Exploring the impact of estrogen-related receptor gamma on metabolism and disease

•ERRγ is a key regulator of metabolic gene expression.•ERRγ is involved in crosstalk with the endocrine pathway and other metabolic pathways.•Dysregulation of ERRγ contributes to various diseases and metabolic conditions.•Targeting ERRγ is a potential approach for treating metabolic diseases. Estrog...

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Veröffentlicht in:Steroids 2024-11, Vol.211, p.109500, Article 109500
Hauptverfasser: Sadasivam, Nanthini, Park, Woo-Ram, Choi, Byungyoon, Seok Jung, Yoon, Choi, Hueng-Sik, Kim, Don-Kyu
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Sprache:eng
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Zusammenfassung:•ERRγ is a key regulator of metabolic gene expression.•ERRγ is involved in crosstalk with the endocrine pathway and other metabolic pathways.•Dysregulation of ERRγ contributes to various diseases and metabolic conditions.•Targeting ERRγ is a potential approach for treating metabolic diseases. Estrogen-related receptor gamma (ERRγ) is a member of the ERR orphan nuclear receptor family which possesses three subtypes, α, β, and γ. ERRγ is reportedly predominantly expressed in metabolically active tissues and cells, which promotes positive and negative effects in different tissues. ERRγ overexpression in the liver, pancreas, and thyroid cells is related to liver cancer, oxidative stress, reactive oxygen species (ROS) regulation, and carcinoma. Reduced ERRγ expression in the brain, immune cells, tumor cells, and energy metabolism causes neurological dysfunction, gastric cancer, and obesity. ERRγ is a constitutive receptor; however, its transcriptional activity also depends on co-regulators, agonists, and antagonists, which, when after forming a complex, can play a role in targeting and treating diseases. Moreover, ERRγ has proven crucial in regulating cellular and metabolic activity. However, many functions mediated via ERRγ remain unknown and require further exploration. Hence, considering the importance of ERRγ, this review focuses on the critical findings and interactions between ERRγ and co-regulators, agonists, and antagonists alongside its relationship with downstream and upstream signaling pathways and diseases. This review highlights new findings and provides a path to understanding the current ideas and future studies on ERRγ-mediated cellular activity.
ISSN:0039-128X
1878-5867
1878-5867
DOI:10.1016/j.steroids.2024.109500