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Flexible ligated ruthenium(II) self-assemblies sensitizes glioma tumor initiating cells in vitro

机译:柔性连接钌(II)自组装在体外敏化神经胶质瘤肿瘤起始细胞

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摘要

The tumorigenic potentials of residual cancer stem-like cells within tumors represent limitations of current cancer therapies. Here, the authors describe the effects of synthesized flexible, ligated, supramolecular self-assembled chair type tetranuclear ruthenium (II) metallacycles (2–5) on glioblastoma and glioma stem like cells. These self-assemblies were observed to be selectively toxic to glioma cells and CD133-positive glioma stem like cells population. Of the self-assembled compounds tested, metallacycle 4 more efficiently induced glioma stem like cells death within a brain cancer cell population and simultaneously inhibited the formation of free-floating gliospheres by reducing the sphere size. Detailed cell death studies revealed that treatment with metallacycle 4 reduced mitochondrial membrane potentials (an indicator of apoptosis) of glioma stem like cells. These results shows the elimination of cancer stem-like cells using an appropriate ligand binding adaptor offers a potential means of developing metal-based compounds for the treatment of chemo-resistant tumors.
机译:肿瘤内残留的癌干样细胞的致瘤潜力代表了当前癌症治疗的局限性。在这里,作者描述了合成的柔性的,结扎的,超分子自组装的椅子型四核钌(II)金属环(2-5)对胶质母细胞瘤和神经胶质瘤干细胞的影响。观察到这些自组装对神经胶质瘤细胞和CD133阳性神经胶质瘤干细胞样细胞群具有选择性毒性。在测试的自组装化合物中,金属环氧化物4更有效地诱导脑癌细胞群内的神经胶质瘤干细胞样细胞死亡,并通过减小球体尺寸来同时抑制自由漂浮的神经胶质球的形成。详细的细胞死亡研究表明,用金属环氧化物4处理可降低胶质瘤干细胞样细胞的线粒体膜电位(凋亡的指标)。这些结果表明,使用合适的配体结合衔接子消除癌症干细胞样细胞,为开发基于金属的化合物治疗化学耐药性肿瘤提供了一种潜在的手段。

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