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dc.contributor.authorPickard, Rebecca D
dc.contributor.authorSpencer, Briohny H
dc.contributor.authorMcFarland, Amelia J
dc.contributor.authorBernaitis, Nijole
dc.contributor.authorDavey, Andrew K
dc.contributor.authorPerkins, Anthony V
dc.contributor.authorChess-Williams, Russ
dc.contributor.authorMcDermott, Catherine M
dc.contributor.authorForbes, Amanda
dc.contributor.authorChristie, David
dc.contributor.authorAnoopkumar-Dukie, Shailendra
dc.date.accessioned2018-01-04T02:25:10Z
dc.date.available2018-01-04T02:25:10Z
dc.date.issued2015
dc.identifier.issn0028-1298
dc.identifier.doi10.1007/s00210-015-1104-7
dc.identifier.urihttp://hdl.handle.net/10072/156055
dc.description.abstractDocetaxel was the first chemotherapeutic agent to increase survival time in patients with androgen-resistant prostate cancer. However, it provides only a modest increase in survival and is associated with significant toxicity. Therefore, there is an urgent need to identify potential adjunct therapies. Given the key role of autophagy in both tumour survival and chemoresistance, the impact of autophagy modulation on docetaxel toxicity was tested in vitro. PC-3 and LNCaP cells were pre-treated with the autophagy inhibitor 3-methyladenine (5 mM) and then exposed to various concentrations (0–100 μM) of docetaxel. Cytoxic effects of docetaxel were measured using resazurin reduction to resorufin, whilst autophagy and apoptosis was measured using monodansylcadaverine, annexin V and caspase-3, respectively. Docetaxel produced significant toxicity in PC-3 cells but was not toxic to LNCaP cells. Pre-treatment with the autophagy inhibitor, 3-methyladenine (5 mM) significantly protected PC-3 cells against docetaxel-induced cytotoxicity, increased autophagosome formation and apoptosis measured using monodansylcadaverine, annexin V and caspase-3 fluorescence, respectively. In contrast, 3-methyladenine was toxic by itself in LNCaP cells and also increased autophagic vesicle formation and apoptosis but did not influence docetaxel toxicity in these cells. These paradoxical effects of 3-methyladenine were largely independent of reactive oxygen species production. We show here that modulation of autophagy may influence docetaxel-induced toxicity in prostate cancer cells and these effects may differ between cell lines.
dc.description.peerreviewedYes
dc.languageEnglish
dc.publisherSpringer
dc.publisher.placeGermany
dc.relation.ispartofpagefrom793
dc.relation.ispartofpageto799
dc.relation.ispartofissue7
dc.relation.ispartofjournalNaunyn-Schmiedeberg's Archives of Pharmacology
dc.relation.ispartofvolume388
dc.subject.fieldofresearchPharmacology and Pharmaceutical Sciences not elsewhere classified
dc.subject.fieldofresearchPharmacology and Pharmaceutical Sciences
dc.subject.fieldofresearchcode111599
dc.subject.fieldofresearchcode1115
dc.titleParadoxical effects of the autophagy inhibitor 3-methyladenine on docetaxel-induced toxicity in PC-3 and LNCaP prostate cancer cells
dc.typeJournal article
dc.type.descriptionC1 - Articles
dc.type.codeC - Journal Articles
gro.hasfulltextNo Full Text
gro.griffith.authorPerkins, Anthony V.
gro.griffith.authorMcFarland, Amelia J.
gro.griffith.authorSpencer, Briohny H.
gro.griffith.authorAnoopkumar-Dukie, Shailendra
gro.griffith.authorPickard, Becky
gro.griffith.authorDavey, Andrew
gro.griffith.authorBernaitis, Nijole L.


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