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[Osteoporosis and RANKL signal].

Abstract
Osteoporosis is caused by imbalance between osteoclastic bone resorption and osteoblastic bone formation. From the recent results of several kinds of knockout mice, osteoclast differentiation factor (RANKL) and its soluble decoy receptor for RANKL (OPG) are essentially involved in pathogenesis of osteoporosis. Deficiency of RANKL in human has been shown to result in osteopetrosis. Furthermore, it has been reported that anti-RANKL neutralizing antibody (denosumab) will be effective new drug for osteoporosis.
AuthorsMidori Nakamura, Nobuyuki Udagawa
JournalClinical calcium (Clin Calcium) Vol. 21 Issue 8 Pg. 1149-55 (Aug 2011) ISSN: 0917-5857 [Print] Japan
PMID21814019 (Publication Type: English Abstract, Journal Article, Review)
Chemical References
  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • Osteoprotegerin
  • RANK Ligand
  • Denosumab
Topics
  • Animals
  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • Bone Resorption (genetics)
  • Cell Differentiation (genetics)
  • Denosumab
  • Drug Design
  • Humans
  • Mice
  • Molecular Targeted Therapy
  • Mutation
  • Osteoblasts
  • Osteoclasts (cytology)
  • Osteopetrosis (genetics)
  • Osteoporosis (drug therapy, genetics)
  • Osteoprotegerin (physiology)
  • RANK Ligand (genetics, immunology, physiology)
  • Signal Transduction (physiology)

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