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dc.contributor.authorBordas, Anna
dc.contributor.authorCedillo, José Luis
dc.contributor.authorArnalich Fernández, Francisco 
dc.contributor.authorEsteban-Rodríguez, Isabel
dc.contributor.authorGuerra-Pastrián, Laura
dc.contributor.authorCastro, Javier de
dc.contributor.authorMartín-Sánchez, Carolina
dc.contributor.authorAtienza, Gema
dc.contributor.authorFernández Capitán, María del Carmen 
dc.contributor.authorRíos Blanco, Juan José 
dc.contributor.authorMontiel López, Carmen 
dc.contributor.otherUAM. Departamento de Farmacologíaes_ES
dc.contributor.otherUAM. Departamento de Medicinaes_ES
dc.contributor.otherInstituto de Investigación Sanitaria Hospital Universitario de La Paz (IdiPAZ)es_ES
dc.date.accessioned2017-11-14T17:50:23Z
dc.date.available2017-11-14T17:50:23Z
dc.date.issued2017-07-04
dc.identifier.citationOncotarget 8.40 (2017): 67878-67890en_US
dc.identifier.issn1949-2553es_ES
dc.identifier.urihttp://hdl.handle.net/10486/680233
dc.description.abstractCigarette smoking is associated with increased risk for all histologic types of lung cancer, but why the strength of this association is stronger for squamous cell carcinoma than adenocarcinoma of the lung (SQC-L, ADC-L) is not fully understood. Because nicotine and tobacco-specific nitrosamines contribute to carcinogenesis by activating nicotinic acetylcholine receptors (nAChRs) on lung tumors and epithelial cells, we investigated whether differential expression of nAChR subtypes in these tumors could explain their different association with smoking. Expression of nAChR subunit genes in paired tumor and non-tumor lung specimens from 40 SQC-L and 38 ADC-L patients was analyzed by quantitative PCR. Compared to normal lung, both tumors share: i) transcriptional dysregulation of CHRNA3/CHRNA5/CHRNB4 (α3, α5, β4 subunits) at the chromosomal locus that predisposes to lung cancer; and ii) decreased expression of CHRFAM7A (dupα7 subunit); this last subunit negatively modulates α7-nAChR activity in oocytes. In contrast, CHRNA7 (α7 subunit) expression was increased in SQC-L, particularly in smokers and non-survivors, while CHRNA4 (α4 subunit) expression was decreased in ADC-L. Thus, over-representation of cancer-stimulating α7-nAChR in SQC-L, also potentiated by smoking, and underrepresentation of cancer-inhibiting α4β2-nAChR in ADC-L could explain the different tobacco influences on the tumorigenic process in each cancer typeen_US
dc.description.sponsorshipThis study was supported by grants to C. Montiel and F. Arnalich from the Ministry of Economy, Industry and Competitiveness, Government of Spain (SAF2014-56623-R) and Foundation “Mutua Madrileña Investigación Biomédica” (FMM2011), Spain. A.B. is recipient of a fellowship (Beca FPI, Universidad Autónoma Madrid). J.L.C. and C.M.S. are recipients of fellowships (Beca FPU from Ministerio de Educación, Cultura y Deporte and Beca FPI from Ministry of Economy, Industry and Competitiveness, Government of Spain, respectively)en_US
dc.format.extent13 pag.es_ES
dc.format.mimetypeapplication/pdfen
dc.language.isoengen
dc.publisherImpact Journals LLCen_US
dc.relation.ispartofOncotargeten_US
dc.rights© Bordas et al.es_ES
dc.subject.othernAChRsen_US
dc.subject.otherNSCLCen_US
dc.subject.otherSquamous cell carcinoma of the lungen_US
dc.subject.otherLung adenocarcinomaen_US
dc.subject.otherTobaccoen_US
dc.titleExpression patterns for nicotinic acetylcholine receptor subunit genes in smoking-related lung cancersen_US
dc.typearticleen
dc.subject.ecienciaFarmaciaes_ES
dc.subject.ecienciaMedicinaes_ES
dc.relation.publisherversionhttps://doi.org/10.18632/oncotarget.18948
dc.identifier.doi10.18632/oncotarget.18948
dc.identifier.publicationfirstpage67878es_ES
dc.identifier.publicationissue40es_ES
dc.identifier.publicationlastpage67890es_ES
dc.identifier.publicationvolume8es_ES
dc.relation.projectIDGobierno de España. SAF2014-56623-Res_ES
dc.type.versioninfo:eu-repo/semantics/publishedVersionen
dc.rights.ccReconocimientoes_ES
dc.rights.accessRightsopenAccesses_ES
dc.authorUAMBordas Sánchez , Anna (271716)
dc.authorUAMMontiel López, Carmen (259197)
dc.facultadUAMFacultad de Medicina
dc.institutoUAMInstituto de Investigación Sanitaria Hospital Universitario de La Paz (IdiPAZ)


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