控制腺病毒复制诱导溶瘤效果

C. Fillat, Anabel José, X. B. Ros, A. Mato-Berciano, M. V. Maliandi, D. Abate-Daga
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引用次数: 4

摘要

在过去的十年中,癌症治疗发现自己受到了日益增长的溶瘤病毒治疗领域的挑战。许多不同的病毒目前正在研究中,研究它们通过病毒感染和细胞裂解的重复循环诱导抗肿瘤作用的潜力。然而,基因工程复制选择性腺病毒是第一个进入癌症患者临床试验的。在单个溶瘤腺病毒中结合选择性和提高效力的困难促使研究人员设计和测试了许多不同的方法。本文介绍了基于病毒复制控制的不同策略。我们讨论了细胞和肿瘤生物学知识的增长,以及腺病毒病毒学的进步,如何激发了基因工程腺病毒的微调。特别强调使用某些特定遗传元素背后的基础,引入病毒基因组以控制病毒基因表达,并描述最重要的病毒基因突变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Controlling Adenoviral Replication to Induce Oncolytic Efficacy
Over the last decade, cancer therapy has found itself challenged by the growing field of oncolytic virotherapy. Many different viruses are currently under study, investigating their potential to induce antitumor effects through repeated cycles of viral infection and cell lysis. It was, however, genetically-engineered replication-selective adenoviruses that were the first to enter clinical trials with cancer patients. The difficulties involved in combining selectivity and elevated potency in a single oncolytic adenovirus have led investigators to design and test many different approaches. Different strategies, based on the control of viral replication, are presented in the current review. We discuss how the growing knowledge of cell and tumour biology, with the advances made in adenoviral virology, has inspired the fine-tuning of genetically-engineered adenoviruses. Special emphasis is placed on the fundamentals behind the use of certain specific genetic elements, introduced into the viral genome to control viral gene expression and on describing the most important viral gene mutations.
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