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疱疹病毒作为溶瘤剂的分子基础。

The molecular basis of herpesviruses as oncolytic agents.

机构信息

Department of Experimental Pathology, University of Bologna, Bologna, Italy.

出版信息

Curr Pharm Biotechnol. 2012 Jul;13(9):1795-803. doi: 10.2174/138920112800958931.

Abstract

Herpes simplex viruses (HSVs) have entered clinical trials as oncolytic agents. The following properties make them good candidates. It is a mild pathogen; drugs (Aciclovir) are available to control viral infection; the large genome is amenable to genetic engineering, they can be rendered cancer-specific by deletion of genes, envelope glycoproteins allow the insertion of heterologous ligands to achieve modification of the natural tropism. Genetically modified HSVs have been thoroughly tested in humans. New generation recombinants retargeted to cancer-specific heterologous receptors have been generated and are presently evaluated in pre-clinical settings. They will be reviewed along with the molecular bases of cancer specificity and the strategies for the enhancement of oncolytic potential of HSV recombinants.

摘要

单纯疱疹病毒 (HSV) 已作为溶瘤剂进入临床试验。以下特性使它们成为理想的候选药物:它们是一种温和的病原体;有药物(阿昔洛韦)可用于控制病毒感染;其基因组较大,易于进行基因工程改造;通过删除基因,可以使它们具有肿瘤特异性;包膜糖蛋白允许插入异源配体,从而改变其自然趋向性。经过基因改造的单纯疱疹病毒已在人类中进行了充分的测试。现已生成并正在临床前环境中评估针对特定癌症的新型重组病毒,这些病毒针对特定的异源受体进行了靶向改造。本文将对这些病毒进行回顾,并讨论癌症特异性的分子基础,以及增强单纯疱疹病毒重组病毒溶瘤潜力的策略。

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