Savoy Rosalinda M, Chen Liqun, Siddiqui Salma, Melgoza Frank U, Durbin-Johnson Blythe, Drake Christiana, Jathal Maitreyee K, Bose Swagata, Steele Thomas M, Mooso Benjamin A, D'Abronzo Leandro S, Fry William H, Carraway Kermit L, Mudryj Maria, Ghosh Paramita M
VA Northern California Health Care SystemMather, California, USADepartment of UrologySchool of Medicine, University of California Davis, 4860 Y Street, Suite 3500, Sacramento, California 95817, USADivision of BiostatisticsDepartment of Public Health Sciences, University of California Davis, Davis, California, USADepartment of StatisticsUniversity of California Davis, Davis, California, USADepartment of Biochemistry and Molecular MedicineUniversity of California Davis, Sacramento, California, USADepartment of Medical Microbiology and ImmunologyUniversity of California Davis, Davis, California, USA VA Northern California Health Care SystemMather, California, USADepartment of UrologySchool of Medicine, University of California Davis, 4860 Y Street, Suite 3500, Sacramento, California 95817, USADivision of BiostatisticsDepartment of Public Health Sciences, University of California Davis, Davis, California, USADepartment of StatisticsUniversity of California Davis, Davis, California, USADepartment of Biochemistry and Molecular MedicineUniversity of California Davis, Sacramento, California, USADepartment of Medical Microbiology and ImmunologyUniversity of California Davis, Davis, California, USA.
VA Northern California Health Care SystemMather, California, USADepartment of UrologySchool of Medicine, University of California Davis, 4860 Y Street, Suite 3500, Sacramento, California 95817, USADivision of BiostatisticsDepartment of Public Health Sciences, University of California Davis, Davis, California, USADepartment of StatisticsUniversity of California Davis, Davis, California, USADepartment of Biochemistry and Molecular MedicineUniversity of California Davis, Sacramento, California, USADepartment of Medical Microbiology and ImmunologyUniversity of California Davis, Davis, California, USA.
Endocr Relat Cancer. 2015 Jun;22(3):369-86. doi: 10.1530/ERC-15-0021. Epub 2015 Mar 10.
Prostate cancer (PCa) progression is regulated by the androgen receptor (AR); however, patients undergoing androgen-deprivation therapy (ADT) for disseminated PCa eventually develop castration-resistant PCa (CRPC). Results of previous studies indicated that AR, a transcription factor, occupies distinct genomic loci in CRPC compared with hormone-naïve PCa; however, the cause of this distinction was unknown. The E3 ubiquitin ligase Nrdp1 is a model AR target modulated by androgens in hormone-naïve PCa but not in CRPC. Using Nrdp1, we investigated how AR switches transcription programs during CRPC progression. The proximal Nrdp1 promoter contains an androgen response element (ARE); we demonstrated AR binding to this ARE in androgen-sensitive PCa. Analysis of hormone-naive human prostatectomy specimens revealed correlation between Nrdp1 and AR expression, supporting AR regulation of NRDP1 levels in androgen-sensitive tissue. However, despite sustained AR levels, AR binding to the Nrdp1 promoter and Nrdp1 expression were suppressed in CRPC. Elucidation of the suppression mechanism demonstrated correlation of NRDP1 levels with nuclear localization of the scaffolding protein filamin A (FLNA) which, as we previously showed, is itself repressed following ADT in many CRPC tumors. Restoration of nuclear FLNA in CRPC stimulated AR binding to Nrdp1 ARE, increased its transcription, and augmented NRDP1 protein expression and responsiveness to ADT, indicating that nuclear FLNA controls AR-mediated androgen-sensitive Nrdp1 transcription. Expression of other AR-regulated genes lost in CRPC was also re-established by nuclear FLNA. Thus, our results indicate that nuclear FLNA promotes androgen-dependent AR-regulated transcription in PCa, while loss of nuclear FLNA in CRPC alters the AR-regulated transcription program.
前列腺癌(PCa)的进展受雄激素受体(AR)调控;然而,接受雄激素剥夺疗法(ADT)治疗播散性PCa的患者最终会发展为去势抵抗性PCa(CRPC)。先前研究结果表明,作为一种转录因子,AR在CRPC中占据的基因组位点与激素初治PCa不同;然而,这种差异的原因尚不清楚。E3泛素连接酶Nrdp1是激素初治PCa中受雄激素调控的AR靶标模型,但在CRPC中并非如此。我们利用Nrdp1研究了AR在CRPC进展过程中如何切换转录程序。Nrdp1近端启动子含有一个雄激素反应元件(ARE);我们证实在雄激素敏感的PCa中AR与该ARE结合。对激素初治的人类前列腺切除标本分析显示Nrdp1与AR表达之间存在相关性,支持AR对雄激素敏感组织中NRDP1水平的调控。然而,尽管AR水平持续存在,但在CRPC中AR与Nrdp1启动子的结合以及Nrdp1的表达均受到抑制。对抑制机制的阐明表明NRDP1水平与支架蛋白细丝蛋白A(FLNA)的核定位相关,正如我们之前所表明的,在许多CRPC肿瘤中,ADT后FLNA本身会受到抑制。在CRPC中恢复核FLNA可刺激AR与Nrdp1 ARE结合,增加其转录,并增强NRDP1蛋白表达及对ADT的反应性,表明核FLNA控制AR介导的雄激素敏感的Nrdp1转录。CRPC中丢失的其他AR调控基因的表达也通过核FLNA得以重新建立。因此,我们的结果表明核FLNA促进PCa中雄激素依赖的AR调控转录,而CRPC中核FLNA的缺失改变了AR调控的转录程序。