Cholesterol-rich lipid rafts mediate akt-regulated survival in prostate cancer cells

Cancer Res. 2002 Apr 15;62(8):2227-31.

Abstract

Although cholesterol accumulation in tumors was first reported in the early20th century, the mechanistic implications of this observation are still obscure. Here we report that caveolin-negative human prostate cancer (LNCaP) cells contain cholesterol-rich lipid rafts that mediate epidermal growth factor (EGF)-induced and constitutive signaling through the Akt1 serine-threonine kinase. EGF receptor and Akt1 phosphorylation were inhibited and autonomous cell survival was reduced when the rafts were disrupted. Reconstitution of the rafts with cholesterol restored EGF receptor-->Akt1 axis signaling and cytoprotection from a phosphoinositide 3-kinase-dependent apoptotic signal. These results suggest that cholesterol present in membrane microdomains is a prominent mediator of survival in prostate cancer cells.

Publication types

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

MeSH terms

  • Cell Membrane / metabolism
  • Cell Survival / physiology
  • Cholesterol / metabolism
  • Cholesterol / physiology*
  • Epidermal Growth Factor / pharmacology
  • ErbB Receptors / physiology
  • Humans
  • Male
  • Membrane Lipids / metabolism
  • Membrane Lipids / pharmacology
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphatidylinositol 3-Kinases / physiology
  • Prostatic Neoplasms / enzymology
  • Prostatic Neoplasms / metabolism*
  • Prostatic Neoplasms / pathology*
  • Protein Serine-Threonine Kinases*
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins / physiology*
  • Proto-Oncogene Proteins c-akt
  • Recombinant Proteins / pharmacology
  • Signal Transduction / physiology

Substances

  • Membrane Lipids
  • Proto-Oncogene Proteins
  • Recombinant Proteins
  • Epidermal Growth Factor
  • Cholesterol
  • ErbB Receptors
  • AKT1 protein, human
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-akt