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超声增强化疗及向胶质瘤细胞的基因递送

Ultrasound-enhanced chemotherapy and gene delivery for glioma cells.

作者信息

Zarnitsyn Vladimir G, Kamaev Pavel P, Prausnitz Mark R

机构信息

School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, 315 Ferst Drive, Atlanta, GA 30332-0100, USA.

出版信息

Technol Cancer Res Treat. 2007 Oct;6(5):433-42. doi: 10.1177/153303460700600509.

Abstract

Treatment of brain cancer is limited in part by inefficient intracellular delivery of drugs and DNA for chemotherapy and gene therapy, respectively. This study tested the hypothesis that ultrasound may be used to enhance intracellular delivery and efficacy of chemotherapeutics and genes in glioma cells in vitro. First, suitable ultrasound conditions were identified by measuring intracellular uptake of calcein and viability of GS 9L rat gliosarcoma cells after a range of different ultrasound exposures. We selected sonication at 10 J/cm2, which achieved intracellular delivery of approximately 10(6) molecules/cell. Next, glial cells were sonicated with varying concentrations of model chemotherapeutics: BCNU and bleomycin. For both drugs, cytotoxicity was increased in a synergistic manner when accompanied by ultrasound exposure. Finally, expression of a plasmid DNA encoding a GFP reporter was increased up to 30-fold when exposed to ultrasound. Altogether, these findings suggest that ultrasound may be useful to increase the efficacy of chemotherapy and gene therapy of glioma cells.

摘要

脑癌治疗在一定程度上受到限制,原因分别是用于化疗的药物和用于基因治疗的DNA在细胞内递送效率低下。本研究检验了一个假设,即超声可用于增强化疗药物和基因在体外胶质瘤细胞中的细胞内递送及疗效。首先,通过测量一系列不同超声照射后钙黄绿素的细胞内摄取量以及GS 9L大鼠胶质肉瘤细胞的活力,确定了合适的超声条件。我们选择了10 J/cm2的超声处理,其实现了约10(6)个分子/细胞的细胞内递送。接下来,用不同浓度的模型化疗药物:卡莫司汀(BCNU)和博来霉素对神经胶质细胞进行超声处理。对于这两种药物,当伴有超声照射时,细胞毒性以协同方式增加。最后,当暴露于超声时,编码绿色荧光蛋白(GFP)报告基因的质粒DNA的表达增加了高达30倍。总之,这些发现表明超声可能有助于提高胶质瘤细胞化疗和基因治疗的疗效。

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