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硅纳米颗粒(SiNPs)对乳腺癌细胞系细胞毒性、氧化应激诱导和细胞凋亡的影响。

The Effect of Silica Nanoparticles (SiNPs) on Cytotoxicity, Induction of Oxidative Stress and Apoptosis in Breast Cancer Cell Lines.

机构信息

Department of Pharmaceutical Biochemistry, Medical University of Bialystok, Mickiewicza 2A, 15-222 Bialystok, Poland.

Division of Chemistry, Biology and Biotechnology, Bialystok University of Technology, Wiejska 45A, 15-351 Bialystok, Poland.

出版信息

Int J Mol Sci. 2023 Jan 20;24(3):2037. doi: 10.3390/ijms24032037.


DOI:10.3390/ijms24032037
PMID:36768363
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9916948/
Abstract

Breast cancer is one of the most common cancers in women. Silica nanoparticles (SiNPs) belong to the group of often-used nanoparticles in biomedical applications. The mechanisms of the cytotoxicity, apoptosis, and oxidative stress induced by the 5-15 nm SiNPs still remain unclear. The aim of the study was to evaluate the anti-cancer effect and mechanism of action of SiNPs in breast cancer cell lines. The breast cancer MDA-MB-231 and ZR-75-1 cell lines were analyzed using MTT assay, flow cytometry, and spectrophotometric methods. In this paper, we presented findings about the cytotoxicity, apoptosis, and oxidative stress in both breast cancer cell lines. We indicated that 5-15 nm SiNPs induced dose-dependent cytotoxicity in MDA-MB-231 and ZR-75-1 cells. Moreover, we demonstrated that the process of apoptosis in the studied cell lines was associated with a decrease in the mitochondrial membrane potential (ΔΨ) and an increase in the activity of caspase-9 and caspase-3. Based on the obtained results, 5-15 nm SiNPs are able to induce the mitochondrial apoptosis pathway. Analyzed nanoparticles have also been found to cause an increase in selected oxidative stress parameters in both breast cancer cell lines. The presented study provides an explanation of the possible mechanisms of 5-15 nm SiNPs action in breast cancer cells.

摘要

乳腺癌是女性最常见的癌症之一。硅纳米颗粒(SiNPs)属于生物医学应用中常用的纳米颗粒之一。目前,其诱导细胞毒性、细胞凋亡和氧化应激的机制仍不清楚。本研究旨在评估 SiNPs 在乳腺癌细胞系中的抗癌作用和作用机制。采用 MTT 检测法、流式细胞术和分光光度法分析乳腺癌 MDA-MB-231 和 ZR-75-1 细胞系。本文介绍了两种乳腺癌细胞系的细胞毒性、细胞凋亡和氧化应激的研究结果。结果表明,5-15nm SiNPs 在 MDA-MB-231 和 ZR-75-1 细胞中诱导了剂量依赖性的细胞毒性。此外,我们证明了研究细胞系中的细胞凋亡过程与线粒体膜电位(ΔΨ)的降低和 caspase-9 和 caspase-3 活性的增加有关。基于获得的结果,5-15nm SiNPs 能够诱导线粒体凋亡途径。分析的纳米颗粒还被发现会导致两种乳腺癌细胞系中选定的氧化应激参数增加。本研究为 5-15nm SiNPs 在乳腺癌细胞中的作用的可能机制提供了一种解释。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1f6/9916948/114442df7c34/ijms-24-02037-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1f6/9916948/8c27d5add43e/ijms-24-02037-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1f6/9916948/949f80c13c30/ijms-24-02037-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1f6/9916948/48b1d05ed6af/ijms-24-02037-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1f6/9916948/9311475292bd/ijms-24-02037-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1f6/9916948/46fa950279fb/ijms-24-02037-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1f6/9916948/114442df7c34/ijms-24-02037-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1f6/9916948/8c27d5add43e/ijms-24-02037-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1f6/9916948/949f80c13c30/ijms-24-02037-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1f6/9916948/48b1d05ed6af/ijms-24-02037-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1f6/9916948/9311475292bd/ijms-24-02037-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1f6/9916948/46fa950279fb/ijms-24-02037-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a1f6/9916948/114442df7c34/ijms-24-02037-g006.jpg

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引用本文的文献

[1]
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本文引用的文献

[1]
The Reduced Graphene Oxide (rGO) Induces Apoptosis, Autophagy and Cell Cycle Arrest in Breast Cancer Cells.

Int J Mol Sci. 2022-8-18

[2]
Silica nanoparticles: Biomedical applications and toxicity.

Biomed Pharmacother. 2022-7

[3]
The Preliminary Study on the Proapoptotic Effect of Reduced Graphene Oxide in Breast Cancer Cell Lines.

Int J Mol Sci. 2021-11-22

[4]
Breast Cancer-Epidemiology, Risk Factors, Classification, Prognostic Markers, and Current Treatment Strategies-An Updated Review.

Cancers (Basel). 2021-8-25

[5]
Nanotechnology and its use in imaging and drug delivery (Review).

Biomed Rep. 2021-5

[6]
Role of oxidative stress in nanoparticles toxicity.

Free Radic Res. 2021-4

[7]
The Size-dependent Cytotoxicity of Amorphous Silica Nanoparticles: A Systematic Review of in vitro Studies.

Int J Nanomedicine. 2020

[8]
Oxidative stress-mediated mitochondrial pathway-dependent apoptosis is induced by silica nanoparticles in cardiomyocytes.

Toxicol Mech Methods. 2020-11

[9]
Apoptosis and oxidative stress as relevant mechanisms of antitumor activity and genotoxicity of ZnO-NPs alone and in combination with N-acetyl cysteine in tumor-bearing mice.

Int J Nanomedicine. 2019-5-27

[10]
Cell death: a review of the major forms of apoptosis, necrosis and autophagy.

Cell Biol Int. 2019-4-25

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