromobox protein causally linked to cancer development and may help explain the low frequency of INK4a/ARF mutations observed in human follicular lymphoma.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipWe thank M. Roussel (St. Jude Children’s Research Hospital, Memphis,TN) for the p19Arf antibody and J. C. Acosta, M. Asher, I. Linkov, T. Matos, M. E. Dudas, D. Pant, E. Jansen, K. Campbell, R. Sachidanandam, M. Serrano, S. Powers, M. McCurrach, and M. Collado for assistance and helpful advice. C.L.S. was a Seligson Clinical Fellow and a Special Fellow of the Leukemia and Lymphoma Society of America and is currently supported by the Australian National Health and Medical Research Council (CDA 406675). D.M. was supported in part by a grant from Joan’s Legacy Foundation. This work is supported by the Don Monti Foundation, the Wellcome Trust (D.B.), the Medical Research Council (D.B. and J.G.), Cancer Research UK (G.P. and J.G.), the National Cancer Institute (C.C.-C. and S.W.L.), and the Leukemia and Lymphoma Society of America (S.W.L.).es_ES
dc.format.number13es_ES
dc.format.page5389es_ES
dc.format.volume104es_ES
dc.identifier.citationProc Natl Acad Sci U S A . 2007;104(13):5389-94.es_ES
dc.identifier.doi10.1073/pnas.0608721104es_ES
dc.identifier.issn0027-8424es_ES
dc.identifier.journalProceedings of the National Academy of Sciences of the United States of Americaes_ES
dc.identifier.pubmedID17374722es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/17407
dc.language.isoenges_ES
dc.publisherOxford University Press
dc.relation.publisherversionhttps://doi.org/10.1073/pnas.0608721104.es_ES
dc.repisalud.institucionCNIOes_ES
dc.repisalud.orgCNIOCNIO::Unidades técnicas::Unidad de Citometría de Flujoes_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.meshMutationes_ES
dc.subject.meshAnimalses_ES
dc.subject.meshCyclin-Dependent Kinase Inhibitor p16es_ES
dc.subject.meshEpithelial Cellses_ES
dc.subject.meshHumanses_ES
dc.subject.meshLoss of Heterozygosityes_ES
dc.subject.meshLymphomaes_ES
dc.subject.meshMicees_ES
dc.subject.meshNeoplasmses_ES
dc.subject.meshNuclear Proteinses_ES
dc.subject.meshPolycomb Repressive Complex 1es_ES
dc.subject.meshPolycomb-Group Proteinses_ES
dc.subject.meshProto-Oncogene Proteins c-myces_ES
dc.subject.meshRepressor Proteinses_ES
dc.subject.meshT-Lymphocyteses_ES
dc.subject.meshTumor Suppressor Protein p53es_ES
dc.titleRole of the chromobox protein CBX7 in lymphomagenesis.es_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
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