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基于腺病毒的癌症基因治疗的现状

The current status of adenovirus-based cancer gene therapy.

作者信息

Shirakawa Toshiro

机构信息

International Center for Medical Research and Treatment (ICMRT), Kobe University School of Medicine, Kobe 650-0017, Japan.

出版信息

Mol Cells. 2008 Jun 30;25(4):462-6. Epub 2008 May 6.

Abstract

Adenoviruses are the most commonly used gene-delivery vectors due to the efficiency of their in vivo gene transfer. Since 1993, about 300 protocols using an adenoviral vector have been performed, although they have yet to be proven effective in clinical trials. The adenovirus-based vector has been continuously improved by modification of the adenoviral genome and capsid, and novel adenovirus-delivery systems, such as the carrier-cell delivery system, have been recently proposed. Adenovirus-based cancer gene therapy is fast becoming one component of a multi-modality treatment approach to advanced cancer, along with surgery, radiotherapy, and chemotherapy.

摘要

由于腺病毒在体内基因转移方面的高效性,它们是最常用的基因递送载体。自1993年以来,已经进行了约300项使用腺病毒载体的实验方案,尽管它们在临床试验中尚未被证明有效。基于腺病毒的载体通过对腺病毒基因组和衣壳的修饰而不断改进,并且最近还提出了新型腺病毒递送系统,如载体细胞递送系统。基于腺病毒的癌症基因治疗正迅速成为晚期癌症多模态治疗方法的一个组成部分,与手术、放疗和化疗一起。

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