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利用多样性:创建高效且有效的溶瘤病毒的遗传方法。

Exploiting diversity: genetic approaches to creating highly potent and efficacious oncolytic viruses.

作者信息

Bauzon Maxine, Hermiston Terry W

机构信息

Bayer Healthcare, Pharmaceuticals Division, Novel Technologies Department, 2600 Hilltop Drive, Richmond, CA 94806, USA.

出版信息

Curr Opin Mol Ther. 2008 Aug;10(4):350-5.

Abstract

Oncolytic viruses possess several key attributes that make them a highly attractive treatment for cancer. They exhibit clinically validated synergy with chemotherapy and an ability to selectively destroy tumor cells to the exclusion of normal cells. Oncolytic viruses can replicate and, therefore, amplify their dose in a tumor-dependent manner. In addition, they can be genetically manipulated to include additional therapeutic factors to create a multimodal anticancer agent. These characteristics lead to the expectation that oncolytic viruses will serve as an additional tool in the treatment repertoire of clinical oncologists. In their clinical development to date, these agents were safe and well tolerated, but lacked efficacy as monotherapies. In this review, three genetic-based methods to increase the potency and efficacy of oncolytic viruses, in which human adenovirus is utilized as an example of a prototype oncolytic virus, are discussed.

摘要

溶瘤病毒具有几个关键特性,使其成为极具吸引力的癌症治疗手段。它们与化疗展现出经过临床验证的协同作用,并且具备选择性破坏肿瘤细胞而不影响正常细胞的能力。溶瘤病毒能够复制,因此可以以肿瘤依赖的方式扩大其剂量。此外,它们可以通过基因操作加入额外的治疗因子,从而打造一种多模式抗癌药物。这些特性使得人们期望溶瘤病毒将成为临床肿瘤学家治疗方案中的又一工具。在其迄今为止的临床开发中,这些药物安全性良好且耐受性佳,但作为单一疗法缺乏疗效。在本综述中,讨论了三种基于基因的提高溶瘤病毒效力和疗效的方法,其中以人腺病毒作为原型溶瘤病毒的示例。

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