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dc.contributor.authorEarl, Julie
dc.contributor.authorGalindo-Pumariño, Cristina
dc.contributor.authorEncinas, Jessica
dc.contributor.authorBarreto, Emma
dc.contributor.authorCastillo, Maria E
dc.contributor.authorPachón, Vanessa
dc.contributor.authorFerreiro, Reyes
dc.contributor.authorRodríguez-Garrote, Mercedes
dc.contributor.authorGonzález-Martínez, Silvia
dc.contributor.authorRamon Y Cajal, Teresa
dc.contributor.authorDiaz, Luis Robles
dc.contributor.authorChirivella-Gonzalez, Isabel
dc.contributor.authorRodríguez Pedreira, Monserrat
dc.contributor.authorde Castro, Eva Martínez
dc.contributor.authorGarcía-Seisdedos, David
dc.contributor.authorMuñoz, Gloria
dc.contributor.authorRosa, Juan Manuel Rosa
dc.contributor.authorMarquez, Mirari
dc.contributor.authorMalats, Nuría
dc.contributor.authorCarrato, Alfredo
dc.date.accessioned2022-03-17T08:18:18Z
dc.date.available2022-03-17T08:18:18Z
dc.date.issued2020
dc.identifier.issn2352-3964
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pubmed/32113160es
dc.identifier.urihttp://hdl.handle.net/20.500.11940/16292
dc.description.abstractBACKGROUND: The 5-year survival rate of patients with pancreatic ductal adenocarcinoma (PDAC) is around 5% due to the fact that the majority of patients present with advanced disease that is treatment resistant. Familial pancreatic cancer (FPC) is a rare disorder that is defined as a family with at least two affected first degree relatives, with an estimated incidence of 4%-10%. The genetic basis is unknown in the majority of families although around 10%-13% of families carry germline mutations in known genes associated with hereditary cancer and pancreatitis syndromes. METHODS: Panel sequencing was performed of 35 genes associated with hereditary cancer in 43 PDAC cases from families with an apparent hereditary pancreatic cancer syndrome. FINDINGS: Pathogenic variants were identified in 19% (5/26) of PDAC cases from pure FPC families in the genes MLH1, CDKN2A, POLQ and FANCM. Low frequency potentially pathogenic VUS were also identified in 35% (9/26) of PDAC cases from FPC families in the genes FANCC, MLH1, PMS2, CFTR, APC and MUTYH. Furthermore, an important proportion of PDAC cases harboured more than one pathogenic, likely pathogenic or potentially pathogenic VUS, highlighting the multigene phenotype of FPC. INTERPRETATION: The genetic basis of familial or hereditary pancreatic cancer can be explained in 21% of families by previously described hereditary cancer genes. Low frequency variants in other DNA repair genes are also present in 35% of families which may contribute to the risk of pancreatic cancer development. FUNDING: This study was funded by the Instituto de Salud Carlos III (Plan Estatal de I + D + i 2013-2016): ISCIII (PI09/02221, PI12/01635, PI15/02101 and PI18/1034) and co-financed by the European Development Regional Fund ''A way to achieve Europe'' (ERDF), the Biomedical Research Network in Cancer: CIBERONC (CB16/12/00446), Red Tematica de investigacion cooperativa en cancer: RTICC (RD12/0036/0073) and La Asociacion Espanola contra el Cancer: AECC (Grupos Coordinados Estables 2016).en
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.meshAdult*
dc.subject.meshMutation Rate*
dc.subject.meshMiddle Aged*
dc.subject.meshHumans*
dc.subject.meshDNA Helicases*
dc.subject.meshPancreatic Neoplasms*
dc.subject.meshPedigree*
dc.subject.meshCyclin-Dependent Kinase Inhibitor p16*
dc.subject.meshAdenocarcinoma*
dc.subject.meshAged*
dc.subject.meshDNA-Directed DNA Polymerase*
dc.titleA comprehensive analysis of candidate genes in familial pancreatic cancer families reveals a high frequency of potentially pathogenic germline variantsen
dc.typeJournal Articlees
dc.authorsophosEarl, Julie;Galindo-Pumariño, Cristina;Encinas, Jessica;Barreto, Emma;Castillo, Maria E;Pachón, Vanessa;Ferreiro, Reyes;Rodríguez-Garrote, Mercedes;González-Martínez, Silvia;Ramon Y Cajal, Teresa;Diaz, Luis Robles;Chirivella-Gonzalez, Isabel;Rodriguez, Montse;de Castro, Eva Martínez;García-Seisdedos, David;Muñoz, Gloria;Rosa, Juan Manuel Rosa;Marquez, Mirari;Malats, Nuría;Carrato, Alfredo
dc.identifier.doi10.1016/j.ebiom.2020.102675
dc.identifier.pmid32113160
dc.identifier.sophos36272
dc.journal.titleEBioMedicinees
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de A Coruña - Complexo Hospitalario Universitario de A Coruña::Dixestivoes
dc.rights.accessRightsopenAccess
dc.subject.decstasa de mutación*
dc.subject.decsanciano*
dc.subject.decsinhibidor p16 de cinasas dependientes de ciclinas*
dc.subject.decsneoplasias pancreáticas*
dc.subject.decsmediana edad*
dc.subject.decshumanos*
dc.subject.decslinaje*
dc.subject.decsADN helicasas*
dc.subject.decsadulto*
dc.subject.decsADN polimerasa dirigida por ADN*
dc.subject.decsadenocarcinoma*
dc.subject.keywordCHUACes
dc.typefidesArtículo Originales
dc.typesophosArtículo Originales
dc.volume.number53.es


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