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TGF-β: duality of function between tumor prevention and carcinogenesis.
- Source :
-
Journal of the National Cancer Institute [J Natl Cancer Inst] 2014 Feb; Vol. 106 (2), pp. djt369. - Publication Year :
- 2014
-
Abstract
- Several mechanisms underlying tumor progression have remained elusive, particularly in relation to transforming growth factor beta (TGF-β). Although TGF-β initially inhibits epithelial growth, it appears to promote the progression of advanced tumors. Defects in normal TGF-β pathways partially explain this paradox, which can lead to a cascade of downstream events that drive multiple oncogenic pathways, manifesting as several key features of tumorigenesis (uncontrolled proliferation, loss of apoptosis, epithelial-to-mesenchymal transition, sustained angiogenesis, evasion of immune surveillance, and metastasis). Understanding the mechanisms of TGF-β dysregulation will likely reveal novel points of convergence between TGF-β and other pathways that can be specifically targeted for therapy.
- Subjects :
- Animals
Cadherins metabolism
Carcinogenesis metabolism
Disease Progression
Humans
Neoplasms chemically induced
Neoplasms prevention & control
Neovascularization, Pathologic chemically induced
Neovascularization, Pathologic prevention & control
Protein Serine-Threonine Kinases metabolism
Receptor, Transforming Growth Factor-beta Type I
Receptors, Transforming Growth Factor beta metabolism
Up-Regulation
Anticarcinogenic Agents metabolism
Anticarcinogenic Agents pharmacology
Apoptosis
Carcinogens metabolism
Carcinogens pharmacology
Cell Proliferation
Cell Transformation, Neoplastic chemically induced
Cell Transformation, Neoplastic metabolism
Neoplasms metabolism
Signal Transduction
Transforming Growth Factor beta metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1460-2105
- Volume :
- 106
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Journal of the National Cancer Institute
- Publication Type :
- Academic Journal
- Accession number :
- 24511106
- Full Text :
- https://doi.org/10.1093/jnci/djt369