Figure 4 from Attenuating Adaptive VEGF-A and IL8 Signaling Restores Durable Tumor Control in AR Antagonist–Treated Prostate Cancers
Maxwell PJ., McKechnie M., Armstrong CW., Manley JM., Ong CW., Worthington J., Mills IG., Longley DB., Quigley JP., Zoubeidi A., de Bono JS., Deryugina E., LaBonte MJ., Waugh DJJ.
VEGF and IL8 expression is altered and plays a role in resistance in enzalutamide-resistant prostate cancer cell lines. Cells were treated with anti-IL8 nAb (5 μg/mL), anti-VEGF nAb (10 μg/mL), or the highest concentration of isotype-matched human IgG antibody. A, qRT-PCR data comparing basal expression of VEGFA and CXCL8 (IL8) expression in LNCaP-Parental (PAR), LNCaP-EnzR, CWR-R1-Par, and CWR-R1-EnzR cell lines. B, ELISA data comparing basal secretion of VEGF and IL8 in LNCaP-Par, LNCaP-EnzR, CWR-R1-Par, and CWR-R1-EnzR cells. Data shown are the mean±SEM of N = 4 experiments. C–F, Bar graphs demonstrating the effect of combined treatment with anti-IL8 nAb and anti-VEGF nAb on the response of LNCaP-Par, LNCaP-EnzR, CWR-R1-Par, and CWR-R1-EnzR cells to 10 μmol/L Enz over 72 hours in (C and D) normoxia and (E and F) hypoxia. All experiments data represented as the mean ± SEM of N = 3 experiments, unless otherwise stated and statistical analysis was carried out using a Mann-Whitney U test: *, P < 0.05; **, P < 0.01.

