溶瘤病毒
单纯疱疹病毒
溶癌病毒
病毒学
向性
HSL和HSV色彩空间
病毒
载体(分子生物学)
生物
病毒复制
癌症研究
基因
重组DNA
遗传学
作者
Hiroaki Uchida,Hirofumi Hamada,Kenji Nakano,Heechung Kwon,Hideaki Tahara,Justus B. Cohen,Joseph C. Glorioso
出处
期刊:Current Cancer Drug Targets
[Bentham Science]
日期:2018-01-15
卷期号:18 (2): 162-170
被引量:21
标识
DOI:10.2174/1568009617666170206105855
摘要
Oncolytic virotherapy is a novel therapeutic modality for malignant diseases that exploits selective viral replication in cancer cells. Herpes simplex virus (HSV) is a promising agent for oncolytic virotherapy due to its broad cell tropism and the identification of mutations that favor its replication in tumor over normal cells. However, these attenuating mutations also tend to limit the potency of current oncolytic HSV vectors that have entered clinical studies. As an alternative, vector retargeting to novel entry receptors has the potential to achieve tumor specificity at the stage of virus entry, eliminating the need for replication-attenuating mutations. Here, we summarize the molecular mechanism of HSV entry and recent advances in the development of fully retargeted HSV vectors for oncolytic virotherapy. Retargeted HSV vectors offer an attractive platform for the creation of a new generation of oncolytic HSV with improved efficacy and specificity.
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