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Shining light on nuclear-targeted therapy using gold nanostar constructs

机译:使用金纳米星构建体为核靶向治疗提供光辉

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摘要

Nuclear-targeted therapy has received increasing attention as a potential strategy to improve the therapeutic efficacy of treating cancer. The main agents to the cancer cell nucleus. Nanoparticles as nanocarriers have started to address some of these issues. However, a lack of understanding in how nanoconstructs interact with the nucleus has precluded detailed studies. In this article, we highlight a nanoconstruct composed of gold (Au) nanostars loaded with nucleolin-specific aptamers. This nanoconstruct induced major changes in the nuclear phenotype through nuclear envelope (NE) invaginations. Femtosecond, light-triggered release of the aptamers from the surface of the Au nanostars further increased the number of NE deformations. Cancer cells with more NE folding showed increased apoptosis as well as decreased cell viability. The author’s of this article have revealed that correlation between drug-induced changes in nuclear phenotypes and increased therapeutic efficacy can provide new insight into nuclear-targeted cancer therapy.
机译:靶向核疗法作为一种提高治疗癌症疗效的潜在策略受到越来越多的关注。主要作用于癌细胞核。作为纳米载体的纳米颗粒已经开始解决其中一些问题。但是,由于缺乏对纳米结构与细胞核相互作用的了解,因此无法进行详细的研究。在本文中,我们重点介绍了由金(Au)纳米星组成的纳米结构,其中载有核仁蛋白特异性适体。这种纳米结构通过核包膜(NE)内陷诱导了核表型的重大变化。飞秒的光触发从金纳米星的表面释放适体,进一步增加了NE变形的数量。 NE折叠更多的癌细胞显示出增加的细胞凋亡以及降低的细胞活力。本文的作者透露,药物诱导的核表型变化与治疗效果增强之间的相关性可以为以核靶向的癌症治疗提供新的见识。

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