体外小尺寸银纳米粒子抑制神经胶质细胞瘤细胞中基于 sonic hedgehog 通路的增殖。

Suppression of sonic hedgehog pathway-based proliferation in glioblastoma cells by small-size silver nanoparticles in vitro.

机构信息

Department of Biotechnology and Cell Biology, Medical College, University of Information Technology and Management in Rzeszow, St. Sucharskiego 2, 35-225, Rzeszow, Poland.

Medical Biotechnology Student's Science Group "Helisa", Medical College, University of Information Technology and Management, St. Sucharskiego 2, 35-225, Rzeszow, Poland.

出版信息

Arch Toxicol. 2023 Sep;97(9):2385-2398. doi: 10.1007/s00204-023-03552-x. Epub 2023 Jul 5.

Abstract

Glioblastomas (GBs) are one of the most aggressive and invasive intracranial cancers. Recently, it has been postulated that, among other factors, the hedgehog (HH) pathway may be a key factor in this phenomenon. Moreover, it has been reported that small-size silver nanoparticles (AgNPs) are characterized by a high cytotoxic effect towards GBs. However, their effect on the sonic hedgehog (SHH) pathway has never been demonstrated in any cancer cells. Therefore, the aim of the present study was to evaluate the impact of the anti-proliferative properties of 5-nm AgNPs on the SHH pathway in the GB cell line (U-87MG) in vitro. The results showed a time- and dose-dependent decrease in the metabolic activity in the U-87MG cells treated with AgNPs, with IC reaching 30.41 and 21.16 µg/mL after 24 h and 48 h, respectively, followed by an increase in the intracellular reactive oxygen species (ROS) level. The co-treatment of the cells with AgNPs and Robotnikinin (SHH inhibitor) abolished and/or strengthened the effect of AgNPs, especially on the SHH mRNA levels and on the PCNA, PTCH1, Gli1, and SUFU protein levels. Interestingly, no changes in the level of ERK1/2, Akt, and SRC kinase protein expression were detected, suggesting a direct impact of AgNPs and/or ROS on the inhibition of the canonical SHH pathway. However, more studies are needed due to the increase in the mTOR protein expression after the treatment of the cells with AgNPs, as in the Robotnikinin treatment. In conclusion, small-size AgNPs are able to inhibit the proliferation of GB cells in vitro by suppressing the canonical SHH pathway.

摘要

胶质母细胞瘤(GBs)是颅内最具侵袭性和侵略性的癌症之一。最近,有人假设,除其他因素外,刺猬(HH)途径可能是这种现象的关键因素。此外,据报道,小尺寸的银纳米粒子(AgNPs)对 GB 具有高细胞毒性作用。然而,它们对任何癌细胞中的 sonic 刺猬(SHH)途径的影响从未在任何癌细胞中得到证明。因此,本研究旨在评估 5nm AgNPs 的抗增殖特性对体外 GB 细胞系(U-87MG)中 SHH 途径的影响。结果显示,AgNPs 处理的 U-87MG 细胞的代谢活性呈时间和剂量依赖性下降,IC 在 24 小时和 48 小时后分别达到 30.41 和 21.16μg/mL,随后细胞内活性氧(ROS)水平升高。用 AgNPs 和 Robotnikinin(SHH 抑制剂)共同处理细胞可消除和/或增强 AgNPs 的作用,尤其是对 SHH mRNA 水平以及 PCNA、PTCH1、Gli1 和 SUFU 蛋白水平的作用。有趣的是,未检测到 ERK1/2、Akt 和 SRC 激酶蛋白表达水平的变化,这表明 AgNPs 和/或 ROS 直接影响经典 SHH 途径的抑制。然而,由于在用 AgNPs 处理细胞后 mTOR 蛋白表达增加,需要进行更多的研究,就像在用 Robotnikinin 处理时一样。总之,小尺寸的 AgNPs 能够通过抑制经典的 SHH 途径抑制体外 GB 细胞的增殖。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2297/10404180/53fa03dc8012/204_2023_3552_Fig1_HTML.jpg

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