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基因治疗的局部递送

Local delivery for gene therapy.

作者信息

Clayman G L, Dreiling L

机构信息

Department of Cancer Biology, University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Box 69, Houston, TX 77030, USA.

出版信息

Curr Oncol Rep. 1999;1(2):138-43. doi: 10.1007/s11912-999-0024-4.

Abstract

Patients with head and neck cancers are excellent candidates for gene therapy. With few effective alternatives for patients with recurrent or locally metastatic disease, gene therapy offers a new approach for local control and the possibility to enhance other treatment modalities as well. Different therapeutic genes, including tumor suppressor genes, prodrug or suicide genes, and genes whose products enhance immunocompetence, can be delivered using specifically designed vectors with little toxicity or threat of undesirable viral spread. Two of these gene therapy agents, RPR/INGN 201 and HLA-B7 + beta2 microglobulin, have shown clinical activity, according to reports from phase I trials.

摘要

头颈癌患者是基因治疗的理想对象。对于复发或局部转移性疾病患者而言,有效替代方案寥寥无几,基因治疗为局部控制提供了一种新方法,还有可能增强其他治疗方式的效果。不同的治疗基因,包括肿瘤抑制基因、前体药物或自杀基因,以及其产物可增强免疫能力的基因,可通过专门设计的载体进行递送,且毒性极小,也不存在不良病毒传播的风险。根据一期试验报告,其中两种基因治疗药物,即RPR/INGN 201和HLA - B7 + β2微球蛋白,已显示出临床活性。

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