4.6 Article

Poliovirus receptor CD155-targeted oncolysis of glioma

Journal

NEURO-ONCOLOGY
Volume 6, Issue 3, Pages 208-217

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1215/S1152851703000577

Keywords

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Funding

  1. NCI NIH HHS [R37 CA011898, R01 CA087537, CA11898, P20 CA096890, R55 CA087537, CA87537] Funding Source: Medline
  2. NCRR NIH HHS [M01 RR 30] Funding Source: Medline
  3. NINDS NIH HHS [P50 NS020023, NS20023] Funding Source: Medline

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Cell adhesion molecules of the immunoglobulin superfamily are aberrantly expressed in malignant glioma. Amongst these, the human poliovirus receptor CD155 provides a molecular target for therapeutic intervention with oncolytic poliovirus recombinants. Poliovirus has been genetically modified through insertion of regulatory sequences derived from human rhinovirus type 2 to selectively replicate within and destroy cancerous cells. Efficacious oncolysis mediated by poliovirus derivatives depends on the presence of CD155 in targeted tumors. To prepare oncolytic polioviruses for clinical application, we have developed a series of assays in high-grade malignant glioma (HGL) to characterize CD155 expression levels and susceptibility to oncolytic poliovirus recombinants. Analysis of 6 HGL cases indicates that CD155 is expressed in these tumors and in primary cell lines derived from these tumors. Upregulation of the molecular target CD155 rendered explant cultures of all studied tumors highly susceptible to a prototype oncolytic poliovirus recombinant. Our observations support the clinical application of such agents against HGL.

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