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逆转录病毒介导的基因转移至肿瘤:利用病毒的复制能力在体内实现高效的肿瘤转导。

Retrovirus-mediated gene transfer to tumors: utilizing the replicative power of viruses to achieve highly efficient tumor transduction in vivo.

作者信息

Logg Christopher R, Kasahara Noriyuki

机构信息

Department of Medicine, School of Medicine, University of California, Los Angeles, CA, USA.

出版信息

Methods Mol Biol. 2004;246:499-525. doi: 10.1385/1-59259-650-9:499.

Abstract

Vectors derived from retroviruses have been widely studied as tools for gene transfer into mammalian tissue in vivo. One application for which retroviral vectors have received particular attention is gene transfer into tumor cells for treatment of cancer. Simple retroviruses, such as murine leukemia virus (MLV), and the vectors derived from them, require cell division for infection and thus possess a degree of inherent specificity for the rapidly dividing cells of neoplastic tissue. This unique property and the ease with which retroviral vectors are manipulated and produced have provided much of the impetus for their use in experimental and clinical cancer gene-therapy studies.

摘要

源自逆转录病毒的载体作为将基因导入哺乳动物体内组织的工具已得到广泛研究。逆转录病毒载体受到特别关注的一个应用是将基因导入肿瘤细胞以治疗癌症。简单的逆转录病毒,如鼠白血病病毒(MLV)及其衍生的载体,需要细胞分裂才能进行感染,因此对肿瘤组织中快速分裂的细胞具有一定程度的内在特异性。这种独特的性质以及逆转录病毒载体易于操作和生产的特点,为其在实验性和临床癌症基因治疗研究中的应用提供了很大的推动力。

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