Centre for Molecular Oncology, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom ; Department of Otolaryngology, Cambridge University Hospitals, Cambridge, United Kingdom ; Sino-British Research Center for Molecular Oncology, Zhengzhou University, Zhengzhou, People's Republic of China.
Onco Targets Ther. 2013 Jul 31;6:1031-40. doi: 10.2147/OTT.S46974. Print 2013.
Oncolytic viruses (OVs) have the ability to selectively replicate in and lyse cancer cells. Angiogenesis is an essential requirement for tumor growth. Like OVs, the therapeutic effect of many angiogenesis inhibitors has been limited, leading to the development of more effective approaches to combine antiangiogenic therapy with OVs. Angiogenesis can be targeted either directly by OV infection of vascular endothelial cells, or by arming OVs with antiangiogenic transgenes, which are subsequently expressed locally in the tumor microenvironment. In this review, we describe the development and targeting of OVs, the role of angiogenesis in cancer, and the progress made in arming viruses with antiangiogenic transgenes. Future developments required to optimize this approach are addressed.
溶瘤病毒(OVs)具有在癌细胞中选择性复制和裂解的能力。血管生成是肿瘤生长的必要条件。与 OVs 类似,许多血管生成抑制剂的治疗效果受到限制,这导致开发更有效的方法将抗血管生成治疗与 OVs 结合。血管生成可以通过 OV 感染血管内皮细胞直接靶向,也可以通过用抗血管生成转基因武装 OVs 来靶向,这些转基因随后在肿瘤微环境中局部表达。在这篇综述中,我们描述了 OVs 的开发和靶向、血管生成在癌症中的作用以及用抗血管生成转基因武装病毒所取得的进展。解决了优化这种方法所需的未来发展。