首页> 美国卫生研究院文献>Molecular Cancer >FL118 a novel camptothecin derivative is insensitive to ABCG2 expression and shows improved efficacy in comparison with irinotecan in colon and lung cancer models with ABCG2-induced resistance
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FL118 a novel camptothecin derivative is insensitive to ABCG2 expression and shows improved efficacy in comparison with irinotecan in colon and lung cancer models with ABCG2-induced resistance

机译:FL118是一种新型喜树碱衍生物对ABCG2表达不敏感与伊立替康相比在具有ABCG2诱导耐药性的结肠癌和肺癌模型中显示出比伊立替康更高的疗效

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摘要

BackgroundIrinotecan is a camptothecin analogue currently used in clinical practice to treat advanced colorectal cancer. However, acquired resistance mediated by the drug efflux pump ABCG2 is a recognized problem. We reported on a novel camptothecin analogue, FL118, which shows anticancer activity superior to irinotecan. In this study, we sought to investigate the potency of FL118 versus irinotecan or its active metabolite, SN-38, in both in vitro and in vivo models of human cancer with high ABCG2 activity. We also sought to assess the potency and ABCG2 affinity of several FL118 analogues with B-ring substitutions.
机译:背景技术伊立替康是目前在临床实践中用于治疗晚期结直肠癌的喜树碱类似物。然而,由药物外排泵ABCG2介导的获得性耐药是公认的问题。我们报道了一种新型喜树碱类似物FL118,其抗癌活性优于伊立替康。在这项研究中,我们试图研究在具有高ABCG2活性的人类癌症的体外和体内模型中,FL118与伊立替康或其活性代谢产物SN-38的效力。我们还试图评估几种具有B环取代的FL118类似物的效价和ABCG2亲和力。

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