VA Northern California Health Care System, Mather, California, USA.
Cancer Res. 2010 Jul 15;70(14):5994-6003. doi: 10.1158/0008-5472.CAN-09-4440. Epub 2010 Jun 29.
Patients with advanced prostate cancer (PCa) are initially susceptible to androgen withdrawal (AW), but ultimately develop resistance to this therapy (castration-resistant PCa, CRPC). Here, we show that AW can promote CRPC development by increasing the levels of the receptor tyrosine kinase ErbB3 in androgen-dependent PCa, resulting in AW-resistant cell cycle progression and increased androgen receptor (AR) transcriptional activity. CRPC cell lines and human PCa tissue overexpressed ErbB3, whereas downregulation of ErbB3 prevented CRPC cell growth. Investigation of the mechanism by which AW augments ErbB3, using normal prostate-derived pRNS-1-1 cells, and androgen-dependent PCa lines LNCaP, PC346C, and CWR22 mouse xenografts, revealed that the AR suppresses ErbB3 protein levels, whereas AW relieves this suppression, showing for the first time the negative regulation of ErbB3 by AR. We show that AR activation promotes ErbB3 degradation in androgen-dependent cells, and that this effect is mediated by AR-dependent transcriptional upregulation of neuregulin receptor degradation protein-1 (Nrdp1), an E3 ubiquitin ligase that targets ErbB3 for degradation but whose role in PCa has not been previously examined. Therefore, AW decreases Nrdp1 expression, promoting ErbB3 protein accumulation, and leading to AR-independent proliferation. However, in CRPC sublines of LNCaP and CWR22, which strongly overexpress the AR, ErbB3 levels remain elevated due to constitutive suppression of Nrdp1, which prevents AR regulation of Nrdp1. Our observations point to a model of CRPC development in which progression of PCa to castration resistance is associated with the inability of AR to transcriptionally regulate Nrdp1, and predict that inhibition of ErbB3 during AW may impair CRPC development.
患有晚期前列腺癌 (PCa) 的患者最初对雄激素剥夺 (AW) 敏感,但最终对这种治疗产生耐药性(去势抵抗性 PCa,CRPC)。在这里,我们表明,AW 通过增加雄激素依赖性 PCa 中受体酪氨酸激酶 ErbB3 的水平来促进 CRPC 的发展,导致 AW 抵抗的细胞周期进展和增加的雄激素受体 (AR) 转录活性。CRPC 细胞系和人前列腺癌组织过度表达 ErbB3,而 ErbB3 的下调则阻止了 CRPC 细胞的生长。使用正常前列腺衍生的 pRNS-1-1 细胞和雄激素依赖性 PCa 系 LNCaP、PC346C 和 CWR22 小鼠异种移植,研究 AW 增强 ErbB3 的机制,发现 AR 抑制 ErbB3 蛋白水平,而 AW 解除这种抑制,首次显示 AR 对 ErbB3 的负调节作用。我们表明,AR 激活促进雄激素依赖性细胞中 ErbB3 的降解,并且这种作用是通过 AR 依赖性转录上调神经调节蛋白受体降解蛋白 1 (Nrdp1) 介导的,Nrdp1 是一种 E3 泛素连接酶,可靶向 ErbB3 进行降解,但在之前的 PCa 研究中尚未对其作用进行研究。因此,AW 降低 Nrdp1 的表达,促进 ErbB3 蛋白积累,导致 AR 非依赖性增殖。然而,在 LNCaP 和 CWR22 的 CRPC 亚系中,由于 Nrdp1 的组成性抑制,AR 强烈过表达,ErbB3 水平仍然升高,这阻止了 AR 对 Nrdp1 的调节。我们的观察结果指出了一种 CRPC 发展模型,其中 PCa 进展为去势抵抗与 AR 无法转录调节 Nrdp1 有关,并预测在 AW 期间抑制 ErbB3 可能会损害 CRPC 的发展。