Inositol Polyphosphate-Based Compounds as Inhibitors of Phosphoinositide 3-Kinase-Dependent Signaling

Int J Mol Sci. 2020 Sep 29;21(19):7198. doi: 10.3390/ijms21197198.

Abstract

Signaling pathways regulated by the phosphoinositide 3-kinase (PI3K) enzymes have a well-established role in cancer development and progression. Over the past 30 years, the therapeutic potential of targeting this pathway has been well recognized, and this has led to the development of a multitude of drugs, some of which have progressed into clinical trials, with few of them currently approved for use in specific cancer settings. While many inhibitors compete with ATP, hence preventing the catalytic activity of the kinases directly, a deep understanding of the mechanisms of PI3K-dependent activation of its downstream effectors led to the development of additional strategies to prevent the initiation of this signaling pathway. This review summarizes previously published studies that led to the identification of inositol polyphosphates as promising parent molecules to design novel inhibitors of PI3K-dependent signals. We focus our attention on the inhibition of protein-membrane interactions mediated by binding of pleckstrin homology domains and phosphoinositides that we proposed 20 years ago as a novel therapeutic strategy.

Keywords: inositol 1,3,4,5,6-pentakisphosphate; inositol polyphosphates; phosphoinositide 3-kinase; phosphoinositides; pleckstrin homology domain.

Publication types

  • Review

MeSH terms

  • Humans
  • Inositol / chemistry
  • Inositol / therapeutic use
  • Phosphatidylinositol 3-Kinase / drug effects
  • Phosphatidylinositol 3-Kinase / genetics*
  • Phosphatidylinositols / therapeutic use*
  • Phosphoinositide-3 Kinase Inhibitors / therapeutic use*
  • Pleckstrin Homology Domains / drug effects
  • Signal Transduction / drug effects*

Substances

  • Phosphatidylinositols
  • Phosphoinositide-3 Kinase Inhibitors
  • Inositol
  • Phosphatidylinositol 3-Kinase