αvβ3 Integrin antagonists as inhibitors of bone resorption
- 1 June 2000
- journal article
- review article
- Published by Informa Healthcare in Expert Opinion on Investigational Drugs
- Vol. 9 (6) , 1281-1291
- https://doi.org/10.1517/13543784.9.6.1281
Abstract
The alpha(v)beta(3) integrin is a non-covalent, heterodimeric, cell-surface protein that is expressed with varying density on numerous cell types, including osteoclasts, vascular smooth muscle cells, endothelial cells and a variety of tumour cells. Functionally, alpha(v)beta(3) mediates a diverse range of biological events including the adhesion of osteoclasts to bone matrix, smooth muscle cell migration and angiogenesis. Specifically, there has been significant attention focused on the preparation of inhibitors of alpha(v)beta(3) for use as inhibitors of bone resorption, in recognition of the medical need for improved prevention and treatment of osteoporosis. Herein, we summarise the pertinent chemistry and biological advances in the medicinal design and biological evaluation of peptide and small molecule alpha(v)beta(3) antagonists as inhibitors of bone resorption.Keywords
This publication has 25 references indexed in Scilit:
- Cell adhesion: old and new questionsTrends in Cell Biology, 1999
- Requirement of Integrin β3 Tyrosine 747 for β3 Tyrosine Phosphorylation and Regulation of αvβ3 AvidityPublished by Elsevier ,1997
- The αvβ3 integrin “vitronectin receptor”The International Journal of Biochemistry & Cell Biology, 1997
- Agonist-activated αvμ3 on Platelets and Lymphocytes Binds to the Matrix Protein OsteopontinJournal of Biological Chemistry, 1997
- The Amino-terminal One-third of αIIb Defines the Ligand Recognition Specificity of Integrin αIIbβ3Published by Elsevier ,1996
- Regulation of Integrin Affinity States through an NP XY Motif in the β Subunit Cytoplasmic DomainJournal of Biological Chemistry, 1995
- Recognition of distinct adhesive sites on fibrinogen by related integrins on platelets and endothelial cellsCell, 1989
- Integrins: A family of cell surface receptorsCell, 1987
- cDNA and amino acid sequences of the cell adhesion protein receptor recognizing vitronectin reveal a transmembrane domain and homologies with other adhesion protein receptors.Proceedings of the National Academy of Sciences, 1986
- A 125/115-kDa cell surface receptor specific for vitronectin interacts with the arginine-glycine-aspartic acid adhesion sequence derived from fibronectin.Proceedings of the National Academy of Sciences, 1985