| Literature DB >> 22884032 |
L Braccini1, E Ciraolo, M Martini, T Pirali, G Germena, K Rolfo, E Hirsch.
Abstract
Epidemiological studies have established a positive correlation between cancer and metabolic disorders, suggesting that aberrant cell metabolism is a common feature of nearly all tumors. To meet their demand of building block molecules, cancer cells switch to a heavily glucose-dependent metabolism. As insulin triggers glucose uptake, most tumors are or become insulin-dependent. However, the effects of insulin and of other similar growth factors are not only limited to metabolic control but also favor tumor growth by stimulating proliferation and survival. A key signaling event mediating these metabolic and proliferative responses is the activation of the phosphatidylinositol-3 kinases (PI3K) pathway. In this review, we will thus discuss the current concepts of tumor metabolism and the opportunity of PI3K-targeted therapies to exploit the "sweet tooth" of cancer cells.Entities:
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Year: 2012 PMID: 22884032 DOI: 10.1016/j.jbior.2012.04.002
Source DB: PubMed Journal: Adv Biol Regul ISSN: 2212-4926