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Endoglin: An accessory component of the TGF-beta-binding receptor-complex with diagnostic, prognostic, and bioimmunotherapeutic potential in human malignancies.
- Source :
-
Journal of cellular physiology [J Cell Physiol] 2001 Jul; Vol. 188 (1), pp. 1-7. - Publication Year :
- 2001
-
Abstract
- Endoglin (CD105) is a cell membrane glycoprotein over-expressed on highly proliferating endothelial cells in culture, and on endothelial cells of angiogenetic blood vessels within benign and malignant tissues. CD105 binds several factors of the Transforming Growth Factor (TGF)-beta superfamily, and its over-expression modulates cellular responses to TGF-beta1. The complex of experimental findings accumulated in the last few years strongly indicate that CD105 is a powerful marker of angiogenesis, and that it might play a critical role in the pathogenesis of vascular diseases and in tumor progression. In this paper, we will review the structural, biological and functional features of CD105, as well as its distribution within normal and neoplastic tissues, emphasizing its foreseeable role as a molecular target for new diagnostic and bioimmunotherapeutic approaches in human malignancies.<br /> (Copyright 2001 Wiley-Liss, Inc.)
- Subjects :
- Animals
Antigens, CD
Biomarkers, Tumor metabolism
Endoglin
Endothelium, Vascular cytology
Endothelium, Vascular metabolism
Humans
Macromolecular Substances
Neoplasms blood supply
Neoplasms pathology
Neoplasms therapy
Neovascularization, Physiologic physiology
Receptors, Cell Surface
Transforming Growth Factor beta genetics
Vascular Cell Adhesion Molecule-1 chemistry
Vascular Cell Adhesion Molecule-1 genetics
Neoplasms metabolism
Neovascularization, Pathologic physiopathology
Transforming Growth Factor beta metabolism
Vascular Cell Adhesion Molecule-1 metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0021-9541
- Volume :
- 188
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Journal of cellular physiology
- Publication Type :
- Academic Journal
- Accession number :
- 11382917
- Full Text :
- https://doi.org/10.1002/jcp.1095