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Targeting ferritin receptors for the selective delivery of imaging and therapeutic agents to breast cancer cells

机译:针对铁蛋白受体的选择性成像和治疗制剂乳腺癌细胞

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In this work the selective uptake of native horse spleen ferritin and apoferritin loaded with MRI contrast agents has been assessed in human breast cancer cells (MCF-7 and MDA-MB-231). The higher expression of L-ferritin receptors (SCARA5) led to an enhanced uptake in MCF-7 as shown in T-2 and T-1 weighted MR images, respectively. The high efficiency of ferritin internalization in MCF-7 has been exploited for the simultaneous delivery of curcumin, a natural therapeutic molecule endowed with antineoplastic and anti-inflammatory action, and the MRI contrast agent Gd-HPDO3A. This theranostic system is able to treat selectively breast cancer cells over-expressing ferritin receptors. By entrapping in apoferritin both Gd-HPDO3A and curcumin, it was possible to deliver a therapeutic dose of 167 mu g ml(-1) (as calculated by MRI) of this natural drug to MCF-7 cells, thus obtaining a significant reduction of cell proliferation.
机译:在这工作的选择性吸收本地马脾脏铁蛋白和去铁铁蛋白含有核磁共振在人类乳腺癌造影剂被评估癌细胞(MCF-7和mda - mb - 231)。L-ferritin受体的表达(SCARA5)领导一个增强的吸收在MCF-7如2所示分别和t - 1先生加权图像。效率高的铁蛋白内化同时MCF-7被剥削姜黄素,一种天然的治疗分子具有抗肿瘤药抗炎作用,核磁共振对比代理Gd-HPDO3A。治疗乳腺癌细胞选择性过度表达铁蛋白受体。在去铁铁蛋白Gd-HPDO3A和姜黄素,它可以提供治疗剂量的167μg毫升(1)(MRI)计算天然药物MCF-7细胞,从而获得细胞增殖显著减少。

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