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Nanodiamonds coupled with 5,7-dimethoxycoumarin, a plant bioactive metabolite, interfere with the mitotic process in B16F10 cells altering the actin organization

机译:纳米金刚石与植物生物活性代谢物5,7-二甲氧基香豆素结合,干扰B16F10细胞的有丝分裂过程,从而改变肌动蛋白的组织

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摘要

For the first time, we coupled reduced detonation nanodiamonds (NDs) with a plant secondary metabolite, citropten (5,7-dimethoxycoumarin), and demonstrated how this complex was able to reduce B16F10 tumor cell growth more effectively than treatment with the pure molecule. These results encouraged us to find out the specific mechanism underlying this phenomenon. Internalization kinetics and quantification of citropten in cells after treatment with its pure or ND-conjugated form were measured, and it was revealed that the coupling between NDs and citropten was essential for the biological properties of the complex. We showed that the adduct was not able to induce apoptosis, senescence, or differentiation, but it determined cell cycle arrest, morphological changes, and alteration of mRNA levels of the cytoskeletal-related genes. The identification of metaphasic nuclei and irregular disposition of β-actin in the cell cytoplasm supported the hypothesis that citropten conjugated with NDs showed antimitotic properties in B16F10 cells. This work can be considered a pioneering piece of research that could promote and support the biomedical use of plant drug-functionalized NDs in cancer therapy.
机译:首次,我们将减少爆轰的纳米金刚石(NDs)与植物次生代谢产物柠檬碱(5,7-二甲氧基香豆素)结合使用,并证明了这种复合物如何比纯分子治疗更有效地减少B16F10肿瘤细胞的生长。这些结果鼓励我们找出造成这种现象的具体机制。测定了纯或ND缀合形式处理后的柠檬黄素在细胞中的内在动力学和定量,并且揭示了ND与柠檬酸之间的偶联对于复合物的生物学特性是必不可少的。我们表明,该加合物不能诱导细胞凋亡,衰老或分化,但是它决定了细胞周期停滞,形态变化和细胞骨架相关基因的mRNA水平改变。鉴定细胞相中的核相和β-肌动蛋白的不规则分布,支持了与NDs结合的香柠檬素在B16F10细胞中具有抗有丝分裂特性的假说。这项工作可以被认为是一项开创性研究,可以促进和支持植物药物功能化ND在癌症治疗中的生物医学应用。

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