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dc.contributor.authorGonzález Castrillón, Luz María-
dc.contributor.authorCock Rada, Alicia María-
dc.contributor.authorBohorquez Lozano, Mabel Elena-
dc.contributor.authorToa, Ted-
dc.contributor.authorEstrada Flórez, Ana Patricia-
dc.contributor.authorSuárez Olaya, John Jairo-
dc.contributor.authorBrea Fernández, Alejandro-
dc.contributor.authorCameselle Teijeiro, José-
dc.contributor.authorPinto, Carla-
dc.contributor.authorRamos, Irma-
dc.contributor.authorMantilla Morales, Alejandra-
dc.contributor.authorPrieto Sánchez, Rodrigo-
dc.contributor.authorCorvalán, Alejandro-
dc.contributor.authorNorero, Enrique-
dc.contributor.authorÁlvarez, Carolina-
dc.contributor.authorTapia, Teresa-
dc.contributor.authorCarvallo, Pilar-
dc.contributor.authorSahasrabudhe, Ruta-
dc.contributor.authorLott, Paul-
dc.contributor.authorSolano, Angela-
dc.contributor.authorNeffa, Florencia-
dc.contributor.authorDella Valle, Adriana-
dc.contributor.authorYau, Chris-
dc.contributor.authorSoares, Gabriela-
dc.contributor.authorBorowsky, Alexander-
dc.contributor.authorHu, Nan-
dc.contributor.authorHe, Li-Ji-
dc.contributor.authorHan, Xiao-You-
dc.contributor.authorTaylor, Philip R.-
dc.contributor.authorGoldstein, Alisa M.-
dc.contributor.authorTorres, Javier-
dc.contributor.authorEcheverry De Polanco, María Magdalena-
dc.contributor.authorRuiz Ponte, Clara-
dc.contributor.authorRodrigues Teixeira, Manuel António-
dc.contributor.authorCarvajal Carmona, Luis Guillermo-
dc.date.accessioned2023-03-14T22:53:31Z-
dc.date.available2023-03-14T22:53:31Z-
dc.date.issued2017-
dc.identifier.issn0016-5085-
dc.identifier.urihttps://hdl.handle.net/10495/34012-
dc.description.abstractABSTRACT: Up to 10% of cases of gastric cancer are familial, but so far, only mutations in CDH1 have been associated with gastric cancer risk. To identify genetic variants that affect risk for gastric cancer, we collected blood samples from 28 patients with hereditary diffuse gastric cancer (HDGC) not associated with mutations in CDH1 and performed whole-exome sequence analysis. We then analyzed sequences of candidate genes in 333 independent HDGC and non-HDGC cases. We identified 11 cases with mutations in PALB2 , BRCA1 , or RAD51C genes, which regulate homologous DNA recombination. We found these mutations in 2 of 31 patients with HDGC (6.5%) and 9 of 331 patients with sporadic gastric cancer (2.8%). Most of these mutations had been previously associated with other types of tumors and partially co-segregated with gastric cancer in our study. Tumors that developed in patients with these mutations had a mutation signature associated with somatic homologous recombination deficiency. Our findings indicate that defects in homologous recombination increase risk for gastric cancer.spa
dc.format.extent10 páginasspa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherWillians & Wilkinsspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.5/co/*
dc.titleGermline Mutations in PALB2, BRCA1, and RAD51C, wich Regulate DNA Recombination Repair, in Patients with Gastric Cancerspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupGenética Médicaspa
dc.identifier.doi10.1053/j.gastro.2016.12.010-
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn1528-0012-
oaire.citationtitleGastroenterologyspa
oaire.citationstartpage983spa
oaire.citationendpage986spa
oaire.citationvolume152spa
oaire.citationissue5spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by-nc-nd/4.0/spa
dc.publisher.placeBaltimore, Estados Unidosspa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsStomach-
dc.subject.decsEstómago-
dc.subject.decsStomach Neoplasms-
dc.subject.decsNeoplasias Gástricas-
dc.subject.decsWhole Exome Sequencing-
dc.subject.decsSecuenciación del Exoma Completo-
dc.subject.decsFanconi Anemia Complementation Group N Protein-
dc.subject.decsProteína del Grupo de Complementación N de la Anemia de Fanconi-
dc.subject.decsBRCA1 Protein-
dc.subject.decsProteína BRCA1-
dc.subject.decsRecombinational DNA Repair-
dc.subject.decsReparación del ADN por Recombinación-
dc.description.researchgroupidCOL0050839spa
dc.relation.ispartofjournalabbrevGastroenterologyspa
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