Ossifying fibroma tumor stem cells are maintained by epigenetic regulation of a TSP1/TGF-β/SMAD3 autocrine loop

Cell Stem Cell. 2013 Nov 7;13(5):577-89. doi: 10.1016/j.stem.2013.08.010.

Abstract

Abnormal stem cell function makes a known contribution to many malignant tumors, but the role of stem cells in benign tumors is not well understood. Here, we show that ossifying fibroma (OF) contains a stem cell population that resembles mesenchymal stem cells (OFMSCs) and is capable of generating OF-like tumor xenografts. Mechanistically, OFMSCs show enhanced TGF-β signaling that induces aberrant proliferation and deficient osteogenesis via Notch and BMP signaling pathways, respectively. The elevated TGF-β activity is tightly regulated by JHDM1D-mediated epigenetic regulation of thrombospondin-1 (TSP1), forming a JHDM1D/TSP1/TGF-β/SMAD3 autocrine loop. Inhibition of TGF-β signaling in OFMSCs can rescue their abnormal osteogenic differentiation and elevated proliferation rate. Furthermore, chronic activation of TGF-β can convert normal MSCs into OF-like MSCs via establishment of this JHDM1D/TSP1/TGF-β/SMAD3 autocrine loop. These results reveal that epigenetic regulation of TGF-β signaling in MSCs governs the benign tumor phenotype in OF and highlight TGF-β signaling as a candidate therapeutic target.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Retracted Publication

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors / genetics*
  • Epigenesis, Genetic / genetics*
  • Fibroma, Ossifying / metabolism*
  • Fibroma, Ossifying / pathology*
  • Humans
  • Mice
  • Neoplastic Stem Cells* / cytology
  • Neoplastic Stem Cells* / metabolism
  • Smad3 Protein / genetics*
  • Transforming Growth Factor beta / genetics*

Substances

  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
  • SPZ1 protein, human
  • Smad3 Protein
  • Transforming Growth Factor beta

Associated data

  • GEO/GSE49165