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Photodynamic therapy enhances the efficacy of gene-directed enzyme prodrug therapy

机译:光动力疗法增强了基因导向酶前药疗法的功效

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摘要

IntroductionGene-directed enzyme prodrug therapy (GDEPT) employing the cytosine deaminase (CD) gene, which encodes an enzyme that converts the nontoxic agent 5-fluorocytosine (5-FC) into the chemotherapeutic drug 5-fluorouracil (5-FU), has shown promise both in experimental animals and in clinical trials. Nevertheless, with the transfection systems available presently the percentage of tumor cells incorporating the desired gene is usually too low for successful therapy. We have examined the ability of photodynamic therapy (PDT) to enhance the efficacy of the metabolites, converted from 5-FC by CD gene transfected rat glioma cells.
机译:简介采用胞嘧啶脱氨酶(CD)基因的基因导向酶前药疗法(GDEPT),该基因编码将无毒药物5-氟胞嘧啶(5-FC)转换为化学治疗药物5-氟尿嘧啶(5-FU)的酶。在实验动物和临床试验中都有希望。然而,利用目前可用的转染系统,掺入所需基因的肿瘤细胞的百分比通常太低而无法成功治疗。我们已经研究了光动力疗法(PDT)增强由CD基因转染的大鼠神经胶质瘤细胞从5-FC转换而来的代谢物功效的能力。

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