Smith E R, Chiocca E A
Molecular Neuro-oncology Laboratories, Neurosurgery Service, Massachusetts General Hospital, CNY6, 13th Street, Charlestown, MA 02119, USA.
Expert Opin Investig Drugs. 2000 Feb;9(2):311-27. doi: 10.1517/13543784.9.2.311.
Although the use of viruses as oncolytic agents is an historic concept, the use of genetically modified viruses to selectively target tumour cells is relatively novel and recent. The ability of viruses to efficiently infect and lyse cells, combined with the potential augmentation of this effect by progeny viruses throughout the tumour provide justification for exploitation of these agents in cancer therapy. Before application to humans, though, issues related to tumour cell selectivity, lack of toxicity to normal tissues and the effect of the antiviral immune response, will have to be clarified. The more commonly used oncolytic viruses are based on mutant strains of herpes simplex virus, adenovirus and reovirus. The tumour selectivity of each of these strains is discussed, particularly the complementation of the viral defect by cellular pathways involved in tumourigenesis. The combination of oncolytic viruses with radiation, chemotherapy and gene therapy is also reviewed. Further study of the interaction of viral proteins with cellular pathways involved in cell cycle control will provide the rationale for viral mutants with increased selectivity for tumour cells.
尽管将病毒用作溶瘤剂是一个由来已久的概念,但利用基因改造病毒来选择性靶向肿瘤细胞则相对新颖且为时不久。病毒高效感染和裂解细胞的能力,以及子代病毒在整个肿瘤中对这种效应的潜在增强作用,为在癌症治疗中利用这些制剂提供了依据。不过,在应用于人类之前,与肿瘤细胞选择性、对正常组织无毒性以及抗病毒免疫反应的影响相关的问题必须得到阐明。更常用的溶瘤病毒基于单纯疱疹病毒、腺病毒和呼肠孤病毒的突变株。本文讨论了这些毒株各自的肿瘤选择性,特别是参与肿瘤发生的细胞途径对病毒缺陷的互补作用。还综述了溶瘤病毒与放射疗法、化学疗法和基因疗法的联合应用。对病毒蛋白与参与细胞周期控制的细胞途径之间相互作用的进一步研究,将为对肿瘤细胞具有更高选择性的病毒突变体提供理论依据。