Antiangiogenic Peptides and Proteins: from Experimental Tools to Clinical Drugs.
From: Centre Pluridisciplinaire d’Oncologie, Faculty of Biology and Medicine, University of Lausanne, Epalinges s/Lausanne, Switzerland. curzio.ruegg@isrec.ch
Biochimica et biophysica acta
- Publish Date: Apr 2006
- ISSN: 0006-3002
- Volume: 1765
- Issue: 2
- Pages: 155-77
- Medium: Print
- Language: English
- Citation (JAMA): Rüegg Curzio, Hasmim Meriem, Lejeune Ferdy J, et al. Antiangiogenic Peptides and Proteins: from Experimental Tools to Clinical Drugs.. Biochim. Biophys. Acta Apr 2006;1765:155-77
Abstract
The formation of a ‘tumor-associated vasculature’, a process referred to as tumor angiogenesis, is a stromal reaction essential for tumor progression. Inhibition of tumor angiogenesis suppresses tumor growth in many experimental models, thereby indicating that tumor-associated vasculature may be a relevant target to inhibit tumor progression. Among the antiangiogenic molecules reported to date many are peptides and proteins. They include cytokines, chemokines, antibodies to vascular growth factors and growth factor receptors, soluble receptors, fragments derived from extracellular matrix proteins and small synthetic peptides. The polypeptide tumor necrosis factor (TNF, Beromun) was the first drug registered for the regional treatment of human cancer, whose mechanisms of action involved selective disruption of the tumor vasculature. More recently, bevacizumab (Avastin), an antibody against vascular endothelial growth factor (VEGF)-A, was approved as the first systemic antiangiogenic drug that had a significant impact on the survival of patients with advanced colorectal cancer, in combination with chemotherapy. Several additional peptides and antibodies with antiangiogenic activity are currently tested in clinical trials for their therapeutic efficacy. Thus, peptides, polypeptides and antibodies are emerging as leading molecules among the plethora of compounds with antiangiogenic activity. In this article, we will review some of these molecules and discuss their mechanism of action and their potential therapeutic use as anticancer agents in humans.
Mesh Headings (Keywords): Angiogenesis Inhibitors, Animals, Humans, Neoplasms, Neovascularization, Pathologic
Check for Full Text / PubMed Unique Identifier (PMID): 16263219
This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.
Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.
The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.
