Upregulation of CXCR4 is essential for HER2-mediated tumor metastasis

Cancer Cell. 2004 Nov;6(5):459-69. doi: 10.1016/j.ccr.2004.09.027.

Abstract

The receptor tyrosine kinase HER2 enhances tumor metastasis; however, its role in homing to metastatic organs is poorly understood. The chemokine receptor CXCR4 has recently been shown to mediate the movement of malignant cancer cells to specific organs. Here, we show that HER2 enhances the expression of CXCR4, which is required for HER2-mediated invasion in vitro and lung metastasis in vivo. HER2 also inhibits ligand-induced CXCR4 degradation. Finally, a significant correlation between HER2 and CXCR4 expression was observed in human breast tumor tissues, and CXCR4 expression correlated with a poor overall survival rate in patients with breast cancer. These results provide a plausible mechanism for HER2-mediated breast tumor metastasis and establish a functional link between HER2 and CXCR4 signaling pathways.

Publication types

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

MeSH terms

  • Animals
  • Breast Neoplasms / metabolism*
  • Breast Neoplasms / pathology*
  • Humans
  • Ligands
  • Lung Neoplasms / secondary
  • Mice
  • NIH 3T3 Cells
  • Neoplasm Metastasis
  • Receptor, ErbB-2 / physiology*
  • Receptors, CXCR4 / metabolism*
  • Transfection
  • Tumor Cells, Cultured
  • Up-Regulation*

Substances

  • Ligands
  • Receptors, CXCR4
  • Receptor, ErbB-2