Literature DB >> 27163679

Targeting VEGF and Its Receptors for the Treatment of Osteoarthritis and Associated Pain.

John L Hamilton1, Masashi Nagao2, Brett R Levine3, Di Chen1, Bjorn R Olsen2, Hee-Jeong Im1,3,4,5,6.   

Abstract

Increased vascular endothelial growth factor (VEGF) levels are associated with osteoarthritis (OA) progression. Indeed, VEGF appears to be involved in OA-specific pathologies including cartilage degeneration, osteophyte formation, subchondral bone cysts and sclerosis, synovitis, and pain. Moreover, a wide range of studies suggest that inhibition of VEGF signaling reduces OA progression. This review highlights both the potential significance of VEGF in OA pathology and pain, as well as potential benefits of inhibition of VEGF and its receptors as an OA treatment. With the emergence of the clinical use of anti-VEGF therapy outside of OA, both as high-dose systemic treatments and low-dose local treatments, these particular therapies are now more widely understood. Currently, there is no established disease-modifying drug available for patients with OA, which warrants continued study of the inhibition of VEGF signaling in OA, as stand-alone or adjuvant therapy.
© 2016 American Society for Bone and Mineral Research. © 2016 American Society for Bone and Mineral Research.

Entities:  

Keywords:  ANGIOGENESIS; OSTEOARTHRITIS; VASCULAR ENDOTHELIAL GROWTH FACTOR (VEGF); VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR (VEGFR)

Mesh:

Substances:

Year:  2016        PMID: 27163679      PMCID: PMC4863467          DOI: 10.1002/jbmr.2828

Source DB:  PubMed          Journal:  J Bone Miner Res        ISSN: 0884-0431            Impact factor:   6.741


  199 in total

1.  Thrombospondin-1 inhibits VEGF receptor-2 signaling by disrupting its association with CD47.

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Journal:  J Biol Chem       Date:  2010-10-05       Impact factor: 5.157

2.  Analysis of biological effects and signaling properties of Flt-1 (VEGFR-1) and KDR (VEGFR-2). A reassessment using novel receptor-specific vascular endothelial growth factor mutants.

Authors:  H Gille; J Kowalski; B Li; J LeCouter; B Moffat; T F Zioncheck; N Pelletier; N Ferrara
Journal:  J Biol Chem       Date:  2000-10-31       Impact factor: 5.157

Review 3.  The basic science of the subchondral bone.

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Review 4.  Importance of subchondral bone to articular cartilage in health and disease.

Authors:  H Imhof; M Breitenseher; F Kainberger; T Rand; S Trattnig
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6.  Molecular cloning of a new class of cartilage-specific matrix, chondromodulin-I, which stimulates growth of cultured chondrocytes.

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Journal:  Biochem Biophys Res Commun       Date:  1991-03-29       Impact factor: 3.575

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10.  Changes in the antiangiogenic properties of articular cartilage in osteoarthritis.

Authors:  James O Smith; Richard O C Oreffo; Nicholas M P Clarke; Helmtrud I Roach
Journal:  J Orthop Sci       Date:  2003       Impact factor: 1.601

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  70 in total

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2.  Altered protein levels in bone marrow lesions of hip osteoarthritis: Analysis by proteomics and multiplex immunoassays.

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4.  Transcriptome-Wide Analyses of Human Neonatal Articular Cartilage and Human Mesenchymal Stem Cell-Derived Cartilage Provide a New Molecular Target for Evaluating Engineered Cartilage.

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5.  Targeting vascular endothelial growth factor ameliorates PMMA-particles induced inflammatory osteolysis in murine calvaria.

Authors:  Wahid Abu-Amer; Manoj Arra; John C F Clohisy; Yousef Abu-Amer; Gaurav Swarnkar
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6.  Platelet-Rich Plasma Released From Polyethylene Glycol Hydrogels Exerts Beneficial Effects on Human Chondrocytes.

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Review 7.  Hypertension meets osteoarthritis - revisiting the vascular aetiology hypothesis.

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Review 10.  Vascular Endothelial Growth Factor Biology and Its Potential as a Therapeutic Target in Rheumatic Diseases.

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