A secreted PTEN phosphatase that enters cells to alter signaling and survival. Academic Article uri icon

Overview

abstract

  • Phosphatase and tensin homolog on chromosome ten (PTEN) is a tumor suppressor and an antagonist of the phosphoinositide-3 kinase (PI3K) pathway. We identified a 576-amino acid translational variant of PTEN, termed PTEN-Long, that arises from an alternative translation start site 519 base pairs upstream of the ATG initiation sequence, adding 173 N-terminal amino acids to the normal PTEN open reading frame. PTEN-Long is a membrane-permeable lipid phosphatase that is secreted from cells and can enter other cells. As an exogenous agent, PTEN-Long antagonized PI3K signaling and induced tumor cell death in vitro and in vivo. By providing a means to restore a functional tumor-suppressor protein to tumor cells, PTEN-Long may have therapeutic uses.

authors

  • Hopkins, Benjamin David
  • Fine, Barry
  • Steinbach, Nicole
  • Dendy, Meaghan
  • Rapp, Zachary
  • Shaw, Jacquelyn
  • Pappas, Kyrie
  • Yu, Jennifer S
  • Hodakoski, Cindy
  • Mense, Sarah
  • Klein, Joshua
  • Pegno, Sarah
  • Sulis, Maria-Luisa
  • Goldstein, Hannah
  • Amendolara, Benjamin
  • Lei, Liang
  • Maurer, Matthew
  • Bruce, Jeffrey
  • Canoll, Peter
  • Hibshoosh, Hanina
  • Parsons, Ramon

publication date

  • June 6, 2013

Research

keywords

  • Cell Survival
  • PTEN Phosphohydrolase
  • Phosphatidylinositol 3-Kinase
  • Signal Transduction

Identity

PubMed Central ID

  • PMC3935617

Scopus Document Identifier

  • 84880737776

Digital Object Identifier (DOI)

  • 10.1126/science.1234907

PubMed ID

  • 23744781

Additional Document Info

volume

  • 341

issue

  • 6144