Epigenetics, Bone Remodeling and Osteoporosis

被引:9
|
作者
Yang, Shaoqing [1 ]
Duan, Xiaohong [1 ]
机构
[1] Fourth Mil Med Univ, Natl Clin Res Ctr Oral Dis, Shaanxi Key Lab Oral Dis,State Key Lab Mil Stom, Dept Oral Biol,Clin Oral Rare & Genet Dis,Sch Sto, 145 West Changle Rd, Xian 710032, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Epigenetic; DNA methylation; histone modification; bone remodeling; osteoblastogenesis; osteoclastogenesis; osteoporosis; HISTONE DEACETYLASE INHIBITORS; MESENCHYMAL STEM-CELLS; DE-NOVO METHYLATION; DNA METHYLATION; OSTEOGENIC DIFFERENTIATION; OSTEOCLAST DIFFERENTIATION; IN-VIVO; RECEPTOR ACTIVATOR; OSTEOCALCIN GENE; OSTEOBLAST;
D O I
10.2174/1574888X11666161221125656
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background: Osteoporosis is a common degenerative bone disease which is characterized with decreased bone strength and increased risk of fracture. The abnormal bone metabolism homeostasis, especially in osteoclastic function, takes a fundamental role in osteoporosis pathogenesis. In the past decade, epigenetic regulation of bone homeostasis are widely investigated and considered as a vital factor in the regulation of the differentiation and functions of osteoblasts, osteoclasts and osteocytes. The relationship between osteoporosis and epigenetic regulations has gradually become as an important issue in the mechanism study of osteoporosis. Objective: In this review, we summarize the recent progresses of epigenetic regulation mechanism in bone development and remodeling, and emphasize the epigenetic features of osteoporosis and the potent therapy application of epigenetic drugs for osteoporosis. Conclusion: DNA methylation and histone modification regulated bone development and remodeling via affecting both osteoblastogenesis and osteoclastogenesis. And the abnormal epigenetic status is relevant to bone disease such as osteoporosis and osteoarthritis. Several inhibitors of DNMTs or HDACs exhibit a potential application for osteoporosis, and the side effects of these drugs should also be considered in the future applications.
引用
收藏
页码:101 / 109
页数:9
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