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首页> 外文期刊>Oncogene >DHX15 promotes prostate cancer progression by stimulating Siah2-mediated ubiquitination of androgen receptor
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DHX15 promotes prostate cancer progression by stimulating Siah2-mediated ubiquitination of androgen receptor

机译:DHX15通过刺激Siah2介导的雄激素受体泛素化促进前列腺癌的进展

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摘要

Androgen receptor (AR) activation is critical for prostate cancer (PCa) development and progression, including castration resistance. The nuclear export signal of AR (NES~(AR)) has an important role in AR intracellular trafficking and proteasome-dependent degradation. Here, we identified the RNA helicase DHX15 as a novel AR co-activator using a yeast mutagenesis screen and revealed that DHX15 regulates AR activity by modulating E3 ligase Siah2-mediated AR ubiquitination independent of its ATPase activity. DHX15 and Siah2 form a complex with AR, through NES~(AR). DHX15 stabilized Siah2 and enhanced its E3 ubiquitin-ligase activity, resulting in AR activation. Importantly, DHX15 was upregulated in PCa specimens and its expression was correlated with Gleason scores and prostate-specific antigen recurrence. Furthermore, DHX15 immunostaining correlated with Siah2. Finally, DHX15 knockdown inhibited the growth of C4-2 prostate tumor xenografts in mice. Collectively, our data argue that DHX15 enhances AR transcriptional activity and contributes to PCa progression through Siah2.
机译:雄激素受体(AR)的激活对于前列腺癌(PCa)的发展和进展(包括去势抵抗)至关重要。 AR的核输出信号(NES_(AR))在AR细胞内运输和蛋白酶体依赖性降解中具有重要作用。在这里,我们使用酵母诱变筛选将RNA解旋酶DHX15鉴定为新型AR共激活因子,并揭示DHX15通过调节E3连接酶Siah2介导的AR泛素化而独立于其ATPase活性来调节AR活性。 DHX15和Siah2通过NES〜(AR)与AR形成复合体。 DHX15稳定Siah2并增强其E3泛素连接酶活性,从而导致AR活化。重要的是,DHX15在PCa标本中上调,其表达与格里森评分和前列腺特异性抗原复发相关。此外,DHX15免疫染色与Siah2相关。最后,DHX15组合式抑制小鼠C4-2前列腺肿瘤异种移植的生长。总体而言,我们的数据认为DHX15增强了AR转录活性,并通过Siah2促进了PCa进程。

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