Abstract
The biological actions of the insulin-like growth factors IGF-I and IGF- II are mediated by their activation of the IGF-IR, a transmembrane tyrosine kinase linked to the ras-raf-MAPK cascade. Functional IGF-IRs are required for the cell to progress through the cell cycle. Most importantly, cells lacking this receptor cannot be transformed by any of a number of dominant oncogenes, a finding that proves that the presence of the IGF-IR is important for the development of a malignant phenotype. Consistent with this role, the IGF-IR displays a potent antiapoptotic effect, both in vitro and in vivo. Because of its key role in the transformation process, the IGF-IR is actively studied as a potential therapeutic target in different types of neoplastic growth.
Original language | English |
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Pages (from-to) | 71-92 |
Number of pages | 22 |
Journal | Critical Reviews in Oncogenesis |
Volume | 8 |
Issue number | 1 |
DOIs | |
State | Published - 1997 |
Keywords
- Cell cycle
- Oncogene
- Signal transduction
- Transcription
- Tumor suppressors
- Tyrosine kinase
- WT1
- p53