Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/13757
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dc.contributor.authorYeo, Dannel-
dc.contributor.authorHuynh, Nhi-
dc.contributor.authorBeutler, John A-
dc.contributor.authorBaldwin, Graham S-
dc.contributor.authorHe, Hong-
dc.contributor.authorNikfarjam, Mehrdad-
dc.date2016-03-30-
dc.date.accessioned2016-04-06T01:04:14Z-
dc.date.accessioned2016-04-06T01:04:23Z-
dc.date.available2016-04-06T01:04:14Z-
dc.date.available2016-04-06T01:04:23Z-
dc.date.issued2016-12-
dc.identifier.citationJournal of Investigative Surgery 2016; 29(6): 366-372en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/13757-
dc.description.abstractBACKGROUND: Pancreatic cancer continues to have a poor survival rate with an urgent need for improved treatments. Glaucarubinone, a natural product first isolated from the seeds of the tree Simarouba glauca, has recently been recognized as having anti-cancer properties that may be particularly applicable to pancreatic cancer. METHODS: The effect of glaucarubinone on the growth and migration of murine pancreatic cancer cells was assessed by 3H-thymidine incorporation assay. The survival impact of glaucarubinone alone and in combination with gemcitabine chemotherapy was assessed using an immunocompetent orthotopic murine model of pancreatic cancer. RESULTS: Glaucarubinone inhibited the growth of the murine pancreatic cancer cell lines LM-P and PAN02. Treatment with either glaucarubinone or gemcitabine reduced proliferation in vitro and the combination was synergistic. The combination treatment improved survival two-fold compared to gemcitabine treatment alone (p = 0.046) in PAN02 cells. CONCLUSIONS: The synergistic inhibition by glaucarubinone and gemcitabine observed in vitro and the improved survival in vivo suggest that glaucarubinone may be a useful adjunct to current chemotherapy regimensen_US
dc.subjectGemcitabineen_US
dc.subjectGlaucarubinoneen_US
dc.subjectProstatic Neoplasmsen_US
dc.titleGlaucarubinone combined with gemcitabine improves pancreatic cancer survival in an immunocompetent orthotopic murine modelen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleJournal of Investigative Surgeryen_US
dc.identifier.affiliationDepartment of Surgery, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationMolecular Targets Laboratory, National Cancer Institute, Frederick, MD, USAen_US
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/27027695en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-0944-8747-
dc.identifier.orcid0000-0003-4866-276X-
dc.type.austinJournal Articleen_US
local.name.researcherHe, Hong
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptSurgery (University of Melbourne)-
crisitem.author.deptSurgery (University of Melbourne)-
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