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AKT 上调前列腺癌细胞中 B-Raf Ser445 的磷酸化和 ERK1/2 的激活,以应对雄激素耗竭。

AKT upregulates B-Raf Ser445 phosphorylation and ERK1/2 activation in prostate cancer cells in response to androgen depletion.

机构信息

Department of Biochemistry, Medical College of Wisconsin, 8701 Watertown Plank Road, Milwaukee, WI 53226, USA.

Department of Dermatology, Medical College of Wisconsin, Milwaukee, WI 53226, USA.

出版信息

Exp Cell Res. 2013 Jul 15;319(12):1732-1743. doi: 10.1016/j.yexcr.2013.05.008. Epub 2013 May 20.

Abstract

Upregulated ERK1/2 activity is often correlated with AKT activation during prostate cancer (PCa) progression, yet their functional relation needs elucidation. Using androgen-deprived LNCaP cells, in which ERK1/2 activation occurs in strong correlation with AKT activation, we found that AKT-mediated B-Raf regulation is necessary for ERK1/2 activation. Specifically, in response to androgen deprivation, AKT upregulated B-Raf phosphorylation at Ser445 without affecting A-Raf or C-Raf-1. This effect of AKT was abolished by Arg25 to Ala mutation or truncating (∆4-129) the pleckstrin homology domain of AKT, indicating that the canonical AKT regulation is important for this signaling. Intriguingly, although a constitutively active AKT containing N-terminal myristoylation signal could sufficiently upregulate B-Raf phosphorylation at Ser445 in LNCaP cells, subsequent MEK/ERK activation still required hormone deprivation. In contrast, AKT activity was sufficient to induce not only B-Raf phosphorylation but also MEK/ERK activation in the hormone refractory LNCaP variant, C4-2. These data indicate that androgen depletion may induce MEK/ERK activation through a synergy between AKT-dependent and -independent mechanisms and that the latter may become deregulated in association with castration resistance. In support, consistent AKT-mediated B-Raf regulation was also detected in a panel of PCa lines derived from the cPten(-/-)L mice before and after castration. Our results also demonstrate that AKT regulates androgen receptor levels partly via the Raf/MEK/ERK pathway. This study reveals a novel crosstalk between ERK1/2 and AKT in PCa cells.

摘要

ERK1/2 活性的上调通常与前列腺癌(PCa)进展过程中的 AKT 激活相关,但它们的功能关系仍需阐明。在雄激素剥夺的 LNCaP 细胞中,ERK1/2 的激活与 AKT 的激活强烈相关,我们发现 AKT 介导的 B-Raf 调节对于 ERK1/2 的激活是必要的。具体而言,在雄激素剥夺的情况下,AKT 上调了 B-Raf 在 Ser445 位的磷酸化,而不影响 A-Raf 或 C-Raf-1。AKT 的这种作用被 Arg25 突变为 Ala 或截断(∆4-129)AKT 的 pleckstrin 同源结构域所消除,表明经典的 AKT 调节对于这种信号转导很重要。有趣的是,虽然含有 N 端豆蔻酰化信号的组成型激活 AKT 足以在 LNCaP 细胞中充分上调 B-Raf 在 Ser445 位的磷酸化,但随后的 MEK/ERK 激活仍需要激素剥夺。相比之下,AKT 活性足以不仅诱导 B-Raf 磷酸化,而且在激素抵抗的 LNCaP 变体 C4-2 中诱导 MEK/ERK 激活。这些数据表明,雄激素耗竭可能通过 AKT 依赖性和非依赖性机制之间的协同作用诱导 MEK/ERK 激活,并且后者可能与去势抵抗相关而失调。支持这一观点的是,在 cPten(-/-)L 小鼠来源的一组 PCa 细胞系中,在去势前后也检测到一致的 AKT 介导的 B-Raf 调节。我们的研究结果还表明,AKT 部分通过 Raf/MEK/ERK 途径调节雄激素受体水平。这项研究揭示了 PCa 细胞中 ERK1/2 和 AKT 之间的一种新的串扰。

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