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Deprecated: Implicit conversion from float 243.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Clin+Cancer+Res 2014 ; 20 (12): 3057-63 Nephropedia Template TP
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Molecular Pathways: PI 3-Kinase Pathway Phosphatases as Biomarkers for Cancer Prognosis and Therapy #MMPMID24928944
Chen M; Nowak DG; Trotman LC
Clin Cancer Res 2014[Jun]; 20 (12): 3057-63 PMID24928944show ga
Cancer research has seen tremendous changes over the past decade. Fast progress in sequencing technology has afforded us with landmark genetic alterations, which had immediate impact on clinical science and practice by pointing to new kinase targets, such as PI 3-Kinase, the EGF receptor or BRAF. The PI 3-Kinase pathway for growth control has emerged as a prime example for both oncogene activation and tumor suppressor loss in cancer.Here, we discuss how therapy using PI 3-kinase pathway inhibitors could benefit from information on specific phosphatases, which naturally antagonize the kinase targets. This PI 3-Kinase pathway is found mutated in most cancer types, including prostate, breast, colon and brain tumors. The tumor suppressing phosphatases operate at two levels. Lipid level phosphatases, such as PTEN and INPP4b revert PI 3-kinase activity to keep the lipid second messengers inactive. At the protein level, PHLPP1/2 protein phosphatases inactivate AKT kinase, thus antagonizing mTOR complex 2 activity. However, in contrast to their kinase counterparts the phosphatases are unlikely drug targets. They would need to be stimulated by therapy and are commonly deleted and mutated in cancer. Yet, since they occupy critical nodes in preventing cancer initiation and progression, the information on their status has tremendous potential in outcome prediction, and in matching the available kinase inhibitor repertoire with the right patients.