Cells (Apr 2020)

Targeting GSK3 and Associated Signaling Pathways Involved in Cancer

  • Przemysław Duda,
  • Shaw M. Akula,
  • Stephen L. Abrams,
  • Linda S. Steelman,
  • Alberto M. Martelli,
  • Lucio Cocco,
  • Stefano Ratti,
  • Saverio Candido,
  • Massimo Libra,
  • Giuseppe Montalto,
  • Melchiorre Cervello,
  • Agnieszka Gizak,
  • Dariusz Rakus,
  • James A. McCubrey

DOI
https://doi.org/10.3390/cells9051110
Journal volume & issue
Vol. 9, no. 5
p. 1110

Abstract

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Glycogen synthase kinase 3 (GSK-3) is a serine/threonine (S/T) protein kinase. Although GSK-3 originally was identified to have functions in regulation of glycogen synthase, it was subsequently determined to have roles in multiple normal biochemical processes as well as various disease conditions. GSK-3 is sometimes referred to as a moonlighting protein due to the multiple substrates and processes which it controls. Frequently, when GSK-3 phosphorylates proteins, they are targeted for degradation. GSK-3 is often considered a component of the PI3K/PTEN/AKT/GSK-3/mTORC1 pathway as GSK-3 is frequently phosphorylated by AKT which regulates its inactivation. AKT is often active in human cancer and hence, GSK-3 is often inactivated. Moreover, GSK-3 also interacts with WNT/β-catenin signaling and β-catenin and other proteins in this pathway are targets of GSK-3. GSK-3 can modify NF-κB activity which is often expressed at high levels in cancer cells. Multiple pharmaceutical companies developed small molecule inhibitors to suppress GSK-3 activity. In addition, various natural products will modify GSK-3 activity. This review will focus on the effects of small molecule inhibitors and natural products on GSK-3 activity and provide examples where these compounds were effective in suppressing cancer growth.

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