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Reversibility of epithelial-mesenchymal transition (EMT) induced in breast cancer cells by activation of urokinase receptor-dependent cell signaling

J Biol Chem. 2009 Aug 21;284(34):22825-33. doi: 10.1074/jbc.M109.023960. Epub 2009 Jun 22.

Abstract

Hypoxia induces expression of the urokinase receptor (uPAR) and activates uPAR-dependent cell signaling in cancer cells. This process promotes epithelial-mesenchymal transition (EMT). uPAR overexpression in cancer cells also promotes EMT. In this study, we tested whether uPAR may be targeted to reverse cancer cell EMT. When MDA-MB 468 breast cancer cells were cultured in 1% O(2), uPAR expression increased, as anticipated. Cell-cell junctions were disrupted, vimentin expression increased, and E-cadherin was lost from cell surfaces, indicating EMT. Transferring these cells back to 21% O(2) decreased uPAR expression and reversed the signs of EMT. In uPAR-overexpressing MDA-MB 468 cells, EMT was reversed by silencing expression of endogenously produced urokinase-type plasminogen activator (uPA), which is necessary for uPAR-dependent cell signaling, or by targeting uPAR-activated cell signaling factors, including phosphatidylinositol 3-kinase, Src family kinases, and extracellular signal-regulated kinase. MDA-MB 231 breast cancer cells express high levels of uPA and uPAR and demonstrate mesenchymal cell morphology under normoxic culture conditions (21% O(2)). Silencing uPA expression in MDA-MB-231 cells decreased expression of vimentin and Snail, and induced changes in morphology characteristic of epithelial cells. These results demonstrate that uPAR-initiated cell signaling may be targeted to reverse EMT in cancer.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Calcium-Calmodulin-Dependent Protein Kinases / antagonists & inhibitors
  • Cell Hypoxia / physiology
  • Cell Line, Tumor
  • Cell Movement
  • Chick Embryo
  • Chickens
  • Chromones / pharmacology
  • Epithelium / drug effects
  • Epithelium / metabolism
  • Epithelium / pathology*
  • Flavonoids / pharmacology
  • Humans
  • Immunoblotting
  • Mesoderm / drug effects
  • Mesoderm / metabolism
  • Mesoderm / pathology*
  • Microscopy, Fluorescence
  • Morpholines / pharmacology
  • Oxygen / pharmacology
  • Phosphoinositide-3 Kinase Inhibitors
  • Polymerase Chain Reaction
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / physiology
  • Receptors, Urokinase Plasminogen Activator / genetics
  • Receptors, Urokinase Plasminogen Activator / physiology*
  • Signal Transduction* / drug effects
  • Signal Transduction* / genetics
  • Tubulin / genetics
  • Urokinase-Type Plasminogen Activator / genetics
  • Urokinase-Type Plasminogen Activator / physiology
  • Vimentin / genetics

Substances

  • Chromones
  • Flavonoids
  • Morpholines
  • Phosphoinositide-3 Kinase Inhibitors
  • RNA, Small Interfering
  • Receptors, Urokinase Plasminogen Activator
  • Tubulin
  • Vimentin
  • 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Urokinase-Type Plasminogen Activator
  • Oxygen
  • 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one