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Gene therapy for hepatocellular carcinoma using sonoporation enhanced by contrast agents

机译:造影剂增强声波穿孔治疗肝细胞癌的基因治疗

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摘要

We examined whether sonoporation enhanced by a contrast agent (BR14) was effective in gene therapy for hepatocelluar carcinoma (HCC). Human hepatic cancer cells (SK-Hep1) and plasmid cDNAs expressing green fluorescent protein (GFP), interferon (IFN), and LacZ were used. In vitro, SK-Hep1 cell suspensions with DNA and BR14 were sonoporated. Expressions of every plasmid cDNA and the antitumor effect of IFN were analyzed. In vivo, GFP and IFN genes with BR14 were directly injected into subcutaneous tumors using SK-Hep1 in nude mice, and transcutaneous sonoporation of the tumors was performed. GFP gene transfections and tumor diameters after IFN gene transfection were examined. In vitro, no SK-Hep1 cells were transfected without sonication, whereas transfections were successful after sonication with BR14. Antitumor effect of IFN gene transfection by ultrasound (US) and with BR14 was revealed. In vivo, the SK-Hep1 cells expressed GFP, and the IFN gene transfection by US with BR14 reduced tumor size significantly. In conclusion, gene therapy with sonoporation enhanced by a contrast agent may become a new treatment option for HCC.
机译:我们检查了造影剂(BR14)增强的声纳穿孔在肝细胞癌(HCC)的基因治疗中是否有效。使用人肝癌细胞(SK-Hep1)和表达绿色荧光蛋白(GFP),干扰素(IFN)和LacZ的质粒cDNA。在体外,将具有DNA和BR14的SK-Hep1细胞悬液进行声穿孔。分析了每种质粒cDNA的表达和IFN的抗肿瘤作用。在体内,使用SK-Hep1将具有BR14的GFP和IFN基因直接注射到皮下肿瘤中,并经皮超声处理肿瘤。检查GFP基因转染和IFN基因转染后的肿瘤直径。在体外,未经超声处理,没有SK-Hep1细胞被转染,而BR14进行超声处理后,转染成功。揭示了超声(US)和BR14转染IFN基因的抗肿瘤作用。在体内,SK-Hep1细胞表达GFP,而US用BR14转染IFN基因可显着降低肿瘤大小。总之,用造影剂增强声波穿孔的基因治疗可能成为肝癌的新治疗选择。

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