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An Anti-VEGF-B Antibody Reduces Abnormal Tumor Vasculature and Enhances the Effects of Chemotherapy
by
Gong, Sylvia J.
, Cartwright, Glenn A.
, Parslow, Adam C.
, Rigopoulos, Angela
, Johns, Terrance G.
, Scott, Fiona E.
, Eriksson, Ulf
, Scott, Andrew M.
, Lee, Fook-Thean
, Burvenich, Ingrid J. G.
, Janes, Peter W.
, Cao, Diana
in
Angiogenesis
/ Antigens
/ Bevacizumab
/ Biodistribution
/ Blood vessels
/ Breast cancer
/ Cable television broadcasting industry
/ Cancer
/ Cancer therapies
/ Chemotherapy
/ Colorectal cancer
/ Colorectal carcinoma
/ Disease
/ Fatty acids
/ Glioma
/ Growth factors
/ Kidney cancer
/ Kinases
/ Liver cancer
/ Medical prognosis
/ Melanoma
/ Metastasis
/ Monoclonal antibodies
/ Neovascularization
/ Ovaries
/ Prostate
/ Protein binding
/ Proteins
/ Spleen
/ Squamous cell carcinoma
/ Stroma
/ Tumor cells
/ Tumors
/ Type 2 diabetes
/ Vascular endothelial growth factor
2024
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An Anti-VEGF-B Antibody Reduces Abnormal Tumor Vasculature and Enhances the Effects of Chemotherapy
by
Gong, Sylvia J.
, Cartwright, Glenn A.
, Parslow, Adam C.
, Rigopoulos, Angela
, Johns, Terrance G.
, Scott, Fiona E.
, Eriksson, Ulf
, Scott, Andrew M.
, Lee, Fook-Thean
, Burvenich, Ingrid J. G.
, Janes, Peter W.
, Cao, Diana
in
Angiogenesis
/ Antigens
/ Bevacizumab
/ Biodistribution
/ Blood vessels
/ Breast cancer
/ Cable television broadcasting industry
/ Cancer
/ Cancer therapies
/ Chemotherapy
/ Colorectal cancer
/ Colorectal carcinoma
/ Disease
/ Fatty acids
/ Glioma
/ Growth factors
/ Kidney cancer
/ Kinases
/ Liver cancer
/ Medical prognosis
/ Melanoma
/ Metastasis
/ Monoclonal antibodies
/ Neovascularization
/ Ovaries
/ Prostate
/ Protein binding
/ Proteins
/ Spleen
/ Squamous cell carcinoma
/ Stroma
/ Tumor cells
/ Tumors
/ Type 2 diabetes
/ Vascular endothelial growth factor
2024
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Do you wish to request the book?
An Anti-VEGF-B Antibody Reduces Abnormal Tumor Vasculature and Enhances the Effects of Chemotherapy
by
Gong, Sylvia J.
, Cartwright, Glenn A.
, Parslow, Adam C.
, Rigopoulos, Angela
, Johns, Terrance G.
, Scott, Fiona E.
, Eriksson, Ulf
, Scott, Andrew M.
, Lee, Fook-Thean
, Burvenich, Ingrid J. G.
, Janes, Peter W.
, Cao, Diana
in
Angiogenesis
/ Antigens
/ Bevacizumab
/ Biodistribution
/ Blood vessels
/ Breast cancer
/ Cable television broadcasting industry
/ Cancer
/ Cancer therapies
/ Chemotherapy
/ Colorectal cancer
/ Colorectal carcinoma
/ Disease
/ Fatty acids
/ Glioma
/ Growth factors
/ Kidney cancer
/ Kinases
/ Liver cancer
/ Medical prognosis
/ Melanoma
/ Metastasis
/ Monoclonal antibodies
/ Neovascularization
/ Ovaries
/ Prostate
/ Protein binding
/ Proteins
/ Spleen
/ Squamous cell carcinoma
/ Stroma
/ Tumor cells
/ Tumors
/ Type 2 diabetes
/ Vascular endothelial growth factor
2024
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An Anti-VEGF-B Antibody Reduces Abnormal Tumor Vasculature and Enhances the Effects of Chemotherapy
Journal Article
An Anti-VEGF-B Antibody Reduces Abnormal Tumor Vasculature and Enhances the Effects of Chemotherapy
2024
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Overview
The vascular endothelial growth factors (VEGFs) and their receptors (VEGFRs) are key regulators of blood vessel formation, including in tumors, where their deregulated function can promote the production of aberrant, leaky blood vessels, supporting tumor development. Here we investigated the VEGFR1 ligand VEGF-B, which we demonstrate to be expressed in tumor cells and in tumor stroma and vasculature across a range of tumor types. We examined the anti-VEGF-B-specific monoclonal antibody 2H10 in preclinical xenograft models of breast and colorectal cancer, in comparison with the anti-VEGF-A antibody bevacizumab. Similar to bevacizumab, 2H10 therapy was associated with changes in tumor blood vessels and intra-tumoral diffusion consistent with normalization of the tumor vasculature. Accordingly, treatment resulted in partial inhibition of tumor growth, and significantly improved the response to chemotherapy. Our studies indicate the importance of VEGF-B in tumor growth, and the potential of specific anti-VEGF-B treatment to inhibit tumor development, alone or in combination with established chemotherapies.
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