Omics approaches in pancreatic adenocarcinoma

dc.contributor.authorGonzález Borja, Iranzu
dc.contributor.authorViúdez, Antonio
dc.contributor.authorGoñi Irigoyen, Saioa
dc.contributor.authorSantamaría Martínez, Enrique
dc.contributor.authorCarrasco García, Estefanía
dc.contributor.authorPérez Sanz, Jairo
dc.contributor.authorHernández García, Irene
dc.contributor.departmentCiencias de la Saludes_ES
dc.contributor.departmentOsasun Zientziakeu
dc.contributor.funderGobierno de Navarra / Nafarroako Gobernua, Ref. 008-2018es
dc.date.accessioned2020-02-18T13:10:05Z
dc.date.available2020-02-18T13:10:05Z
dc.date.issued2019
dc.description.abstractPancreatic ductal adenocarcinoma, which represents 80% of pancreatic cancers, is mainly diagnosed when treatment with curative intent is not possible. Consequently, the overall five-year survival rate is extremely dismal—around 5% to 7%. In addition, pancreatic cancer is expected to become the second leading cause of cancer-related death by 2030. Therefore, advances in screening, prevention and treatment are urgently needed. Fortunately, a wide range of approaches could help shed light in this area. Beyond the use of cytological or histological samples focusing in diagnosis, a plethora of new approaches are currently being used for a deeper characterization of pancreatic ductal adenocarcinoma, including genetic, epigenetic, and/or proteo-transcriptomic techniques. Accordingly, the development of new analytical technologies using body fluids (blood, bile, urine, etc.) to analyze tumor derived molecules has become a priority in pancreatic ductal adenocarcinoma due to the hard accessibility to tumor samples. These types of technologies will lead us to improve the outcome of pancreatic ductal adenocarcinoma patients.en
dc.description.sponsorshipThis work was funded by grants from Department of Health from Government of Navarra (Ref. 008-2018), REFBIO II Pyrenees Biomedical Network from Programa INTERREG V-A España-Francia-Andora (Ref. BMK_PANC) and Sociedad Española de Oncología Médica (SEOM) to A.V. I.G.-B. is supported by a predoctoral fellowship from Department of Economic Development Government of Navarre 'Ayudas para la contratación de doctorandos y doctorandas por empresas y organismos de investigación y difusión de conocimientos: doctorados industriales 2018–2020'.en
dc.format.extent19 p.
dc.format.mimetypeapplication/pdfen
dc.identifier.doi10.3390/cancers11081052
dc.identifier.issn2072-6694
dc.identifier.urihttps://academica-e.unavarra.es/handle/2454/36276
dc.language.isoengen
dc.publisherMDPIen
dc.relation.ispartofCancers, 2019, 11 (8), 1052en
dc.relation.publisherversionhttps://doi.org/10.3390/cancers11081052
dc.rights© 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.en
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectPancreatic adenocarcinomaen
dc.subjectCtDNAen
dc.subjectProteomicen
dc.subjectGenomicen
dc.subjectMetabolomicen
dc.subjectLipidomicen
dc.subjectFFPEen
dc.subjectTissueen
dc.subjectBody fluidsen
dc.titleOmics approaches in pancreatic adenocarcinomaen
dc.typeinfo:eu-repo/semantics/article
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dspace.entity.typePublication
relation.isAuthorOfPublication7945ddd5-cf8b-4927-bd7a-4ade2fb61f11
relation.isAuthorOfPublicationabacfd17-2b93-4d99-bae2-52053d57401e
relation.isAuthorOfPublication.latestForDiscovery7945ddd5-cf8b-4927-bd7a-4ade2fb61f11

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