A kinase-independent function of AKT promotes cancer cell survival Journal Article


Authors: Vivanco, I.; Chen, Z. C.; Tanos, B.; Oldrini, B.; Hsieh, W. Y.; Yannuzzi, N.; Campos, C.; Mellinghoff, I. K.
Article Title: A kinase-independent function of AKT promotes cancer cell survival
Abstract: The serine-threonine kinase AKT regulates proliferation and survival by phosphorylating a network of protein substrates. Here we describe a kinase-independent function of AKT. In cancer cells harboring gain-of-function alterations in MET, HER2, or Phosphatidyl-Inositol-3-Kinase (PI3-K), catalytically-inactive AKT (K179M) protected from drug-induced cell death in a PH-domain dependent manner. An AKT kinase domain mutant found in human melanoma (G161V) lacked enzymatic activity in-vitro and in AKT1/AKT2 double knockout cells, but promoted growth-factor independent survival of primary human melanocytes. ATP-competitive AKT inhibitors failed to block the kinase-independent function of AKT, a liability that limits their effectiveness compared to allosteric AKT inhibitors. Our results broaden the current view of AKT function and have important implications for the development of AKT inhibitors for cancer.
Keywords: mutation; inhibitor; mechanism; activation; b/akt; 3-kinase; pleckstrin homology domain
Journal Title: eLife
Volume: 3
ISSN: 2050-084X
Publisher: eLife Sciences Publications Ltd.  
Date Published: 2014-12-31
Start Page: e03751
Language: English
ACCESSION: WOS:000347419300001
DOI: 10.7554/eLife.03751
PROVIDER: wos
PMCID: PMC4337624
PUBMED: 25551293
Notes: 13 page article -- Article -- Source: Wos
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  1. Igor Vivanco
    12 Vivanco
  2. Carl Campos
    37 Campos
  3. Zhi Cheng Michael Chen
    1 Chen