成为目标的 pERK:孤儿核受体ERRγ的激酶调控。

Receptors & clinical investigation Pub Date : 2014-01-01
Rebecca B Riggins
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引用次数: 0

摘要

雌激素相关受体(ERRs)是核受体超家族中的孤儿成员,是线粒体代谢的重要调节因子,在癌症中发挥着新的作用。在没有内源性配体的情况下,ERRs 依赖于其他调控机制,包括蛋白质/蛋白质相互作用和翻译后修饰,但后者的细胞和临床意义尚不清楚。我们最近发表了一项研究,将雌激素相关受体γ(ERRγ)确定为细胞外信号调节激酶(ERK)的靶点,并表明ERK对ERRγ的调节对雌激素受体阳性(ER+)乳腺癌细胞模型中该受体的功能具有重要影响。在本研究亮点中,我们将从分子和临床角度讨论这些发现的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The pERK of being a target: Kinase regulation of the orphan nuclear receptor ERRγ.

The pERK of being a target: Kinase regulation of the orphan nuclear receptor ERRγ.

Estrogen-related receptors (ERRs) are orphan members of the nuclear receptor superfamily that are important regulators of mitochondrial metabolism with emerging roles in cancer. In the absence of an endogenous ligand, ERRs are reliant upon other regulatory mechanisms that include protein/protein interactions and post-translational modification, though the cellular and clinical significance of this latter mechanism is unclear. We recently published a study in which we establish estrogen-related receptor gamma (ERRγ) as a target for extracellular signal-regulated kinase (ERK), and show that regulation of ERRγ by ERK has important consequences for the function of this receptor in cellular models of estrogen receptor-positive (ER+) breast cancer. In this Research Highlight, we discuss the implications of these findings from a molecular and clinical perspective.

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