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极光激酶 A 在去势抵抗性前列腺癌模型中调节 AR-V7 的表达。

Aurora A regulates expression of AR-V7 in models of castrate resistant prostate cancer.

机构信息

Northern Institute for Cancer Research, Newcastle University, Paul O'Gorman Building, Framlington Place, Newcastle upon Tyne, Ne2 4HH, UK.

出版信息

Sci Rep. 2017 Feb 16;7:40957. doi: 10.1038/srep40957.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b913/5311967/5f165d1bc193/srep40957-f1.jpg

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