NEDD4 family E3 ligases in osteoporosis: mechanisms and emerging potential therapeutic targets

被引:0
|
作者
Wu, Heng [1 ]
Zuo, Junhui [1 ]
Dai, Yu [2 ]
Li, Hairui [3 ]
Wang, Song [1 ]
机构
[1] Southwest Med Univ, Affiliated Hosp, Dept Orthoped, Luzhou 646000, Peoples R China
[2] Southwest Med Univ, Affiliated Hosp, Dept Oncol, Luzhou 646000, Peoples R China
[3] Sichuan Univ, West China Hosp, Dept Urol, Chengdu 610041, Peoples R China
来源
关键词
Osteoporosis; Ubiquitination; E3 ubiquitin ligase; NEDD4 ubiquitin ligase family; Therapeutics; MESENCHYMAL STEM-CELLS; GROWTH-FACTOR-BETA; REGULATES CRANIOFACIAL DEVELOPMENT; UBIQUITIN LIGASES; HECT DOMAIN; OSTEOBLAST DIFFERENTIATION; BONE-MARROW; WW; DEGRADATION; HEALTH;
D O I
10.1186/s13018-025-05517-5
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Osteoporosis is a systemic skeletal disorder characterized by reduced bone density and an increased risk of fractures, particularly prevalent in the aging population. Osteoporotic complications, including vertebral compression fractures, hip fractures, and distal forearm fractures, affect over 8.9 million individuals globally, placing a significant economic strain on healthcare systems. Recent advances have expanded our understanding of the mechanisms underlying osteoporosis, particularly the intricate regulatory networks involved in bone metabolism. A central player in these processes is ubiquitin-mediated proteasomal degradation, a crucial post-translational modification system that involves ubiquitin, the ubiquitin-activating enzyme (E1), ubiquitin-conjugating enzyme (E2), ubiquitin ligase (E3), deubiquitinating enzymes, and the proteasome. Among the various E3 ligases, the NEDD4 family has emerged as a key regulator of both bone development and osteoporotic pathology. This review delineates the role of NEDD4 family in osteoporosis and identifies potential drug targets within these pathways, offering insights into novel therapeutic approaches for osteoporosis through targeted intervention.
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页数:12
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