Proteoglycans and their roles in brain cancer

FEBS J. 2013 May;280(10):2399-417. doi: 10.1111/febs.12109. Epub 2013 Feb 6.

Abstract

Glioblastoma, a malignant brain cancer, is characterized by abnormal activation of receptor tyrosine kinase signalling pathways and a poor prognosis. Extracellular proteoglycans, including heparan sulfate and chondroitin sulfate, play critical roles in the regulation of cell signalling and migration via interactions with extracellular ligands, growth factor receptors and extracellular matrix components, as well as intracellular enzymes and structural proteins. In cancer, proteoglycans help drive multiple oncogenic pathways in tumour cells and promote critical tumour-microenvironment interactions. In the present review, we summarize the evidence for proteoglycan function in gliomagenesis and examine the expression of proteoglycans and their modifying enzymes in human glioblastoma using data obtained from The Cancer Genome Atlas (http://cancergenome.nih.gov/). Furthermore, we demonstrate an association between specific proteoglycan alterations and changes in receptor tyrosine kinases. Based on these data, we propose a model in which proteoglycans and their modifying enzymes promote receptor tyrosine kinase signalling and progression in glioblastoma, and we suggest that cancer-associated proteoglycans are promising biomarkers for disease and therapeutic targets.

Publication types

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

MeSH terms

  • Animals
  • Brain Neoplasms / metabolism
  • Brain Neoplasms / pathology*
  • Cell Movement
  • ErbB Receptors / genetics
  • ErbB Receptors / metabolism
  • Extracellular Matrix / metabolism
  • Extracellular Matrix / pathology
  • Gene Expression Regulation, Neoplastic*
  • Glioblastoma / metabolism
  • Glioblastoma / pathology
  • Humans
  • Inflammation / metabolism
  • Inflammation / pathology
  • Neovascularization, Pathologic / metabolism
  • Neovascularization, Pathologic / pathology
  • Proteoglycans / genetics
  • Proteoglycans / metabolism*
  • Receptor, Platelet-Derived Growth Factor alpha / genetics
  • Receptor, Platelet-Derived Growth Factor alpha / metabolism
  • Signal Transduction
  • Sulfatases
  • Sulfotransferases / genetics
  • Sulfotransferases / metabolism
  • Tumor Microenvironment

Substances

  • Proteoglycans
  • EGFR protein, human
  • ErbB Receptors
  • Receptor, Platelet-Derived Growth Factor alpha
  • Sulfotransferases
  • SULF2 protein, human
  • Sulfatases