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dc.contributor.authorCasal-Mouriño, A.
dc.contributor.authorRuano-Ravina, A.
dc.contributor.authorTorres Durán, María Luisa 
dc.contributor.authorParente Lamelas, Isaura 
dc.contributor.authorProvencio-Pulla, M.
dc.contributor.authorCastro Añon, Olalla 
dc.contributor.authorVidal-García, I.
dc.contributor.authorAbal-Arca, J.
dc.contributor.authorPiñeiro-Lamas, M.
dc.contributor.authorFernández Villar, José Alberto 
dc.contributor.authorValdés-Cuadrado, L.
dc.contributor.authorBarros-Dios, J. M.
dc.contributor.authorPérez-Ríos, M.
dc.date.accessioned2022-05-19T08:33:24Z
dc.date.available2022-05-19T08:33:24Z
dc.date.issued2020
dc.identifier.issn2045-2322
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pubmed/33273562es
dc.identifier.urihttp://hdl.handle.net/20.500.11940/16740
dc.description.abstractPolymorphisms in DNA repair pathways may play a relevant role in lung cancer survival in never-smokers. Furthermore, they could be implicated in the response to chemotherapy and toxicity of platinum agents. The aim of this study was to evaluate the influence of various genetic polymorphisms in the BER and NER DNA repair pathways on survival and toxicity in never-smoker LC patients. The study included never-smokers LC cases diagnosed from 2011 through 2019, belonging to the Lung Cancer Research In Never Smokers study. A total of 356 never-smokers cases participated (79% women; 83% adenocarcinoma and 65% stage IV). Survival at 3 and 5 years from diagnosis was not associated with genetic polymorphisms, except in the subgroup of patients who received radiotherapy or chemo-radiotherapy, and presented with ERCC1 rs3212986 polymorphism. There was greater toxicity in those presenting OGG1 rs1052133 (CG) and ERCC1 rs11615 polymorphisms among patients treated with radiotherapy or chemo-radiotherapy, respectively. In general, polymorphisms in the BER and NER pathways do not seem to play a relevant role in survival and response to treatment among never-smoker LC patients.en
dc.rightsAtribución 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.meshSurvival Analysis*
dc.subject.meshLung Neoplasms*
dc.subject.meshMiddle Aged*
dc.subject.meshHumans*
dc.subject.meshCase-Control Studies*
dc.subject.meshAged*
dc.titlePolymorphisms in the BER and NER pathways and their influence on survival and toxicity in never-smokers with lung canceren
dc.typeJournal Articlees
dc.authorsophosCasal-Mouriño, A.;Ruano-Ravina, A.;Torres-Durán, M.;Parente-Lamelas, I.;Provencio-Pulla, M.;Castro-Añón, O.;Vidal-García, I.;Abal-Arca, J.;Piñeiro-Lamas, M.;Fernández-Villar, A.;Valdés-Cuadrado, L.;Barros-Dios, J. M.;Pérez-Ríos, M.
dc.identifier.doi10.1038/s41598-020-78051-5
dc.identifier.pmid33273562
dc.identifier.sophos40467
dc.issue.number1es
dc.journal.titleScientific Reportses
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Ourense, Verín e O Barco de Valdeorras - Complexo Hospitalario Universitario de Ourense::Neumoloxíaes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Vigo - Complexo Hospitalario Universitario de Vigo::Neumoloxíaes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de Lugo, Cervo e Monforte de lemos - Complexo Hospitalario Universitario Lucus Augusti::Neumoloxíaes
dc.page.initial21147es
dc.rights.accessRightsopenAccess
dc.subject.decsestudios de casos y controles*
dc.subject.decsanciano*
dc.subject.decsmediana edad*
dc.subject.decshumanos*
dc.subject.decsanálisis de supervivencia*
dc.subject.decsneoplasias pulmonares*
dc.subject.keywordCHUOes
dc.subject.keywordCHUVIes
dc.subject.keywordHULAes
dc.typefidesArtículo Originales
dc.typesophosArtículo Originales
dc.volume.number10es


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