Treatment of glial tumors with glutamate antagonists

Abstract

The present invention relates to a method of treating glial tumors in a subject, which includes providing a glutamate antagonist or a NMDA receptor antagonist and administering the glutamate antagonist or NMDA receptor antagonist to a subject with a glial tumor of the brain or spinal cord under conditions effective to treat the glial tumor.

Description

[0001] This application is a continuation of U.S. patent application Ser. No. 10 / 225,396, filed Aug. 20, 2002, which claims the benefit of U.S. Provisional Patent Application Ser. No. 60 / 313,030, filed Aug. 20, 2001, which are hereby incorporated by reference in their entirety.[0002] The subject matter of this application was made with support from the United States Government under grant numbers NS30007 and NS38073. The United States Government may have certain rights.FIELD OF THE INVENTION [0003] The present invention relates to the treatment of glial tumors in a living system by administering glutamate antagonists that modulate glutamate excitatory neurotransmitter function at ionotropic glutamate receptor complexes. BACKGROUND OF THE INVENTION [0004] Despite significant improvements in the early detection of malignant gliomas, the median survival of patients remains less than 12 months from the time of diagnosis (Benedetti et al., “Gene Therapy of Experimental Brain Tumors Using...

AI Technical Summary

Benefits of technology

[0011] The methods of the present invention provide for an improved treatment of glial tumors, a deadly set of cancers that are typically fatal within a year of diagnosis. In accordance with the present invention, glutamate antagonists, which inhibit the excitatory activity of glutamate, are administered in a manner which is effective to slow glial tumor expansion and, therefore, prolong the lives of patients with glial tumors. The methods of the present invention, based upon antagonizing glutamate secretion or its target receptors, demonstrate a new approach for treating brain tumors.

[0012] The present invention is directed to the use of glutamate antagonists in suppressing glial tumor expansion, and hence in treating CNS glial tumors, including astrocytoma and glioblastoma, and also their related neural and glial tumors, which include grades 1and 2 glioma, oligodendroglioma, neurocytoma, dysplastic neuroepithelial tumor, primitive neuroectodermal tumor, and ganglioneuroma. The use of glutamate antagonists in the treatment of systemic cancers has been otherwise proposed for non-brain tumors derived from cells known to be responsive to glutamate (European Patent Application Serial No. 1002535A1 to Ikonomidou, which is hereby incorporated by reference in its entirety). However, the use of glutamate antagonists in brain tumors is not taught or enabled (they studied neuroblastoma, which is derived from the peripheral nervous system, and not from the central nervous system). Further, Ikonomidou does not treat glial cell tumors (a non-metastatic tumor type), let alone does it do so in vivo. Rzeski et al., “Glutamate Antagonists Limit Tumor Growth,”Proc. Nat'l. Acad. Sci. USA 96(11):6372-77 (2001) extends this observation to the use of glutamate antagonists as cytotoxic agents for a number of cell lines, including breast carcinoma, colon carcinoma, adrenocarcinoma, thyroid carcinoma, rhabdomyosarcoma / medulloblastoma, astrocytoma, and neuroblastoma. In contrast, the present invention specifically teaches the use of glutamate antagonists as a means of suppressing the toxic effects of tumor-derived glutamate on surrounding brain cells. In this context, glutamate antagonists serve to inhibit the spread of tumor cells by preserving normal brain cells which would otherwise be damaged or killed by tumor-derived glutamate (Takano et al., Nature Med. 7:1010-15 (2001), which is hereby incorporated by reference in its entirety). This can be accomplished at much lower doses than those at which glutamate antagonists cause direct cytotoxicity (i.e. the mechanism used by Ikonomidou), thereby allowing the therapeutic use of glutamate antagonists at doses which are not associated with systemic toxicity. The present invention hereby teaches the in vivo therapeutic use of glutamate antagonists to treat brain cancer. The present invention takes advantage of the intimate association of normal glial cells with neurons, the glutamate-responsive excitable cell type of the adult brain. By suppressing neuronal activity and glutamate-associated neulronal loss and inflammation, glutamate antagonists may inhibit the spread of glial tumor cells into the affected region of neuronal loss, while concurrently contributing to the local preservation of neuronal viability (Takano et al., Nature Med. 7:1010-15 (2001), which is hereby incorporated by reference in its entirety).

Problems solved by technology

However, the use of glutamate antagonists in brain tumors is not taught or enabled (they studied neuroblastoma, which is derived from the peripheral nervous system, and not from the central nervous system).

Further, Ikonomidou does not treat glial cell tumors (a non-metastatic tumor type), let alone does it do so in vivo.

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