Publication:
Genetically Engineered Mouse Models of K-Ras-Driven Lung and Pancreatic Tumors: Validation of Therapeutic Targets

dc.contributor.authorDrosten, Matthias
dc.contributor.authorGuerra, Carmen
dc.contributor.authorBarbacid, Mariano
dc.contributor.funderUnión Europea. Comisión Europea. European Research Council (ERC)
dc.contributor.funderMinisterio de Economía y Competitividad (España)
dc.contributor.funderAsociación Española Contra el Cáncer
dc.date.accessioned2019-08-23T08:45:46Z
dc.date.available2019-08-23T08:45:46Z
dc.date.issued2018-05-01
dc.description.abstractK-RAS signaling has been intensely studied for over 40 years. Yet, as of today, no drugs have been approved to treat K-RAS mutant cancers. Since the turn of the century, scientists have used genetically engineered mouse (GEM) models to reproduce K-RAS mutant cancers in a laboratory setting to elucidate those molecular events responsible for the onset and progression of these tumors and to identify suitable therapies. In this review, we outline a brief description of available GEM models for two tumor types known to be driven by K-RAS mutations: lung adenocarcinoma and pancreatic ductal adenocarcinoma. In addition, we summarize a series of studies that have used these GEM tumor models to validate, either by genetic or pharmacological approaches, the therapeutic potential of a variety of targets, with the ultimate goal of translating these results to the clinical setting.es_ES
dc.description.peerreviewedes_ES
dc.description.sponsorshipThis work was supported by grants from the European Research Council (ERC-ADG/695566-THERACAN), the Spanish Ministry of Economy and Competitiveness (SAF2014-59864-R) and the Spanish Association against Cancer (AECC, GC16173694BARB).es_ES
dc.format.number5es_ES
dc.format.pagea031542es_ES
dc.format.volume8es_ES
dc.identifier.citationCold Spring Harb Perspect Med. 2018;8(5). pii: a031542.es_ES
dc.identifier.doi10.1101/cshperspect.a031542es_ES
dc.identifier.e-issn2157-1422es_ES
dc.identifier.issn2157-1422es_ES
dc.identifier.journalCold Spring Harbor perspectives in medicinees_ES
dc.identifier.pubmedID28778964es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/8313
dc.language.isoenges_ES
dc.publisherCold Spring Harbor Laboratory Press
dc.relation.projectIDinfo:eu-repo/grantAgreement/EC/H2020/695566es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/SAF2014-59864-Res_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/GC16173694BARBes_ES
dc.relation.publisherversionhttps://doi.org/ 10.1101/cshperspect.a031542.es_ES
dc.repisalud.institucionCNIOes_ES
dc.repisalud.orgCNIOCNIO::Grupos de investigación::Grupo de Oncología Experimentales_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución-NoComercial-CompartirIgual 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.subject.meshAnimalses_ES
dc.subject.meshGenes, rases_ES
dc.subject.meshMicees_ES
dc.subject.meshPharmacogeneticses_ES
dc.subject.meshSignal Transductiones_ES
dc.subject.meshAdenocarcinoma of Lunges_ES
dc.subject.meshCarcinoma, Pancreatic Ductales_ES
dc.subject.meshDisease Models, Animales_ES
dc.subject.meshLung Neoplasmses_ES
dc.subject.meshPancreatic Neoplasmses_ES
dc.titleGenetically Engineered Mouse Models of K-Ras-Driven Lung and Pancreatic Tumors: Validation of Therapeutic Targetses_ES
dc.typejournal articlees_ES
dc.type.hasVersionAMes_ES
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