Characterization of human pancreatic orthotopic tumor xenografts suitable for drug screening

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.date.updated2014-02-18T13:28:59Z
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.identifier.idgrec625113
dc.identifier.issn1570-5870
dc.identifier.pmid21681527
dc.identifier.urihttps://hdl.handle.net/2445/50283
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.rights.accessRightsinfo:eu-repo/semantics/openAccess
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

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