Abstract A087: Enzalutamide-induced hypoxia attenuates response and promotes resistance to enzalutamide in preclinical models of prostate cancer

• Published in: Cancer research (Chicago, Ill.) Ill.), 2018-08, Vol.78 (16_Supplement), p.A087-A087
• Main Authors: Maxwell, Pamela J., McKechnie, Melanie, Duddy, Oisin, Armstrong, Christopher W., Manley, Judith M., Ong, Chee Wee, Worthington, Jenny, Deryugina, Elena, Quigley, James P., Zoubeidi, Amina, Waugh, David J.J., LaBonte, Melissa J.
• Format: Article
• Language: eng ; jpn
• ISSN: 0008-5472; 1538-7445
• DOI: 10.1158/1538-7445.PRCA2017-A087

Inhibition of androgen signaling remains the therapeutic mainstay in castrate-resistant prostate cancer. The expression of androgen receptor (AR) splice variants and the retention of active AR signaling have been reported as mechanisms of resistance to the anti-androgen enzalutamide. Other non-AR dependent mechanisms of resistance have also been proposed, including acquisition of a hypoxic tumor microenvironment. We propose that treatment-induced hypoxia and the subsequent induction of angiogenesis may define a novel mechanism of relapse to enzalutamide. Preclinical experiments were conducted in LNCaP tumors, endothelial cells, and established human prostate cancer cell lines. The effects of enzalutamide on endothelial cells were examined in vivo and in vitro. Tumor growth, intratumoral hypoxia, and blood vessel density were measured in vivo. AR expression, activation, and target gene expression were measured in vitro. The effect of enzalutamide on hypoxia-driven, disease-progressing pathways and genes of interest, and the role of these genes in resistance to enzalutamide, was investigated. Administration of enzalutamide rapidly induced hypoxia in LNCaP tumors in vivo, followed by angiogenesis-promoted restoration of oxygen tension, increased vessel density, and accelerated tumor growth. In vitro, enzalutamide directly targeted AR-expressing endothelial cells, resulting in decreased growth and tubule formation. Exposure to hypoxia in vitro increased AR expression and transcriptional activity in LNCaP prostate cancer cells and sustained, but did not further potentiate, high basal AR and ARv7 expression and activity in 22Rv1 cells. Enzalutamide failed to attenuate the concurrent hypoxia-induced HIF-1 and NF-κB signaling, resulting in upregulation of disease-progressing genes and pathways. Administration of neutralizing antibodies to two hypoxia-regulated genes, interleukin-8 (IL-8) and VEGF, prolonged enzalutamide-mediated hypoxia over 14 days and LNCaP tumor growth control over 28 days in vivo (p