Akt/PKB signaling pathway

The Akt signaling pathway or PI3K-Akt signaling pathway is a signal transduction pathway that promotes survival and growth in response to extracellular signals. Key proteins involved are PI3K (phosphatidylinositol 3-kinase) and Akt (protein kinase B).

Initial stimulation by one of the growth factors causes activation of a cell surface receptor and phosphorylation of PI3K. Activated PI3K then phosphorylates lipids on the plasma membrane, forming second messenger phosphatidylinositol (3,4,5)-trisphosphate (PIP3). Akt, a serine/threonine kinase, is recruited to the membrane by interaction with these phosphoinositide docking sites, so that it can be fully activated.[1] Activated Akt mediates downstream responses, including cell survival, growth, proliferation, cell migration and angiogenesis, by phosphorylating a range of intracellular proteins. The pathway is present in all cells of higher eukaryotes and is highly conserved.[2]

The pathway is highly regulated by multiple mechanisms, often involving cross-talk with other signaling pathways. Problems with PI3K-Akt pathway regulation can lead to an increase in signaling activity. This has been linked to a range of diseases such as cancer and type 2 diabetes. A major antagonist of PI3K activity is PTEN (phosphatase and tensin homolog), a tumour suppressor which is often mutated or lost in cancer cells. Akt phosphorylates as many as 100 different substrates, leading to a wide range of effects on cells.[3]

  1. ^ Osaki M, Oshimura M, Ito H (2004). "The PI3K-Akt pathway: Its functions and alterations in human cancer". Apoptosis. 9 (6): 667–676. doi:10.1023/B:APPT.0000045801.15585.dd. PMID 15505410. S2CID 13346655.
  2. ^ Manning BD, Cantley LC (2007). "AKT/PKB Signaling: Navigating Downstream". Cell. 129 (7): 1261–1274. doi:10.1016/j.cell.2007.06.009. PMC 2756685. PMID 17604717.
  3. ^ Cite error: The named reference Carracedo2008 was invoked but never defined (see the help page).

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