The Phosphoinositide 3-Kinase/Akt1/Par-4 Axis: A Cancer-Selective Therapeutic Target
Open Access
- 15 March 2006
- journal article
- review article
- Published by American Association for Cancer Research (AACR) in Cancer Research
- Vol. 66 (6) , 2889-2892
- https://doi.org/10.1158/0008-5472.can-05-4458
Abstract
Activation of the phosphoinositide 3-kinase (PI3K)/Akt cell survival pathway in many cancers makes it an appealing target for therapeutic development. However, because this pathway also has an important role in the survival of normal cells, tactics to achieve cancer selectivity may prove important. We recently showed that the cancer-selective proapoptotic protein Par-4 is a key target for inactivation by PI3K/Akt signaling. Additionally, we found that Par-4 participates in mediating apoptosis by PTEN, the tumor suppressor responsible for blocking PI3K/Akt signaling. As a central player in cancer cell survival, Par-4 may provide a useful focus for the development of cancer-selective therapeutics. (Cancer Res 2006; 66(6): 2889-92)Keywords
This publication has 17 references indexed in Scilit:
- Binding and Phosphorylation of Par-4 by Akt Is Essential for Cancer Cell SurvivalMolecular Cell, 2005
- Phosphorylation of Par-4 by Protein Kinase A Is Critical for ApoptosisMolecular and Cellular Biology, 2005
- Identification of a Unique Core Domain of Par-4 Sufficient for Selective Apoptosis Induction in Cancer CellsMolecular and Cellular Biology, 2003
- The phosphatidylinositol 3-Kinase–AKT pathway in human cancerNature Reviews Cancer, 2002
- PTEN: Life as a Tumor SuppressorExperimental Cell Research, 2001
- The Hallmarks of CancerCell, 2000
- Negative regulation of Par-4 by oncogenic Ras is essential for cellular transformationOncogene, 1999
- Modulation of cellular apoptotic potential: contributions to oncogenesisOncogene, 1999
- Decreased expression of the pro-apoptotic protein Par-4 in renal cell carcinomaOncogene, 1999
- Mutually exclusive expression patterns of Bcl-2 and Par-4 in human prostate tumors consistent with down-regulation of Bcl-2 by Par-4Oncogene, 1999