Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/50283
Full metadata record
DC FieldValueLanguage
dc.contributor.authorPérez Torras, Sandra-
dc.contributor.authorVidal Pla, Anna-
dc.contributor.authorMiquel Morera, Rosa-
dc.contributor.authorAlmendro Navarro, Vanessa-
dc.contributor.authorFernández-Cruz, Laureano-
dc.contributor.authorNavarro Colás, Salvador-
dc.contributor.authorMaurel Santasusana, Joan-
dc.contributor.authorCarbó Carbó, Neus-
dc.contributor.authorGascón, Pere-
dc.contributor.authorMazo Sánchez, Adela-
dc.date.accessioned2014-02-18T13:28:58Z-
dc.date.available2014-02-18T13:28:58Z-
dc.date.issued2011-11-01-
dc.identifier.issn1570-5870-
dc.identifier.urihttp://hdl.handle.net/2445/50283-
dc.description.abstractBackground Efforts to identify novel therapeutic options for human pancreatic ductal adenocarcinoma (PDAC) have failed to result in a clear improvement in patient survival to date. Pancreatic cancer requires efficient therapies that must be designed and assayed in preclinical models with improved predictor ability. Among the available preclinical models, the orthotopic approach fits with this expectation, but its use is still occasional. Methods An in vivo platform of 11 orthotopic tumor xenografts has been generated by direct implantation of fresh surgical material. In addition, a frozen tumorgraft bank has been created, ensuring future model recovery and tumor tissue availability. Results Tissue microarray studies allow showing a high degree of original histology preservation and maintenance of protein expression patterns through passages. The models display stable growth kinetics and characteristic metastatic behavior. Moreover, the molecular diversity may facilitate the identification of tumor subtypes and comparison of drug responses that complement or confirm information obtained with other preclinical models. Conclusions This panel represents a useful preclinical tool for testing new agents and treatment protocols and for further exploration of the biological basis of drug responses.-
dc.format.extent11 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherIOS Press-
dc.relation.isformatofReproducció del document publicat a: http://dx.doi.org/10.1007/s13402-011-0049-1-
dc.relation.ispartofAnalytical Cellular Pathology / Cellular Oncology, 2011, vol. 34, num. 6, p. 511-521-
dc.relation.urihttp://dx.doi.org/10.1007/s13402-011-0049-1-
dc.rights(c) IOS Press, 2011-
dc.sourceArticles publicats en revistes (Bioquímica i Biomedicina Molecular)-
dc.subject.classificationCàncer-
dc.subject.classificationPàncrees-
dc.subject.classificationGenètica molecular-
dc.subject.classificationTeràpia genètica-
dc.subject.otherCancer-
dc.subject.otherPancreas-
dc.subject.otherMolecular genetics-
dc.subject.otherGene therapy-
dc.titleCharacterization of human pancreatic orthotopic tumor xenografts suitable for drug screeningeng
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec625113-
dc.date.updated2014-02-18T13:28:59Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid21681527-
Appears in Collections:Articles publicats en revistes (Bioquímica i Biomedicina Molecular)
Articles publicats en revistes (Medicina)

Files in This Item:
File Description SizeFormat 
625113.pdf907.53 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.