4.6 Article

Poliovirus receptor CD155-targeted oncolysis of glioma

期刊

NEURO-ONCOLOGY
卷 6, 期 3, 页码 208-217

出版社

OXFORD UNIV PRESS INC
DOI: 10.1215/S1152851703000577

关键词

-

资金

  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

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据