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Bevacizumab (Avastin), a humanized anti-VEGF monoclonal antibody for cancer therapy.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2005 Jul 29; Vol. 333 (2), pp. 328-35. - Publication Year :
- 2005
-
Abstract
- Vascular endothelial growth factor (VEGF) is an endothelial cell-specific mitogen in vitro and an angiogenic inducer in vivo. The tyrosine kinases Flt-1 (VEGFR-1) and Flk-1/KDR (VEGFR-2) are high affinity VEGF receptors. VEGF plays an essential role in developmental angiogenesis and is important also for reproductive and bone angiogenesis. Substantial evidence also implicates VEGF as a mediator of pathological angiogenesis. Anti-VEGF monoclonal antibodies and other VEGF inhibitors block the growth of several tumor cell lines in nude mice. Clinical trials with VEGF inhibitors in a variety of malignancies are ongoing. Recently, a humanized anti-VEGF monoclonal antibody (bevacizumab; Avastin) has been approved by the FDA as a first-line treatment for metastatic colorectal cancer in combination with chemotherapy. Furthermore, VEGF is implicated in intraocular neovascularization associated with diabetic retinopathy and age-related macular degeneration.
- Subjects :
- Animals
Antibodies, Monoclonal, Humanized
Antineoplastic Agents administration & dosage
Bevacizumab
Clinical Trials as Topic
Humans
Neoplasms immunology
Neoplasms metabolism
Neovascularization, Pathologic immunology
Neovascularization, Pathologic metabolism
Treatment Outcome
Vascular Endothelial Growth Factor A immunology
Angiogenesis Inhibitors administration & dosage
Antibodies, Monoclonal administration & dosage
Neoplasms blood supply
Neoplasms drug therapy
Neovascularization, Pathologic prevention & control
Vascular Endothelial Growth Factor A metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0006-291X
- Volume :
- 333
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 15961063
- Full Text :
- https://doi.org/10.1016/j.bbrc.2005.05.132