Inhibition of Fatty Acid Synthase Decreases Expression of Stemness Markers in Glioma Stem Cells

PLoS One. 2016 Jan 25;11(1):e0147717. doi: 10.1371/journal.pone.0147717. eCollection 2016.

Abstract

Cellular metabolic changes, especially to lipid metabolism, have recently been recognized as a hallmark of various cancer cells. However, little is known about the significance of cellular lipid metabolism in the regulation of biological activity of glioma stem cells (GSCs). In this study, we examined the expression and role of fatty acid synthase (FASN), a key lipogenic enzyme, in GSCs. In the de novo lipid synthesis assay, GSCs exhibited higher lipogenesis than differentiated non-GSCs. Western blot and immunocytochemical analyses revealed that FASN is strongly expressed in multiple lines of patient-derived GSCs (G144 and Y10), but its expression was markedly reduced upon differentiation. When GSCs were treated with 20 μM cerulenin, a pharmacological inhibitor of FASN, their proliferation and migration were significantly suppressed and de novo lipogenesis decreased. Furthermore, following cerulenin treatment, expression of the GSC markers nestin, Sox2 and fatty acid binding protein (FABP7), markers of GCSs, decreased while that of glial fibrillary acidic protein (GFAP) expression increased. Taken together, our results indicate that FASN plays a pivotal role in the maintenance of GSC stemness, and FASN-mediated de novo lipid biosynthesis is closely associated with tumor growth and invasion in glioblastoma.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects
  • Cerulenin / pharmacology
  • Fatty Acid Synthases / antagonists & inhibitors
  • Fatty Acid Synthases / metabolism*
  • Female
  • Gene Expression Regulation, Neoplastic*
  • Glioma / enzymology*
  • Glioma / metabolism*
  • Humans
  • Male
  • Middle Aged
  • Neoplastic Stem Cells / cytology
  • Neoplastic Stem Cells / metabolism*
  • Tumor Cells, Cultured

Substances

  • Cerulenin
  • Fatty Acid Synthases

Grants and funding

The authors have no support or funding to report.