Targeting therapeutic liabilities engendered by PIK3R1 mutations for cancer treatment

Pharmacogenomics. 2016 Feb;17(3):297-307. doi: 10.2217/pgs.15.174. Epub 2016 Jan 25.

Abstract

The regulatory subunit of PI3K, p85α (encoded by PIK3R1), binds, stabilizes and inhibits the PI3K p110 catalytic subunit. Functional characterization of PIK3R1 mutations has identified not only hypomorphs with reduced inhibition of p110, but also hypomorphs and dominant negative mutants that disrupt a novel regulatory role of p85α on PTEN or neomorphs that activate unexpected signaling pathways. The diverse phenotypic spectrum of these PIK3R1 driver mutations underscores the need for different treatment strategies targeting tumors harboring these mutations. This article describes the functional consequences of the spectrum of PIK3R1 driver mutations and therapeutic liabilities they may engender.

Keywords: MAPK; PI3K; PIK3R1; mutation; p85; targeted therapy.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use*
  • Class Ia Phosphatidylinositol 3-Kinase
  • Humans
  • Mutation
  • Neoplasms / drug therapy*
  • Neoplasms / genetics
  • PTEN Phosphohydrolase / metabolism
  • Phosphatidylinositol 3-Kinases / genetics*
  • Phosphatidylinositol 3-Kinases / metabolism
  • Protein Binding
  • Protein Multimerization
  • Signal Transduction

Substances

  • Antineoplastic Agents
  • PIK3R1 protein, human
  • Class Ia Phosphatidylinositol 3-Kinase
  • PTEN Phosphohydrolase