去势治疗诱导的上皮间质转化（Epithelial-mesenchymal transition, EMT）改变是前列腺癌CRPC发生及疾病进展重要原因。研究证实，β-catenin/snail2信号激活在其中发挥关键调节作用。但去势治疗激活β-catenin/snail2信号的具体机制尚不清楚。我们既往研究发现，PHF8受去势诱导的缺氧调控，敲低PHF8显著抑制去势诱导的snail2的转录活化及EMT改变。结合以往及我们的前期研究，我们推测：PHF8作为去势诱导的β-catenin/snail2信号激活的“开关”调节分子，在前列腺癌上皮间质转化中发挥重要作用。本项目拟以前列腺癌细胞、裸鼠移植瘤及PHF8基因敲除前列腺癌小鼠模型为研究对象，研究PHF8对β-catenin/snail2信号通路的调节机制及其在去势诱导的前列腺癌EMT中的作用。研究结果将揭示前列腺癌EMT新的调控机制，提高前列腺癌治疗效果，具有重要科学意义及潜在的临床应用价值。

Multiple lines of evidence suggest that castration treatment-induced Epithelial-mesenchymal transition (EMT) of prostate cancer plays crucial roles in the pathogenesis of castration resistant prostate cancer (CPRC) and disease progression. Previous studies demonstrated that the activation of β-catenin mediated snail2 signaling might be the main event during EMT process after long time of androgen deprivation therapy (ADT). However, the underlying molecular mechanism by which castration treatment activates β-catenin/snail2 signaling still remains unclear. Our previous findings showed that PHF8 is upregulated by HIFs （hypoxia inducible factors）in the condition of hypoxia induced by ADT. PHF8 knockdown could repress castration-induced transcription of snail2 and EMT process. Taken all together, we hypothesized that PHF8, as a ‘switch molecule’, might play an important regulatory role in the EMT process induced by ADT via activating β-catenin/snail2 signaling. In this study, by using prostate cancer cell lines, xenografts and a new mice model of prostatic carcinoma with PHF8 knockout background (TRAMP/PHF8-/Y) by crossing TRAMP (Transgenic Adenocarcinoma of the Mouse Prostate) with PHF8 knockout mice, we will investigate how PHF8 regulates the expressions of snail2, as well as their effects on ADT-induced EMT process. These studies will shed a new insight into understanding the molecular mechanisms underlying the development of CRPC as well as looking for the potential molecular target for therapeutic intervention of CRPC, which is of very important scientific significance as well as clinical value.