Correlation Engine 2.0
Clear Search sequence regions


  • Akt (13)
  • AMPK (1)
  • apoptosis (4)
  • c myc (15)
  • cell growth (1)
  • essential (1)
  • gene (1)
  • kinases (2)
  • mice (3)
  • mice knockout (1)
  • neu (9)
  • oncogenes (1)
  • protein kinases (2)
  • Pten (4)
  • pten protein (1)
  • regulates (1)
  • up regulates (1)
  • Sizes of these terms reflect their relevance to your search.

    The protooncogenes Akt and c-myc each positively regulate cell growth and proliferation, but have opposing effects on cell survival. These oncogenes cooperate to promote tumorigenesis, in part because the prosurvival effects of Akt offset the proapoptotic effects of c-myc. Akt's ability to counterbalance c-myc's proapoptotic effects has primarily been attributed to Akt-induced stimulation of prosurvival pathways that indirectly antagonize the effects of c-myc. We report a more direct mechanism by which Akt modulates the proapoptotic effects of c-myc. Specifically, we demonstrate that Akt up-regulates the adenosine monophosphate-associated kinase (AMPK)-related protein kinase, Hormonally up-regulated neu-associated kinase (Hunk), which serves as an effector of Akt prosurvival signaling by suppressing c-myc expression in a kinase-dependent manner to levels that are compatible with cell survival. Consequently, Akt pathway activation in the mammary glands of Hunk(-/-) mice results in induction of c-myc expression to levels that induce apoptosis. c-myc knockdown rescues the increase in apoptosis induced by Hunk deletion in cells in which Akt has been activated, indicating that repression of c-myc is a principal mechanism by which Hunk mediates the prosurvival effects of Akt. Consistent with this mechanism of action, we find that Hunk is required for c-myc suppression and mammary tumorigenesis induced by phosphatase and tensin homolog (Pten) deletion in mice. Together, our findings establish a prosurvival function for Hunk in tumorigenesis, define an essential mechanism by which Akt suppresses c-myc-induced apoptosis, and identify Hunk as a previously unrecognized link between the Akt and c-myc oncogenic pathways.

    Citation

    Elizabeth S Yeh, George K Belka, Ann E Vernon, Chien-Chung Chen, Jason J Jung, Lewis A Chodosh. Hunk negatively regulates c-myc to promote Akt-mediated cell survival and mammary tumorigenesis induced by loss of Pten. Proceedings of the National Academy of Sciences of the United States of America. 2013 Apr 09;110(15):6103-8

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 23520049

    View Full Text