Oncotarget

Research Papers:

Clusterin inhibition using OGX-011 synergistically enhances zoledronic acid activity in osteosarcoma

Francois Lamoureux _, Marc Baud’huin, Benjamin Ory, Romain Guiho, Amina Zoubeidi, Martin Gleave, Dominique Heymann & Françoise Rédini

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Oncotarget. 2014; 5:7805-7819. https://doi.org/10.18632/oncotarget.2308

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Abstract

Francois Lamoureux1,2,3,5, Marc Baud’huin1,2,3,4,5, Benjamin Ory1,2,3,5, Romain Guiho1,2,3,5, Amina Zoubeidi6, Martin Gleave6, Dominique Heymann1,2,3,4,5 and Françoise Rédini1,2,3,5

1 Université de Nantes, Nantes atlantique universités, Laboratoire de Physiopathologie de la Résorption Osseuse et Thérapie des Tumeurs Osseuses Primitives, Nantes F-44035, France 

2 INSERM, UMR 957, Nantes F-44035, France

3 LUNAM Université

4 CHU de Nantes, Nantes F-44035, France

5 Equipe labellisée LIGUE 2012, Nantes, cedex

6 The Vancouver Prostate Centre, University of British Columbia, Vancouver, BC, Canada

Correspondence:

François Lamoureux, email:

Françoise Rédini, email:

Keywords: zoledronic acid, clusterin, osteosarcoma, bone tumor

Received: April 24, 2014 Accepted: August 03, 2014 Published: August 04, 2014

Abstract

Purpose: Despite recent improvements in therapeutic management of osteosarcoma, ongoing challenges in improving the response to chemotherapy warrants new strategies still needed to improve overall patient survival. Among new therapeutic approaches, zoledronic acid (ZOL) represents a promising adjuvant molecule to chemotherapy to limit the osteolytic component of bone tumors. However, ZOL triggers the elevation of heat shock proteins (Hsp), including Hsp27 and clusterin (CLU), which could enhance tumor cell survival and treatment resistance. We hypothesized that targeting CLU using siRNA or the antisense drug, OGX-011, will suppress treatment-induced CLU induction and enhance ZOL-induced cell death in osteosarcoma (OS) cells.

Methods: The combined effects of OGX-011 and ZOL were investigated in vitro on cell growth, viability, apoptosis and cell cycle repartition of ZOL-sensitive or -resistant human OS cell lines (SaOS2, U2OS, MG63 and MNNG/HOS).

Results: In OS cell lines, ZOL increased levels of HSPs, especially CLU, in a dose- and time-dependent manner by mechanism including increased HSF1 transcription activity. The OS resistant cells to ZOL exhibited higher CLU expression level than the sensitive cells. Moreover, CLU overexpression protects OS sensitive cells to ZOL-induced cell death by modulating the MDR1 and farnesyl diphosphate synthase expression. OGX-011 suppressed treatment-induced increases in CLU and synergistically enhanced the activity of ZOL on cell growth and apoptosis. These biologic events were accompanied by decreased expression of HSPs, MDR1 and HSF1 transcriptional activity. In vivo, OGX-011, administered 3 times a week (IP, 20mg/kg), potentiated the effect of ZOL (s.c; 50µg/kg), significantly inhibiting tumor growth by 50% and prolonging survival in MNNG/HOS xenograft model compared to ZOL alone.

Conclusion: These results indicate that ZOL-mediated induction of CLU can be attenuated by OGX-011, with synergistic effects on delaying progression of osteosarcoma.


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