Northern Institute for Cancer Research, Newcastle University, Paul O'Gorman Building, Framlington Place, Newcastle upon Tyne, Ne2 4HH, UK.
Sci Rep. 2017 Feb 16;7:40957. doi: 10.1038/srep40957.
Androgen receptor variants (AR-Vs) provide a mechanism of therapy evasion in castrate-resistant prostate cancer (CRPC), yet mechanisms of regulation remain largely unknown. Here we investigate the role of Aurora A kinase on AR-Vs in models of CRPC and show depletion of Aurora A reduces AR-V target gene expression. Importantly, knockdown of Aurora A reconfigures splicing of AR pre-mRNA to discriminately down-regulate synthesis of AR-V transcripts, including AR-V7, without effecting full-length AR mRNA; and as a consequence, AR-V-driven proliferation and survival of CRPC cells is markedly reduced. Critically, these effects are reproduced by Aurora A inhibition. We show that Aurora A levels increase in advanced disease and AURKA is an AR-V target gene demonstrating a positive feedback mechanism of androgenic signalling in CRPC. In all, our data suggests that Aurora A plays a pivotal role in regulation of AR-V7 expression and represents a new therapeutic target in CRPC.
雄激素受体变体(AR-Vs)为去势抵抗性前列腺癌(CRPC)的治疗逃逸提供了一种机制,但调节机制在很大程度上仍不清楚。在这里,我们研究了 Aurora A 激酶在 CRPC 模型中对 AR-Vs 的作用,并表明 Aurora A 的耗竭减少了 AR-V 靶基因的表达。重要的是,Aurora A 的敲低将 AR 前体 mRNA 的剪接重新配置为有区别地下调包括 AR-V7 在内的 AR-V 转录本的合成,而不影响全长 AR mRNA;因此,AR-V 驱动的 CRPC 细胞的增殖和存活明显减少。至关重要的是,这些作用可以通过 Aurora A 抑制来重现。我们表明,Aurora A 的水平在晚期疾病中增加,AURKA 是 AR-V 的靶基因,证明了 CRPC 中雄激素信号的正反馈机制。总之,我们的数据表明,Aurora A 在 AR-V7 表达的调节中发挥着关键作用,是 CRPC 的一个新的治疗靶点。