Chromatin-associated CSF-1R binds to the promoter of proliferation-related genes in breast cancer cells

Oncogene. 2014 Aug 21;33(34):4359-64. doi: 10.1038/onc.2013.542. Epub 2013 Dec 23.

Abstract

The colony-stimulating factor-1 (CSF-1) and its receptor CSF-1R physiologically regulate the monocyte/macrophage system, trophoblast implantation and breast development. An abnormal CSF-1R expression has been documented in several human epithelial tumors, including breast carcinomas. We recently demonstrated that CSF-1/CSF-1R signaling drives proliferation of breast cancer cells via 'classical' receptor tyrosine kinase signaling, including activation of the extracellular signal-regulated kinase 1/2. In this paper, we show that CSF-1R can also localize within the nucleus of breast cancer cells, either cell lines or tissue specimens, irrespectively of their intrinsic molecular subtype. We found that the majority of nuclear CSF-1R is located in the chromatin-bound subcellular compartment. Chromatin immunoprecipitation revealed that CSF-1R, once in the nucleus, binds to the promoters of the proliferation-related genes CCND1, c-JUN and c-MYC. CSF-1R also binds the promoter of its ligand CSF-1 and positively regulates CSF-1 expression. The existence of such a receptor/ligand regulatory loop is a novel aspect of CSF-1R signaling. Moreover, our results provided the first evidence of a novel localization site of CSF-1R in breast cancer cells, suggesting that CSF-1R could act as a transcriptional regulator on proliferation-related genes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Breast Neoplasms / metabolism*
  • Breast Neoplasms / pathology
  • Cell Line, Tumor
  • Cell Nucleus / metabolism
  • Cell Proliferation*
  • Chromatin / metabolism*
  • Feedback, Physiological
  • Female
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Mice
  • NIH 3T3 Cells
  • Promoter Regions, Genetic*
  • Protein Binding
  • Protein Transport
  • Receptor, Macrophage Colony-Stimulating Factor / metabolism*
  • Signal Transduction
  • Solubility
  • Transcription, Genetic

Substances

  • Chromatin
  • Receptor, Macrophage Colony-Stimulating Factor