The Na+/H+ exchanger NHE1, but not the Na+, HCO3(-) cotransporter NBCn1, regulates motility of MCF7 breast cancer cells expressing constitutively active ErbB2

Cancer Lett. 2012 Apr 28;317(2):172-83. doi: 10.1016/j.canlet.2011.11.023. Epub 2011 Nov 25.

Abstract

We and others have shown central roles of the Na(+)/H(+) exchanger NHE1 in cell motility. The aim of this study was to determine the roles of NHE1 and of the Na(+), HCO(3)(-) cotransporter NBCn1 in motility of serum-starved MCF-7 breast cancer cells expressing constitutively active ErbB2 (ΔNErbB2). ΔNErbB2 expression elicited NBCn1 upregulation, Ser(703)-phosphorylation of NHE1, and NHE1-inhibitor (EIPA)-sensitive pericellular acidification, in conjunction with increased expression of β1 integrin and ERM proteins. Active ERM proteins and NHE1 colocalized strongly to invadopodial rosettes, the diameter of which was increased by ΔNErbB2. Adhesion and migration on collagen-I were augmented by ΔNErbB2, unaffected by the NBC inhibitor S0859, and further stimulated by EIPA in a manner potentiated by PI3K-Akt-inhibition. These findings demonstrate that NHE1 inhibition can enhance cancer cell motility, adding an important facet to the understanding of NHE1 in cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amiloride / analogs & derivatives
  • Amiloride / pharmacology
  • Benzamides / pharmacology
  • Breast Neoplasms / genetics
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology
  • Cation Transport Proteins / genetics
  • Cation Transport Proteins / metabolism*
  • Cell Adhesion / drug effects
  • Cell Adhesion / genetics
  • Cell Adhesion / physiology
  • Cell Line, Tumor
  • Cell Movement / drug effects
  • Cell Movement / genetics
  • Cell Movement / physiology*
  • Chromones / pharmacology
  • Culture Media, Serum-Free / pharmacology
  • Cytoskeletal Proteins / metabolism
  • Enzyme Inhibitors / pharmacology
  • Female
  • Humans
  • Hydrogen-Ion Concentration
  • Immunoblotting
  • Integrin beta1 / metabolism
  • Membrane Proteins / metabolism
  • Microfilament Proteins / metabolism
  • Morpholines / pharmacology
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphorylation
  • Proto-Oncogene Proteins c-akt / antagonists & inhibitors
  • Proto-Oncogene Proteins c-akt / metabolism
  • Receptor, ErbB-2 / genetics
  • Receptor, ErbB-2 / metabolism*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction / drug effects
  • Sodium-Bicarbonate Symporters / antagonists & inhibitors
  • Sodium-Bicarbonate Symporters / genetics
  • Sodium-Bicarbonate Symporters / metabolism*
  • Sodium-Hydrogen Exchanger 1
  • Sodium-Hydrogen Exchangers / genetics
  • Sodium-Hydrogen Exchangers / metabolism*
  • Sulfonamides / pharmacology

Substances

  • Benzamides
  • Cation Transport Proteins
  • Chromones
  • Culture Media, Serum-Free
  • Cytoskeletal Proteins
  • Enzyme Inhibitors
  • Integrin beta1
  • Membrane Proteins
  • Microfilament Proteins
  • Morpholines
  • S 0859 compound
  • SLC4A7 protein, human
  • SLC9A1 protein, human
  • Sodium-Bicarbonate Symporters
  • Sodium-Hydrogen Exchanger 1
  • Sodium-Hydrogen Exchangers
  • Sulfonamides
  • ezrin
  • moesin
  • radixin
  • 2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one
  • Amiloride
  • Phosphatidylinositol 3-Kinases
  • Receptor, ErbB-2
  • Proto-Oncogene Proteins c-akt
  • ethylisopropylamiloride