Chemokine receptor CXCR4-mediated transformation of mammary epithelial cells by enhancing multiple RTKs expression and deregulation of the p53/MDM2 axis

Cancer Lett. 2011 Aug 28;307(2):132-40. doi: 10.1016/j.canlet.2011.03.025. Epub 2011 May 6.

Abstract

Recent studies have shown that CXCR4 is associated with tumor metastasis. Elevated levels of CXCR4 are also detected in a high percentage of DCIS cases. The high frequency of CXCR4 expression in DCIS suggests that many DCIS cases are "primed" for invasiveness. In this study, we demonstrated that expression of CXCR4 reveals morphological alterations in cells, from normal acinar morphological epithelial cells to a more invasive morphology in a 3D-culture system. Ectopic expression of CXCR4 induces invasion of MCF-10A cells. Interestingly, CXCR4 is capable of orchestrating a complex alteration in signaling networks, which include upregulation of multiple receptor tyrosine kinases (RTKs), deregulation of p53/MDM2 axis, upregulation of E-cadherin and c-myc, as well as modulation of cell cycle molecules to facilitate mammary epithelia cell transformation. These findings reveal that CXCR4 expression exerts a critical role in early stages of breast lesions, which may explain the high frequency of CXCR4 expression detected in DCIS. We believe that these studies will lead to new, biologically-based therapeutic strategies for clinical intervention, prevention and treatments of breast cancer.

Publication types

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

MeSH terms

  • Base Sequence
  • Cell Line, Transformed
  • Cell Transformation, Neoplastic*
  • DNA Primers
  • Flow Cytometry
  • Humans
  • Mammary Glands, Human / pathology*
  • Proto-Oncogene Proteins c-mdm2 / metabolism*
  • Receptor Protein-Tyrosine Kinases / metabolism*
  • Receptors, CXCR4 / physiology*
  • Tumor Suppressor Protein p53 / metabolism*

Substances

  • CXCR4 protein, human
  • DNA Primers
  • Receptors, CXCR4
  • Tumor Suppressor Protein p53
  • MDM2 protein, human
  • Proto-Oncogene Proteins c-mdm2
  • Receptor Protein-Tyrosine Kinases