Targeting hyaluronan interactions in spinal cord astrocytomas and diffuse pontine gliomas

J Child Neurol. 2008 Oct;23(10):1214-20. doi: 10.1177/0883073808321771.

Abstract

Although significant advances have been made in treating malignant pediatric central nervous system tumors such as medulloblastoma, no effective therapy exists for diffuse pontine glioma or intramedullary spinal astrocytoma. Biology of these 2 tumors is poorly understood, in part because diffuse pontine gliomas are not treated surgically, and tumor specimens from intramedullary spinal astrocytomas are rare and minuscule. At the 2007 Neurobiology of Disease in Children Symposium, we presented evidence that malignant glioma behaviors, including antiapoptosis, invasiveness, and treatment resistance, are enhanced by hyaluronan, an extracellular glycosaminoglycan. We review the clinical course of pediatric intramedullary spinal astrocytoma and diffuse pontine glioma, and show expression of membrane proteins that interact with hyaluronan: CD44, extracellular matrix metalloproteinase inducer, and breast cancer resistance protein (BCRP/ABCG2). Furthermore, we describe novel animal models of these tumors for preclinical studies. These findings suggest that hyaluronan antagonism has potential therapeutic value in malignant central nervous system tumors.

Publication types

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

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily G, Member 2
  • ATP-Binding Cassette Transporters / genetics
  • ATP-Binding Cassette Transporters / metabolism
  • Animals
  • Astrocytoma / drug therapy
  • Astrocytoma / metabolism*
  • Astrocytoma / physiopathology
  • Basigin / genetics
  • Basigin / metabolism
  • Brain Stem Neoplasms / drug therapy
  • Brain Stem Neoplasms / metabolism*
  • Brain Stem Neoplasms / physiopathology
  • Child
  • Disease Models, Animal
  • Drug Resistance, Neoplasm / genetics
  • Glioma / drug therapy
  • Glioma / metabolism*
  • Glioma / physiopathology
  • Humans
  • Hyaluronan Receptors / genetics
  • Hyaluronan Receptors / metabolism
  • Hyaluronic Acid / genetics
  • Hyaluronic Acid / metabolism*
  • Neoplasm Proteins / genetics
  • Neoplasm Proteins / metabolism
  • Rats
  • Spinal Cord Neoplasms / drug therapy
  • Spinal Cord Neoplasms / metabolism*
  • Spinal Cord Neoplasms / physiopathology

Substances

  • ABCG2 protein, human
  • ATP Binding Cassette Transporter, Subfamily G, Member 2
  • ATP-Binding Cassette Transporters
  • BSG protein, human
  • Hyaluronan Receptors
  • Neoplasm Proteins
  • Basigin
  • Hyaluronic Acid