4.7 Review

The multiple universes of estrogen-related receptor α and γ in metabolic control and related diseases

Journal

ACTA PHARMACOLOGICA SINICA
Volume 36, Issue 1, Pages 51-61

Publisher

ACTA PHARMACOLOGICA SINICA
DOI: 10.1038/aps.2014.121

Keywords

diabetes; energy metabolism; fatty liver; glucose; metabolic syndrome; mitochondria; nuclear receptors; oxidative phosphorylation; skeletal muscle

Funding

  1. Canadian Institutes of Health Research (CIHR)
  2. Fonds de recherche du Quebec-Sante (FRQS)
  3. McGill Integrated Cancer Research Training Program (MICRTP)
  4. CIHR [MOP-111144, 125885]
  5. Terry Fox Research Institute [TFF-116128]

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The identification of the estrogen-related receptors (ERRs) as the first orphan nuclear receptors ignited a new era in molecular endocrinology, which led to the discovery of new ligand-dependent response systems. Although ERR subfamily members have yet to be associated with a natural ligand, the characterization of these orphan receptors has demonstrated that they occupy a strategic node in the transcriptional control of cellular energy metabolism. In particular, ERRs are required for the response to various environmental challenges that require high energy levels by the organism. As central regulators of energy homeostasis, ERRs may also be implicated in the etiology of metabolic disorders, such as type 2 diabetes and metabolic syndrome. Here, we review the recent evidence that further highlights the role of ERRs in metabolic control, particularly in liver and skeletal muscle, and their likely involvement in metabolic diseases. Consequently, we also explore the promises and pitfalls of ERRs as potential therapeutic targets.

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