Why the study?
Does a prototype oncolytic poliovirus recombinant target and destroy high-grade malignant glioma cells expressing CD155?
Does a prototype oncolytic poliovirus recombinant target and destroy high-grade malignant glioma cells expressing CD155?
High-grade malignant gliomas express CD155, making them highly susceptible to targeted oncolysis by genetically modified poliovirus recombinants in preclinical models.
Answers are grounded in this paper and cite their sources.
Supports poliovirus oncolytic development in CD155+ gliomas; leaves open translation to clinical trials.
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.
No takes yet. Share an insight, caveat, or question.
Merrill et al. (2004) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: