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Please use this identifier to cite or link to this item: http://hdl.handle.net/2067/51565
DC FieldValueLanguage
dc.contributor.authorMarengo, Alessandroit
dc.contributor.authorForciniti, Stefaniait
dc.contributor.authorDando, Ilariait
dc.contributor.authorDalla Pozza, Elisait
dc.contributor.authorStella, Barbarait
dc.contributor.authorTsapis, Nicolasit
dc.contributor.authorYagoubi, Najetit
dc.contributor.authorFanelli, Giuseppinait
dc.contributor.authorFattal, Eliasit
dc.contributor.authorHeeschen, Christopherit
dc.contributor.authorPalmieri, Martait
dc.contributor.authorArpicco, Silviait
dc.date.accessioned2024-07-23T07:55:13Z-
dc.date.available2024-07-23T07:55:13Z-
dc.date.issued2019it
dc.identifier.issn0304-4165it
dc.identifier.urihttp://hdl.handle.net/2067/51565-
dc.description.abstractPancreatic cancer stem cells (CSCs) are responsible for resistance to standard therapy, metastatic potential, and disease relapse following treatments. The current therapy for pancreatic ductal adenocarcinoma (PDAC) preferentially targets the more differentiated cancer cell population, leaving CSCs as a cell source for tumor mass formation and recurrence. For this reason, there is an urgent need to improve current therapies and develop novel CSC-targeted therapeutic approaches.it
dc.language.isoengit
dc.rightsAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titlePancreatic cancer stem cell proliferation is strongly inhibited by diethyldithiocarbamate-copper complex loaded into hyaluronic acid decorated liposomesit
dc.typearticle*
dc.identifier.doi10.1016/j.bbagen.2018.09.018it
dc.identifier.pmid30267751it
dc.identifier.scopuss2.0-85047862536&it
dc.identifier.urlwww.elsevier.com/locate/bbagenit
dc.relation.journalBIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTSit
dc.relation.firstpage61it
dc.relation.lastpage72it
dc.relation.volume1863it
dc.relation.issue1it
dc.subject.keywordsCD44; Diethyldithiocarbamate/copper complex; Hyaluronic acid; Liposomes; Pancreatic cancer stem cells; PDAC patient-derived cells; Biophysics; Biochemistry; Molecular Biologyit
dc.description.numberofauthors12it
dc.type.refereeREF_1it
dc.type.miur262*
item.fulltextWith Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
item.grantfulltextrestricted-
item.openairetypearticle-
item.cerifentitytypePublications-
crisitem.journal.journalissn0304-4165-
crisitem.journal.anceE022079-
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