This Article Full Text Full Text (PDF) Correction (v67,p10624) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Lyons, S. A. Articles by Sontheimer, H. Search for Related Content PubMed PubMed Citation Articles by Lyons, S. A. Articles by Sontheimer, H.

Autocrine Glutamate Signaling Promotes Glioma Cell Invasion

Department of Neurobiology, Center for Glial Biology in Medicine, University of Alabama at Birmingham, Birmingham, Alabama

Requests for reprints: Harald Sontheimer, Center for Glial Biology in Medicine, University of Alabama at Birmingham, 1719 6th Avenue South CIRC 410, Birmingham, AL 35294. Phone: 205-975-5805; E-mail: Sontheimer{at}uab.edu.

Malignant gliomas have been shown to release glutamate, which kills surrounding brain cells, creating room for tumor expansion. This glutamate release occurs primarily via system x_C^–, a Na⁺-independent cystine-glutamate exchanger. We show here, in addition, that the released glutamate acts as an essential autocrine/paracrine signal that promotes cell invasion. Specifically, chemotactic invasion and scrape motility assays each show dose-dependent inhibition of cell migration when glutamate release was inhibited using either S-(4)-CPG or sulfasalazine, both potent blockers of system x_C^–. This inhibition could be overcome by the addition of exogenous glutamate (100 µmol/L) in the continued presence of the inhibitors. Migration/invasion was also inhibited when Ca²⁺-permeable -amino-3-hydroxy-5-methylisoxazole-4-propionic acid receptors (AMPA-R) were blocked using GYKI or Joro spider toxin, whereas CNQX was ineffective. Ca²⁺ imaging experiments show that the released glutamate activates Ca²⁺-permeable AMPA-R and induces intracellular Ca²⁺ oscillations that are essential for cell migration. Importantly, glioma cells release glutamate in sufficient quantities to activate AMPA-Rs on themselves or neighboring cells, thus acting in an autocrine and/or paracrine fashion. System x_C^– and the appropriate AMPA-R subunits are expressed in all glioma cell lines, patient-derived glioma cells, and acute patient biopsies investigated. Furthermore, animal studies in which human gliomas were xenographed into scid mice show that chronic inhibition of system x_C^––mediated glutamate release leads to smaller and less invasive tumors compared with saline-treated controls. These data suggest that glioma invasion is effectively disrupted by inhibiting an autocrine glutamate signaling loop with a clinically approved candidate drug, sulfasalazine, already in hand. [Cancer Res 2007;67(19):9463–71]

This article has been cited by other articles:

				H. Sontheimer An Unexpected Role for Ion Channels in Brain Tumor Metastasis Experimental Biology and Medicine, July 1, 2008; 233(7): 779 - 791. [Abstract] [Full Text] [PDF]

				Correction: Autocrine Glutamate Signals Promote Glioma Invasion Cancer Res., November 1, 2007; 67(21): 10624 - 10624. [Full Text] [PDF]