Department of Urology, Kyoto University Graduate School of Medicine, Kyoto 606-8507, Japan.
Cancer Res. 2010 Feb 15;70(4):1606-15. doi: 10.1158/0008-5472.CAN-09-2984. Epub 2010 Feb 9.
More effective therapeutic approaches for castration-resistant prostate cancer (CRPC) are urgently needed, thus reinforcing the need to understand how prostate tumors progress to castration resistance. We have established a novel mouse xenograft model of prostate cancer, KUCaP-2, which expresses the wild-type androgen receptor (AR) and which produces the prostate-specific antigen (PSA). In this model, tumors regress soon after castration, but then reproducibly restore their ability to proliferate after 1 to 2 months without AR mutation, mimicking the clinical behavior of CRPC. In the present study, we used this model to identify novel therapeutic targets for CRPC. Evaluating tumor tissues at various stages by gene expression profiling, we discovered that the prostaglandin E receptor EP4 subtype (EP4) was significantly upregulated during progression to castration resistance. Immunohistochemical results of human prostate cancer tissues confirmed that EP4 expression was higher in CRPC compared with hormone-naïve prostate cancer. Ectopic overexpression of EP4 in LNCaP cells (LNCaP-EP4 cells) drove proliferation and PSA production in the absence of androgen supplementation in vitro and in vivo. Androgen-independent proliferation of LNCaP-EP4 cells was suppressed when AR expression was attenuated by RNA interference. Treatment of LNCaP-EP4 cells with a specific EP4 antagonist, ONO-AE3-208, decreased intracellular cyclic AMP levels, suppressed PSA production in vitro, and inhibited castration-resistant growth of LNCaP-EP4 or KUCaP-2 tumors in vivo. Our findings reveal that EP4 overexpression, via AR activation, supports an important mechanism for castration-resistant progression of prostate cancer. Furthermore, they prompt further evaluation of EP4 antagonists as a novel therapeutic modality to treat CRPC.
更有效的治疗方法迫切需要去治疗去势抵抗性前列腺癌(CRPC),因此需要了解前列腺肿瘤如何进展为去势抵抗。我们建立了一个新的前列腺癌小鼠异种移植模型,KUCaP-2,它表达野生型雄激素受体(AR),并产生前列腺特异性抗原(PSA)。在这个模型中,肿瘤在去势后很快消退,但在没有 AR 突变的情况下,1 到 2 个月后可重现地恢复其增殖能力,模拟 CRPC 的临床行为。在本研究中,我们使用该模型来鉴定 CRPC 的新治疗靶点。通过基因表达谱分析评估不同阶段的肿瘤组织,我们发现前列腺素 E 受体 EP4 亚型(EP4)在向去势抵抗进展过程中显著上调。人前列腺癌组织的免疫组织化学结果证实,与激素-naïve 前列腺癌相比,CRPC 中 EP4 的表达更高。在 LNCaP 细胞(LNCaP-EP4 细胞)中外源过表达 EP4,在没有雄激素补充的情况下,在体外和体内驱动增殖和 PSA 产生。当 AR 表达通过 RNA 干扰减弱时,LNCaP-EP4 细胞的雄激素非依赖性增殖受到抑制。用特异性 EP4 拮抗剂 ONO-AE3-208 处理 LNCaP-EP4 细胞,降低细胞内环腺苷酸水平,体外抑制 PSA 产生,并抑制体内 LNCaP-EP4 或 KUCaP-2 肿瘤的去势抵抗生长。我们的发现表明,EP4 通过 AR 激活的过表达,支持了前列腺癌去势抵抗进展的一个重要机制。此外,它们促使进一步评估 EP4 拮抗剂作为治疗 CRPC 的一种新的治疗方式。