Abstract |
The PI-3 kinase pathway is a major driving force for human cancer. One common way of stimulating the PI-3 kinase pathway occurs through inactivation of the PTEN tumor suppressor. The mechanisms of PTEN inactivation include mutation, epigenetic silencing and post-translational modification. Improved insight into the regulation of PTEN is leading to a richer understanding of the contribution of PTEN and the PI-3 kinase pathway to human tumors. Understanding the pathology of PI-3 kinase signaling in tumors improves knowledge of cancer etiology and provides novel therapeutic targets.
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Authors | Ramon Parsons |
Journal | Seminars in cell & developmental biology
(Semin Cell Dev Biol)
Vol. 15
Issue 2
Pg. 171-6
(Apr 2004)
ISSN: 1084-9521 [Print] England |
PMID | 15209376
(Publication Type: Journal Article, Review)
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Chemical References |
- Tumor Suppressor Proteins
- Phosphatidylinositol 3-Kinases
- Phosphoric Monoester Hydrolases
- PTEN Phosphohydrolase
- PTEN protein, human
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Topics |
- Animals
- Chromosomes, Human, Pair 10
(genetics)
- Humans
- Neoplasms
(enzymology, metabolism, pathology, therapy)
- PTEN Phosphohydrolase
- Phosphatidylinositol 3-Kinases
(metabolism)
- Phosphoric Monoester Hydrolases
(chemistry, metabolism)
- Signal Transduction
- Tumor Suppressor Proteins
(chemistry, metabolism)
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