Journal of Neuro-Oncology

, Volume 88, Issue 2, pp 121–133

Knockdown of GluR1 expression by RNA interference inhibits glioma proliferation

  • John F. de Groot
  • Yuji Piao
  • Li Lu
  • Gregory N. Fuller
  • W. K. Alfred Yung
lab. investigation-human/animal tissue

DOI: 10.1007/s11060-008-9552-2

Cite this article as:
de Groot, J.F., Piao, Y., Lu, L. et al. J Neurooncol (2008) 88: 121. doi:10.1007/s11060-008-9552-2

Abstract

High-grade gliomas release excitotoxic concentrations of glutamate which contributes to their malignant phenotype. To improve our understanding of the mechanisms by which glutamate enhances tumor growth and invasion, we examined α-amino-3-hydroxy-5-methylisoxazole-4-propionic acid (AMPA)-mediated signaling in glioma cell lines. shRNA was used to stably knockdown GluR1, the most abundant AMPA receptor subunit in glioma, to evaluate its role in tumor signaling, proliferation and tumorigenicity. In a tissue array, there was a statistically significant increase in GluR1 expression in glioblastoma samples compared to anaplastic astrocytoma and low-grade tumors. In vitro, we observed a time and dose-dependent increase in MAPK phosphorylation following exposure to AMPA, which was blocked with AMPA receptor antagonists and the MEK1 inhibitor PD98059. Retroviral delivery of GluR1 shRNA in U251 and U87 glioma cells reduced GluR1 protein expression, inhibited AMPA-mediated increases in MAPK phosphorylation, and decreased glioma proliferation in vitro. U251 and U87 shGluR1 cells implanted into the flanks of nude mice grew slower than controls, which correlated with a decrease in proliferation measured by Ki-67 staining and an increase in apoptosis. These results suggest that AMPA receptors are abundantly expressed in high-grade gliomas and gene silencing of the GluR1 AMPA receptor subunit results in abrogation of AMPA-mediated signaling and tumor growth.

Keywords

Glioblastoma AMPA Receptors shRNA Glutamate Proliferation 

Copyright information

© Springer Science+Business Media, LLC. 2008

Authors and Affiliations

  • John F. de Groot
    • 1
    • 3
  • Yuji Piao
    • 1
  • Li Lu
    • 1
  • Gregory N. Fuller
    • 2
  • W. K. Alfred Yung
    • 1
  1. 1.Brain Tumor CenterThe University of Texas M. D. Anderson Cancer CenterHoustonUSA
  2. 2.Department of PathologyThe University of Texas M. D. Anderson Cancer CenterHoustonUSA
  3. 3.Department of Neuro-Oncology, Unit 431The University of Texas M. D. Anderson Cancer CenterHoustonUSA

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