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ERα in the Control of Mitochondrial Function and Metabolic Health

期刊

TRENDS IN MOLECULAR MEDICINE
卷 27, 期 1, 页码 31-46

出版社

CELL PRESS
DOI: 10.1016/j.molmed.2020.09.006

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资金

  1. National Institutes of Health [DK89109, DK063491, U54DK120342]
  2. NIH Nuclear Receptor Signaling Atlas (NURSA NDSP) [U24DK097748]
  3. UCLA Department of Medicine
  4. UCLA Iris-Cantor Women's Health Foundation
  5. UCLA Jonsson Comprehensive Cancer Center

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Decreases in metabolic health increase the risk of diseases such as type 2 diabetes, heart disease, and certain cancers. Reduced expression of ERα in muscle is associated with features of metabolic syndrome in women, men, and animals. Studies show a positive correlation between muscle expression of ERα and markers of metabolic health, including insulin sensitivity, highlighting the potential role of ERα-regulated pathways in disease prevention and improving women's health.
Decrements in metabolic health elevate disease risk, including type 2 diabetes, heart disease, and certain cancers. Thus, treatment strategies to combat metabolic dysfunction are needed. Reduced ESR1 (estrogen receptor, ER alpha) expression is observed in muscle from women, men, and animals presenting clinical features of the metabolic syndrome. Human studies of natural expression of ESR1 in metabolic tissues show that muscle expression of ESR1 is positively correlated with markers of metabolic health, including insulin sensitivity. Herein, we highlight the important impact of ER alpha on mitochondrial form and function and present how these actions of the receptor govern metabolic homeostasis. Studies identifying ER alpha-regulated pathways for disease prevention will lay the foundation for the design of novel therapeutics to improve the health of women while limiting secondary complications that have plagued traditional hormone replacement interventions.

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