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EGFR Signaling: Friend or Foe for Cartilage?

Recent studies using genetically modified mice, pharmacological approaches, and human samples have highlighted an important role for the epidermal growth factor receptor (EGFR), selected ligands, and downstream components in endochondral bone formation and joint homeostasis. Although most data demon...

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Detalles Bibliográficos
Autores principales: Qin, Ling, Beier, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6383702/
https://www.ncbi.nlm.nih.gov/pubmed/30828691
http://dx.doi.org/10.1002/jbm4.10177
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author Qin, Ling
Beier, Frank
author_facet Qin, Ling
Beier, Frank
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description Recent studies using genetically modified mice, pharmacological approaches, and human samples have highlighted an important role for the epidermal growth factor receptor (EGFR), selected ligands, and downstream components in endochondral bone formation and joint homeostasis. Although most data demonstrate an important function of this pathway in endochondral ossification and articular cartilage growth, conflicting results on its role in osteoarthritis have been reported. In some contexts, inactivation of EGFR signaling has been shown to protect joints from surgically induced osteoarthritis, whereas in others, similar manipulations worsened joint pathology. The current review summarizes recent studies of cartilage EGFR signaling in long bone development and diseases, provides potential explanations for the reported discrepancies, and suggests directions for future work to clarify the potential of this pathway as target for osteoarthritis treatment. © 2019 The Authors. JBMR Plus published by Wiley Periodicals, Inc. on behalf of American Society for Bone and Mineral Research.
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spelling pubmed-63837022019-03-01 EGFR Signaling: Friend or Foe for Cartilage? Qin, Ling Beier, Frank JBMR Plus Review Recent studies using genetically modified mice, pharmacological approaches, and human samples have highlighted an important role for the epidermal growth factor receptor (EGFR), selected ligands, and downstream components in endochondral bone formation and joint homeostasis. Although most data demonstrate an important function of this pathway in endochondral ossification and articular cartilage growth, conflicting results on its role in osteoarthritis have been reported. In some contexts, inactivation of EGFR signaling has been shown to protect joints from surgically induced osteoarthritis, whereas in others, similar manipulations worsened joint pathology. The current review summarizes recent studies of cartilage EGFR signaling in long bone development and diseases, provides potential explanations for the reported discrepancies, and suggests directions for future work to clarify the potential of this pathway as target for osteoarthritis treatment. © 2019 The Authors. JBMR Plus published by Wiley Periodicals, Inc. on behalf of American Society for Bone and Mineral Research. John Wiley and Sons Inc. 2019-02-13 /pmc/articles/PMC6383702/ /pubmed/30828691 http://dx.doi.org/10.1002/jbm4.10177 Text en © 2019 The Authors. JBMR Plus published by Wiley Periodicals, Inc. on behalf of American Society for Bone and Mineral Research This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Qin, Ling
Beier, Frank
EGFR Signaling: Friend or Foe for Cartilage?
title EGFR Signaling: Friend or Foe for Cartilage?
title_full EGFR Signaling: Friend or Foe for Cartilage?
title_fullStr EGFR Signaling: Friend or Foe for Cartilage?
title_full_unstemmed EGFR Signaling: Friend or Foe for Cartilage?
title_short EGFR Signaling: Friend or Foe for Cartilage?
title_sort egfr signaling: friend or foe for cartilage?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6383702/
https://www.ncbi.nlm.nih.gov/pubmed/30828691
http://dx.doi.org/10.1002/jbm4.10177
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