配体诱导的蛋白酶体雌激素受体α降解:新的参与者?

Nuclear receptor signaling Pub Date : 2006-01-01 Epub Date: 2006-02-08 DOI:10.1621/nrs.04004
Mathilde Calligé, Hélène Richard-Foy
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引用次数: 41

摘要

从这个角度来看,我们考虑了配体诱导的雌激素受体α (er α)降解的新方面。在这个过程中,CSN5/Jab1和CSN复合体可能扮演什么角色?我们比较了激素(雌激素)或纯拮抗剂(氟维司汀)诱导的erα降解,并回顾了激酶抑制剂和crm1依赖的核输出对erα降解和转录激活的影响。本文提出了一个整合这些新因子的erα作用模型,并讨论了激素诱导的erα降解与转录激活之间的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ligand-induced estrogen receptor alpha degradation by the proteasome: new actors?

Ligand-induced estrogen receptor alpha degradation by the proteasome: new actors?

In this perspective we consider new aspects of ligand-induced estrogen receptor alpha (ERalpha) degradation. What are the possible roles of CSN5/Jab1 and the CSN complex in this process? We compare hormone (estrogen) or pure antagonist (fulvestrant) induced degradation of ERalpha and review the effects of kinase-inhibitors and CRM1-dependent nuclear export on ERalpha degradation and transcription activation. A model for ERalpha action integrating these new actors is proposed and the relation between hormone-induced ERalpha degradation and transcription-activation is discussed.

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