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The role of the fibroblast growth factor family in bone-related diseases
Jicheng Wang1,2, Shizhang Liu1, Jingyuan Li1
1Department of Orthopaedics, Shaanxi Provincial People's Hospital, Xi'an, China.
Abstract:
Fibroblast growth factor (FGF) family members are important regulators of cell growth, proliferation, differentiation, and regeneration. The abnormal expression of certain FGF family members can cause skeletal diseases, including achondroplasia, craniosynostosis syndrome, osteoarthritis, and Kashin-Beck disease. Accumulating evidence shows that FGFs play a crucial role in the growth and proliferation of bone and in the pathogenesis of certain bone-related diseases. Here, we review the involvement of FGFs in bone-related processes and diseases; FGF1 in the differentiation of human bone marrow mesenchymal stem cells and fracture repair; FGF2, FGF9, and FGF18 in osteoarthritis; FGF6 in bone and muscle injury; FGF8 in osteoarthritis and Kashin-Beck disease; and FGF21 and FGF23 on bone regulation. These findings indicate that FGFs are targets for novel therapeutic interventions for bone-related diseases.
Insights
Fibroblast growth factors (FGFs) regulate cell growth and are crucial in bone development and diseases. Targeting FGFs offers potential new therapies for skeletal conditions like osteoarthritis.
Area of Science:
- Molecular Biology
- Cell Biology
- Skeletal Biology
Background:
- Fibroblast growth factors (FGFs) are key regulators of cellular processes including growth, proliferation, differentiation, and regeneration.
- Aberrant expression of specific FGF family members is implicated in various skeletal disorders such as achondroplasia, craniosynostosis, osteoarthritis, and Kashin-Beck disease.
- FGFs play a significant role in bone growth, proliferation, and the pathogenesis of bone-related diseases.
Purpose of the Study:
- To review the multifaceted roles of FGFs in bone-related biological processes.
- To examine the involvement of specific FGF members in the pathogenesis of bone diseases.
- To highlight FGFs as potential therapeutic targets for skeletal disorders.
Main Methods:
- Literature review of studies investigating FGF family members and their functions in bone.
- Analysis of evidence linking specific FGFs (FGF1, FGF2, FGF6, FGF8, FGF9, FGF18, FGF21, FGF23) to bone-related processes and diseases.
- Synthesis of findings on FGFs' impact on cell differentiation, fracture repair, osteoarthritis, bone and muscle injury, and bone regulation.
Main Results:
- FGF1 is involved in human bone marrow mesenchymal stem cell differentiation and fracture repair.
- FGF2, FGF9, and FGF18 are associated with osteoarthritis.
- FGF6 plays a role in bone and muscle injury.
- FGF8 is implicated in osteoarthritis and Kashin-Beck disease.
- FGF21 and FGF23 are involved in bone regulation.
Conclusions:
- FGFs are critical mediators of bone development, regeneration, and disease.
- Specific FGF members have distinct roles in various skeletal pathologies.
- The FGF family represents a promising avenue for developing novel therapeutic strategies for bone-related diseases.
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