Insulin-like growth factor-II regulates PTEN expression in the mammary gland

J Biol Chem. 2003 Dec 12;278(50):50422-7. doi: 10.1074/jbc.M306894200. Epub 2003 Sep 29.

Abstract

The tumor suppressor PTEN is altered in many cancers, including breast cancer, but only a handful of factors are known to control its expression. PTEN plays a vital role in cell survival and proliferation by regulating Akt phosphorylation, a key component of the phosphatidylinositol 3 kinase (PI3K) pathway. Here we show that insulin-like growth factor-II (IGF-II), which signals through PI3K, regulates PTEN expression in the mammary gland. IGF-II injection into mouse mammary gland significantly increased PTEN expression. Transgenic IGF-II expression also increased mammary PTEN protein, leading to reductions in Akt phosphorylation, epithelial proliferation, and mammary morphogenesis. IGF-II induced PTEN promoter activity and protein levels and this involved the immediate early gene egr-1. Thus, we have identified a novel negative feedback loop within the PI3K pathway where IGF-II induces PTEN expression to modulate its physiologic effects.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Blotting, Western
  • Cell Division
  • Cell Survival
  • DNA-Binding Proteins / metabolism
  • Dose-Response Relationship, Drug
  • Early Growth Response Protein 1
  • Epithelial Cells / metabolism
  • Feedback, Physiological
  • Gene Expression Regulation*
  • Immediate-Early Proteins*
  • Insulin-Like Growth Factor II / metabolism
  • Insulin-Like Growth Factor II / physiology*
  • Luciferases / metabolism
  • Mammary Glands, Animal / metabolism*
  • Mice
  • Mice, Transgenic
  • PTEN Phosphohydrolase
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphoric Monoester Hydrolases / biosynthesis*
  • Phosphoric Monoester Hydrolases / genetics
  • Phosphorylation
  • Promoter Regions, Genetic
  • Reverse Transcriptase Polymerase Chain Reaction
  • Time Factors
  • Transcription Factors / metabolism
  • Transfection
  • Transgenes
  • Tumor Suppressor Proteins / biosynthesis*
  • Tumor Suppressor Proteins / genetics

Substances

  • DNA-Binding Proteins
  • Early Growth Response Protein 1
  • Egr1 protein, mouse
  • Immediate-Early Proteins
  • Transcription Factors
  • Tumor Suppressor Proteins
  • Insulin-Like Growth Factor II
  • Luciferases
  • Phosphatidylinositol 3-Kinases
  • Phosphoric Monoester Hydrolases
  • PTEN Phosphohydrolase