Merrill Melinda K, Bernhardt Guenter, Sampson John H, Wikstrand Carol J, Bigner Darell D, Gromeier Matthias
Department of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, NC 27710, USA.
Neuro Oncol. 2004 Jul;6(3):208-17. doi: 10.1215/S1152851703000577.
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.
免疫球蛋白超家族的细胞黏附分子在恶性胶质瘤中异常表达。其中,人脊髓灰质炎病毒受体CD155为溶瘤性脊髓灰质炎病毒重组体的治疗干预提供了一个分子靶点。脊髓灰质炎病毒已通过插入源自人鼻病毒2型的调控序列进行基因改造,以在癌细胞内选择性复制并破坏癌细胞。脊髓灰质炎病毒衍生物介导的有效溶瘤作用取决于靶向肿瘤中CD155的存在。为了制备用于临床应用的溶瘤性脊髓灰质炎病毒,我们在高级别恶性胶质瘤(HGL)中开发了一系列检测方法,以表征CD155的表达水平以及对溶瘤性脊髓灰质炎病毒重组体的敏感性。对6例HGL病例的分析表明,CD155在这些肿瘤以及源自这些肿瘤的原代细胞系中表达。分子靶点CD155的上调使所有研究肿瘤的外植体培养物对原型溶瘤性脊髓灰质炎病毒重组体高度敏感。我们的观察结果支持此类药物针对HGL的临床应用。