Abstract
Both vascular endothelial growth factor A (VEGF) and osteopontin (OPN) can directly induce tumor angiogenesis, which is essential for the growth and metastasis of solid tumors. Here we engineered a bispecific antibody (VEGF/OPN-BsAb) using the anti-VEGF-A antibody bevacizumab and the anti-OPN antibody hu1A12. Compared with hu1A12 alone and bevacizumab alone, VEGF/OPN-BsAb was significantly more effective in inhibiting tumor angiogenesis in a highly metastatic human hepatocellular carcinoma nude mouse model. Further study demonstrated that VEGF/OPN-BsAb could effectively suppress primary tumor growth and metastasis to lungs, suggesting that it might be a promising therapeutic agent for treatment of metastatic cancer.
Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.
Publication types
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Research Support, N.I.H., Extramural
MeSH terms
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Animals
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Antibodies, Bispecific / immunology
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Antibodies, Bispecific / pharmacology*
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Antibodies, Monoclonal / immunology
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Antibodies, Monoclonal / pharmacology
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Antibodies, Monoclonal, Humanized
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Bevacizumab
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CHO Cells
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Cell Line, Tumor
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Cell Proliferation / drug effects
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Cells, Cultured
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Cricetinae
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Cricetulus
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Female
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Humans
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Kinetics
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Liver Neoplasms, Experimental / pathology
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Liver Neoplasms, Experimental / prevention & control
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Lung Neoplasms / prevention & control
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Lung Neoplasms / secondary
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Mice
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Mice, Inbred BALB C
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Mice, Nude
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Neoplasms / pathology
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Neoplasms / prevention & control*
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Neovascularization, Pathologic / prevention & control
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Osteopontin / antagonists & inhibitors*
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Osteopontin / genetics
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Osteopontin / immunology
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Protein Binding / immunology
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Reverse Transcriptase Polymerase Chain Reaction
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Tumor Burden / drug effects
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Vascular Endothelial Growth Factor A / antagonists & inhibitors*
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Vascular Endothelial Growth Factor A / genetics
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Vascular Endothelial Growth Factor A / immunology
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Xenograft Model Antitumor Assays
Substances
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Antibodies, Bispecific
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Antibodies, Monoclonal
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Antibodies, Monoclonal, Humanized
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Vascular Endothelial Growth Factor A
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Osteopontin
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Bevacizumab