Targeting therapeutic liabilities engendered by PIK3R1 mutations for cancer treatment

Lydia Wt Cheung, Gordon Mills

Research output: Contribution to journalReview article

11 Scopus citations

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.

Original languageEnglish (US)
Pages (from-to)297-307
Number of pages11
JournalPharmacogenomics
Volume17
Issue number3
DOIs
Publication statusPublished - Feb 1 2016
Externally publishedYes

    Fingerprint

Keywords

  • MAPK
  • mutation
  • p85
  • PI3K
  • PIK3R1
  • targeted therapy

ASJC Scopus subject areas

  • Molecular Medicine
  • Genetics
  • Pharmacology

Cite this