Department of Molecular Medicine, UT Health San Antonio, San Antonio, Texas.
Department of Cell Systems & Anatomy, UT Health San Antonio, San Antonio, Texas.
Mol Cancer Res. 2022 Jan;20(1):62-76. doi: 10.1158/1541-7786.MCR-21-0108. Epub 2021 Oct 5.
Although the Sonic hedgehog (SHH) signaling pathway has been implicated in promoting malignant phenotypes of prostate cancer, details on how it is activated and exerts its oncogenic role during prostate cancer development and progression is less clear. Here, we show that GLI3, a key SHH pathway effector, is transcriptionally upregulated during androgen deprivation and posttranslationally stabilized in prostate cancer cells by mutation of speckle-type POZ protein (SPOP). GLI3 is a substrate of SPOP-mediated proteasomal degradation in prostate cancer cells and prostate cancer driver mutations in SPOP abrogate GLI3 degradation. Functionally, GLI3 is necessary and sufficient for the growth and migration of androgen receptor (AR)-positive prostate cancer cells, particularly under androgen-depleted conditions. Importantly, we demonstrate that GLI3 physically interacts and functionally cooperates with AR to enrich an AR-dependent gene expression program leading to castration-resistant growth of xenografted prostate tumors. Finally, we identify an AR/GLI3 coregulated gene signature that is highly correlated with castration-resistant metastatic prostate cancer and predictive of disease recurrence. Together, these findings reveal that hyperactivated GLI3 promotes castration-resistant growth of prostate cancer and provide a rationale for therapeutic targeting of GLI3 in patients with castration-resistant prostate cancer (CRPC). IMPLICATIONS: We describe two clinically relevant mechanisms leading to hyperactivated GLI3 signaling and enhanced AR/GLI3 cross-talk, suggesting that GLI3-specific inhibitors might prove effective to block prostate cancer development or delay CRPC.
尽管 Sonic hedgehog (SHH) 信号通路被认为能促进前列腺癌的恶性表型,但它在前列腺癌发生和发展过程中如何被激活以及发挥致癌作用的细节尚不清楚。在这里,我们表明,Sonic hedgehog (SHH) 信号通路的关键效应物 GLI3 在雄激素剥夺期间转录上调,并通过 speckle-type POZ protein (SPOP) 突变在前列腺癌细胞中被翻译后稳定。GLI3 是 SPOP 介导的前列腺癌细胞中蛋白酶体降解的底物,并且 SPOP 中的前列腺癌驱动突变会消除 GLI3 的降解。功能上,GLI3 对于雄激素受体 (AR) 阳性前列腺癌细胞的生长和迁移是必需的和充分的,特别是在雄激素耗尽的情况下。重要的是,我们证明了 GLI3 与 AR 物理相互作用并协同作用,以富集依赖 AR 的基因表达程序,导致异种移植前列腺肿瘤的去势抵抗生长。最后,我们确定了一个 AR/GLI3 共同调节的基因特征,该特征与去势抵抗转移性前列腺癌高度相关,并可预测疾病复发。总之,这些发现表明,过度激活的 GLI3 促进了前列腺癌的去势抵抗生长,并为针对去势抵抗前列腺癌 (CRPC) 患者的 GLI3 治疗靶点提供了依据。意义:我们描述了两种导致 GLI3 信号过度激活和增强 AR/GLI3 串扰的临床相关机制,这表明 GLI3 特异性抑制剂可能被证明有效,以阻止前列腺癌的发展或延迟 CRPC。