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The role of CKIP-1 in osteoporosis development and treatment
Osteoporosis is a systemic skeletal disorder characterized by reduced bone mass and deterioration of bone microarchitecture, which results in increased bone fragility and fracture risk. Casein kinase 2-interacting protein-1 (CKIP-1) is a protein that plays an important role in regulation of bone for...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5895943/ https://www.ncbi.nlm.nih.gov/pubmed/29682283 http://dx.doi.org/10.1302/2046-3758.72.BJR-2017-0172.R1 |
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author | Peng, X. Wu, X. Zhang, J. Zhang, G. Li, G. Pan, X. |
author_facet | Peng, X. Wu, X. Zhang, J. Zhang, G. Li, G. Pan, X. |
author_sort | Peng, X. |
collection | PubMed |
description | Osteoporosis is a systemic skeletal disorder characterized by reduced bone mass and deterioration of bone microarchitecture, which results in increased bone fragility and fracture risk. Casein kinase 2-interacting protein-1 (CKIP-1) is a protein that plays an important role in regulation of bone formation. The effect of CKIP-1 on bone formation is mainly mediated through negative regulation of the bone morphogenetic protein pathway. In addition, CKIP-1 has an important role in the progression of osteoporosis. This review provides a summary of the recent studies on the role of CKIP-1 in osteoporosis development and treatment. Cite this article: X. Peng, X. Wu, J. Zhang, G. Zhang, G. Li, X. Pan. The role of CKIP-1 in osteoporosis development and treatment. Bone Joint Res 2018;7:173–178. DOI: 10.1302/2046-3758.72.BJR-2017-0172.R1. |
format | Online Article Text |
id | pubmed-5895943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-58959432018-04-20 The role of CKIP-1 in osteoporosis development and treatment Peng, X. Wu, X. Zhang, J. Zhang, G. Li, G. Pan, X. Bone Joint Res Systematic Review: Research Osteoporosis is a systemic skeletal disorder characterized by reduced bone mass and deterioration of bone microarchitecture, which results in increased bone fragility and fracture risk. Casein kinase 2-interacting protein-1 (CKIP-1) is a protein that plays an important role in regulation of bone formation. The effect of CKIP-1 on bone formation is mainly mediated through negative regulation of the bone morphogenetic protein pathway. In addition, CKIP-1 has an important role in the progression of osteoporosis. This review provides a summary of the recent studies on the role of CKIP-1 in osteoporosis development and treatment. Cite this article: X. Peng, X. Wu, J. Zhang, G. Zhang, G. Li, X. Pan. The role of CKIP-1 in osteoporosis development and treatment. Bone Joint Res 2018;7:173–178. DOI: 10.1302/2046-3758.72.BJR-2017-0172.R1. 2018-04-12 /pmc/articles/PMC5895943/ /pubmed/29682283 http://dx.doi.org/10.1302/2046-3758.72.BJR-2017-0172.R1 Text en © 2018 Peng et al. This is an open-access article distributed under the terms of the Creative Commons Attributions licence (CC-BY-NC), which permits unrestricted use, distribution, and reproduction in any medium, but not for commercial gain, provided the original author and source are credited. |
spellingShingle | Systematic Review: Research Peng, X. Wu, X. Zhang, J. Zhang, G. Li, G. Pan, X. The role of CKIP-1 in osteoporosis development and treatment |
title | The role of CKIP-1 in osteoporosis development and treatment |
title_full | The role of CKIP-1 in osteoporosis development and treatment |
title_fullStr | The role of CKIP-1 in osteoporosis development and treatment |
title_full_unstemmed | The role of CKIP-1 in osteoporosis development and treatment |
title_short | The role of CKIP-1 in osteoporosis development and treatment |
title_sort | role of ckip-1 in osteoporosis development and treatment |
topic | Systematic Review: Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5895943/ https://www.ncbi.nlm.nih.gov/pubmed/29682283 http://dx.doi.org/10.1302/2046-3758.72.BJR-2017-0172.R1 |
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