核仁素
适体
癌细胞
核心
生物物理学
胶体金
细胞核
细胞
纳米技术
化学
细胞生物学
癌症研究
癌症
材料科学
纳米颗粒
生物化学
生物
分子生物学
遗传学
核仁
作者
Duncan Hieu M. Dam,Jung Heon Lee,Patrick N. Sisco,Dick T. Co,Ming Zhang,Michael R. Wasielewski,Teri W. Odom
出处
期刊:ACS Nano
[American Chemical Society]
日期:2012-03-22
卷期号:6 (4): 3318-3326
被引量:256
摘要
We report the direct visualization of interactions between drug-loaded nanoparticles and the cancer cell nucleus. Nanoconstructs composed of nucleolin-specific aptamers and gold nanostars were actively transported to the nucleus and induced major changes to the nuclear phenotype via nuclear envelope invaginations near the site of the construct. The number of local deformations could be increased by ultrafast, light-triggered release of the aptamers from the surface of the gold nanostars. Cancer cells with more nuclear envelope folding showed increased caspase 3 and 7 activity (apoptosis) as well as decreased cell viability. This newly revealed correlation between drug-induced changes in nuclear phenotype and increased therapeutic efficacy could provide new insight for nuclear-targeted cancer therapy.
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