| Literature DB >> 28455214 |
Chen Kan1, Lijun Chen1, Yangyang Hu1, Na Ding1, Haimei Lu1, Yuyun Li2, John A Kessler3, Lixin Kan4.
Abstract
Heterotopic ossification (HO), a serious disorder of extra-skeletal bone formation, occurs as a common complication of trauma or in rare genetic disorders. Many conserved signaling pathways have been implicated in HO; however, the exact underlying molecular mechanisms for many forms of HO are still unclear. The emerging picture is that dysregulation of bone morphogenetic protein (BMP) signaling plays a central role in the process, but that other conserved signaling pathways, such as Hedgehog (HH), Wnt/β-catenin and Fibroblast growth factors (FGF), are also involved, either through cross-talk with BMP signaling or through other independent mechanisms. Deep understanding of the conserved signaling pathways is necessary for the effective prevention and treatment of HO. In this review, we update and integrate recent progress in this area. Hopefully, our discussion will point to novel promising, druggable loci for further translational research and successful clinical applications.Entities:
Keywords: Bone morphogenetic protein (BMP); Conserved signaling pathways; Fibroblast growth factor (FGF); Fibrodysplasia ossificans progressiva (FOP); Hedgehog (HH); Heterotopic ossification (HO); Transforming growth factor β (TGF-β); Wnt/β-catenin
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Year: 2017 PMID: 28455214 PMCID: PMC5801212 DOI: 10.1016/j.bone.2017.04.014
Source DB: PubMed Journal: Bone ISSN: 1873-2763 Impact factor: 4.398