Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/93440
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Type: Journal article
Title: Co-targeting AR and HSP90 suppresses prostate cancer cell growth and prevents resistance mechanisms
Author: Centenera, M.
Carter, S.
Gillis, J.
Marrocco-Tallarigo, D.
Grose, R.
Tilley, W.
Butler, L.
Citation: Endocrine-Related Cancer, 2015; 22(5):805-818
Publisher: BioScientifica
Issue Date: 2015
ISSN: 1351-0088
1479-6821
Statement of
Responsibility: 
Margaret M Centenera, Sarah L Carter, Joanna L Gillis, Deborah L Marrocco-Tallarigo, Randall H Grose, Wayne D Tilley and Lisa M Butler
Abstract: Persistent androgen receptor (AR) signaling in castration resistant prostate cancer (CRPC) underpins the urgent need for therapeutic strategies that better target this pathway. Combining classes of agents that target different components of AR signaling has the potential to delay resistance and improve patient outcomes. Many proto-oncogenes, including the AR, rely on the molecular chaperone heat shock protein 90 (Hsp90) for functional maturation and stability. In this study, enhanced anti-proliferative activity of the Hsp90 inhibitors 17-AAG and AUY922 in androgen-sensitive and castration-resistant prostate cancer cells was achieved when the agents were used in combination with AR antagonists bicalutamide or enzalutamide. Moreover, significant caspase-dependent cell death was achieved using sub-optimal agent doses that individually have no effect. Expression profiling demonstrated regulation of a broadened set of AR target genes with combined 17-AAG and bicalutamide compared with the respective single agent treatments. This enhanced inhibition of AR signaling was accompanied by impaired chromatin binding and AR nuclear localization. Importantly, expression of the AR variant AR-V7 that is implicated in resistance to AR antagonists was not induced by combination treatment. Likewise, the heat shock response that is typically elicited with therapeutic doses of Hsp90 inhibitors, and is a potential mediator of resistance to these agents, was significantly reduced by combination treatment. In summary, the co-targeting strategy in this study more effectively inhibits AR signaling than targeting AR or HSP90 alone and prevents induction of key resistance mechanisms in prostate cancer cells. These findings merit further evaluation of this therapeutic strategy to prevent CRPC growth.
Keywords: prostate cancer; heat shock protein; androgen receptor; combination
Rights: © 2015 by the Society for Endocrinology.
RMID: 0030032051
DOI: 10.1530/ERC-14-0541
Grant ID: http://purl.org/au-research/grants/nhmrc/453662
Appears in Collections:Medicine publications

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