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Regulation of FGF23: Beyond Bone.
Petra Simic1,2, Jodie L Babitt3,4
1Nephrology Division, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA. psimic@mgh.harvard.edu.
Fibroblast growth factor 23 (FGF23) regulates phosphate and vitamin D levels. New research reveals FGF23 interacts with iron, inflammation, and metabolism, impacting its own regulation and function.
Area of Science:
- Endocrinology
- Mineral Metabolism
- Bone Biology
Background:
- Fibroblast growth factor 23 (FGF23) is a key hormone derived from bone and bone marrow.
- It plays a critical role in maintaining phosphate homeostasis and regulating vitamin D synthesis.
- Dysregulation of FGF23 leads to conditions like hyperphosphatemia or hypophosphatemia, with significant health consequences.
Purpose of the Study:
- To review the current understanding of FGF23 regulation.
- To explore the intricate relationship between FGF23 and non-bone mineral factors.
- To highlight novel insights into FGF23's regulatory mechanisms and functional roles.
Main Methods:
- Review of existing scientific literature on FGF23.
- Analysis of studies investigating FGF23 interactions with various biological factors.
- Synthesis of findings on the bidirectional relationship between FGF23 and non-classical regulators.
Main Results:
- FGF23 levels are influenced by factors beyond bone mineral metabolism, including iron, erythropoietin, inflammation, energy, and metabolism.
- These factors impact both Fgf23 gene expression and FGF23 protein cleavage.
- FGF23 itself may play a role in regulating these non-bone mineral biological processes.
Conclusions:
- The regulation of FGF23 is complex and involves a bidirectional interplay with various systemic factors.
- Understanding these interactions provides new perspectives on FGF23's role in health and disease, particularly in kidney disease.
- Further research into these relationships could uncover new therapeutic targets for FGF23-related disorders.
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