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肿瘤细胞对巯基丙氨酸修饰金纳米粒子的反应。

Neoplastic cell response to tiopronin-coated gold nanoparticles.

机构信息

Leslie Dan Faculty of Pharmacy, University of Toronto, Toronto, Ontario, Canada.

出版信息

Nanomedicine. 2013 Feb;9(2):264-73. doi: 10.1016/j.nano.2012.05.016. Epub 2012 Jun 9.

Abstract

UNLABELLED

The present study characterized the in vitro biological response of a comprehensive set of cancer cell lines to gold nanoparticles (2.7 nm) coated with tiopronin (AuNPs-TP). Our findings suggest that upon entering cells, the AuNPs-TP are sequestered in vacuoles such as endosomes and lysosomes, and mostly localize in perinuclear areas. Peak cell accumulation was achieved at 8 hours after incubation. L929 and H520 cells showed more than 75% surviving fraction when treated with 0.5 mg/mL of AuNPs-TP for 24 hours, whereas the surviving fractions were 60% in MCF-7 and 20% in HeLa cells. Reactive oxygen species (ROS) production by the AuNPs-TP was dependent on cell line and exposure time. Antioxidants inhibited ROS generation to various extents, with glutathione and tiopronin being most effective. Overall, exposure time, concentration of the AuNPs-TP, and cell line influenced neoplastic cell response. Furthermore, the mechanism of cytotoxicity of the AuNPs-TP was found to be ROS generation.

FROM THE CLINICAL EDITOR

This study describes the basic intracellular characteristics of Tiopronin-Au nanoparticles from the standpoint of their anti-cancer activity in different cancer cell cultures.

摘要

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本研究描述了一系列癌症细胞系对巯基丁二酸包覆的金纳米粒子(AuNPs-TP)的体外生物学反应,提示进入细胞后,AuNPs-TP 被内体和溶酶体等液泡隔离,并主要定位于核周区。孵育 8 小时后细胞摄取达到峰值。当用 0.5mg/mL 的 AuNPs-TP 处理 24 小时时,L929 和 H520 细胞的存活分数超过 75%,而 MCF-7 和 HeLa 细胞的存活分数分别为 60%和 20%。AuNPs-TP 产生的活性氧(ROS)依赖于细胞系和暴露时间。抗氧化剂在不同程度上抑制了 ROS 的产生,其中谷胱甘肽和巯基丁二酸最有效。总之,暴露时间、AuNPs-TP 的浓度和细胞系影响了肿瘤细胞的反应。此外,还发现 Tiopronin-Au 纳米粒子的细胞毒性机制是 ROS 的产生。

临床编辑按

本研究从不同癌症细胞培养物的抗癌活性角度描述了巯基丁二酸-金纳米粒子的基本细胞内特征。

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