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dc.creatorSereti E., Karagianellou T., Kotsoni I., Magouliotis D., Kamposioras K., Ulukaya E., Sakellaridis N., Zacharoulis D., Dimas K.en
dc.date.accessioned2023-01-31T09:55:06Z
dc.date.available2023-01-31T09:55:06Z
dc.date.issued2018
dc.identifier10.1016/j.jprot.2018.01.012
dc.identifier.issn18743919
dc.identifier.urihttp://hdl.handle.net/11615/78895
dc.description.abstractThe prognosis of pancreatic ductal adenocarcinoma (PDAC), the eighth most lethal cancer for men and ninth for women worldwide, remains dismal. The increasing rates of deaths by PDAC indicate that the overall management of the disease in 21st century is still insufficient. Thus it is obvious that there is an unmet need to improve management of PDAC by finding new biomarkers to screen high risk patients, confirm diagnosis, and predict response to treatment as well more efficacious and safer treatments. Patient Derived Xenografts (PDX) have been developed as a new promising tool in an effort to mirror genetics, tumor heterogeneity and cancer microenvironment of the primary tumor. Herein we aim to give an updated overview of the current status and the perspectives of PDX in the search for the identification of novel biomarkers and improved therapeutic outcomes for PDAC but also their use as a valuable tool towards individualized treatments to improve the outcome of the disease. Furthermore, we critically review the applications, advantages, limitations, and perspectives of PDX in the research towards an improved management of PDAC. Significance: This review provides a comprehensive overview of the current status and the potential role as well as the challenges of PDX in the road to fight one of the most lethal cancers in the developed countries, pancreatic ductal adenocarcinoma. © 2018 Elsevier B.V.en
dc.language.isoenen
dc.sourceJournal of Proteomicsen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85041597885&doi=10.1016%2fj.jprot.2018.01.012&partnerID=40&md5=c3c7d85748436908ab65dcfd3fd010c3
dc.subjectantineoplastic agenten
dc.subjectbiological markeren
dc.subjectheat shock protein 90en
dc.subjecttumor markeren
dc.subjectArticleen
dc.subjectcancer cell lineen
dc.subjectcancer prognosisen
dc.subjectcancer stem cellen
dc.subjectcorrelation analysisen
dc.subjectdeveloped countryen
dc.subjectdrug researchen
dc.subjecthigh risk patienten
dc.subjecthumanen
dc.subjectmethodologyen
dc.subjectnonhumanen
dc.subjectoncogeneen
dc.subjectpancreas adenocarcinomaen
dc.subjectpatient derived xenograften
dc.subjectpersonalized medicineen
dc.subjectprimary tumoren
dc.subjectpriority journalen
dc.subjecttreatment outcomeen
dc.subjecttumor microenvironmenten
dc.subjecttumor xenograften
dc.subjectanimalen
dc.subjectdrug developmenten
dc.subjectpancreas carcinomaen
dc.subjectpathologyen
dc.subjectpersonalized medicineen
dc.subjectproceduresen
dc.subjectxenograften
dc.subjectAnimalsen
dc.subjectBiomarkers, Tumoren
dc.subjectCarcinoma, Pancreatic Ductalen
dc.subjectDrug Discoveryen
dc.subjectHeterograftsen
dc.subjectHumansen
dc.subjectPrecision Medicineen
dc.subjectElsevier B.V.en
dc.titlePatient Derived Xenografts (PDX) for personalized treatment of pancreatic cancer: emerging allies in the war on a devastating cancer?en
dc.typejournalArticleen


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