Literature DB >> 16782455

Molecular bases of the regulation of bone remodeling by the canonical Wnt signaling pathway.

Donald A Glass1, Gerard Karsenty.   

Abstract

Osteoporosis is a common, prevalent, and debilitating condition, particularly in postmenopausal women. Genetics play a major role in determining peak bone mass and fracture risk, but few genes have been demonstrated conclusively to be involved, much less the signaling pathways with which they are affiliated. The identification of mutations in the gene Lrp5, a Wnt coreceptor, as the cause for both osteoporotic and high-bone mass disorders implicated the canonical Wnt signaling pathway in bone mass regulation. Since Lrp5, other Wnt components have been identified as being regulators of bone mass, and Wnt target genes affecting bone homeostasis have begun to be elucidated. This chapter looks at the various components of the canonical Wnt signaling pathway and the data indicating that this pathway plays a major role in the control of both bone formation and bone resorption, the two key aspects of bone remodeling.

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Year:  2006        PMID: 16782455     DOI: 10.1016/S0070-2153(05)73002-7

Source DB:  PubMed          Journal:  Curr Top Dev Biol        ISSN: 0070-2153            Impact factor:   4.897


  43 in total

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Review 7.  WNT signaling in bone development and homeostasis.

Authors:  Zhendong Zhong; Nicole J Ethen; Bart O Williams
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2014-09-30       Impact factor: 5.814

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Review 9.  From estrogen-centric to aging and oxidative stress: a revised perspective of the pathogenesis of osteoporosis.

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Journal:  Am J Stem Cells       Date:  2013-03-08
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