Extracellular Signal-Regulated Kinase 7, a Regulator of Hormone-Dependent Estrogen Receptor Destruction

Author:

Henrich Lorin M.12,Smith Jeffrey A.32,Kitt Danielle12,Errington Timothy M.12,Nguyen Binh12,Traish Abdulmaged M.4,Lannigan Deborah A.12

Affiliation:

1. Department of Microbiology

2. Center for Cell Signaling, University of Virginia, Charlottesville, Virginia 22908

3. Department of Pathology

4. Department of Biochemistry, Boston University School of Medicine, Boston, Massachusetts 02118

Abstract

ABSTRACT Estrogen receptor alpha (ERα) degradation is regulated by ubiquitination, but the signaling pathways that modulate ERα turnover are unknown. We found that extracellular signal-regulated kinase 7 (ERK7) preferentially enhances the destruction of ERα but not the related androgen receptor. Loss of ERK7 was correlated with breast cancer progression, and all ERα-positive breast tumors had decreased ERK7 expression compared to that found in normal breast tissue. In human breast cells, a dominant-negative ERK7 mutant decreased the rate of endogenous ERα degradation >4-fold in the presence of hormone and potentiated estrogen responsiveness. ERK7 targets the ERα ligand-binding domain for destruction by enhancing its ubiquitination. Thus, ERK7 is a novel regulator of estrogen responsiveness through its control of ERα turnover.

Publisher

American Society for Microbiology

Subject

Cell Biology,Molecular Biology

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