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金属纳米颗粒在体外乳腺癌模型中的抗增殖活性

Anti-proliferative Activities of Metallic Nanoparticles in an in Vitro Breast Cancer Model.

作者信息

Loutfy Samah A, Al-Ansary Nadia A, Abdel-Ghani Nour T, Hamed Ahmed R, Mohamed Mona B, Craik James D, Eldin Taher A Salah, Abdellah Ahmed M, Hussein Yassmein, Hasanin M T M, Elbehairi Serag Eldin I

机构信息

Virology and Immunology Unit, Cancer Biology Department, National Cancer Institute, Cairo University, Cairo, Egypt E-mail :

出版信息

Asian Pac J Cancer Prev. 2015;16(14):6039-46. doi: 10.7314/apjcp.2015.16.14.6039.

Abstract

AIMS

To investigate effect of metallic nanoparticles, silver (AgNPs) and gold nanoparticles (AuNPs) as antitumor treatment in vitro against human breast cancer cells (MCF-7) and their associated mechanisms. This could provide new class of engineered nanoparticles with desired physicochemical properties and may present newer approaches for therapeutic modalities to breast cancer in women.

MATERIALS AND METHODS

A human breast cancer cell line (MCF-7) was used as a model of cells. Metallic nanoparticles were characterized using UV-visible spectra and transmission electron microscopy (TEM). Cytotoxic effects of metallic nanoparticles on MCF-7 cells were followed by colorimetric SRB cell viability assays, microscopy, and cellular uptake. Nature of cell death was further investigated by DNA analysis and flow cytometry.

RESULTS

Treatment of MCF-7 with different concentrations of 5-10nm diameter of AgNPs inhibited cell viability in a dose-dependent manner, with IC50 value of 6.28μM, whereas treatment of MCF-7 with different concentrations of 13-15nm diameter of AuNPs inhibited cell viability in a dose-dependent manner, with IC50 value of 14.48μM. Treatment of cells with a IC50 concentration of AgNPs generated progressive accumulation of cells in the S phase of the cell cycle and prevented entry into the M phase. The treatment of cells with IC50 concentrations of AuNPs similarly generated progressive accumulation of cells in sub-G1 and S phase, and inhibited the entrance of cells into the M phase of the cell cycle. DNA fragmentation, as demonstrated by electrophoresis, indicated induction of apoptosis.

CONCLUSIONS

Our engineered silver nanoparticles effectively inhibit the proliferation of human breast carcinoma cell line MCF-7 in vitro at high concentration (1000 μM) through apoptotic mechanisms, and may be a beneficial agent against human carcinoma but further detailed study is still needed.

摘要

目的

研究金属纳米颗粒,即银纳米颗粒(AgNPs)和金纳米颗粒(AuNPs)作为体外抗肿瘤治疗对人乳腺癌细胞(MCF-7)的作用及其相关机制。这可为具有所需物理化学性质的新型工程纳米颗粒提供依据,并可能为女性乳腺癌的治疗方式提供新方法。

材料与方法

使用人乳腺癌细胞系(MCF-7)作为细胞模型。通过紫外可见光谱和透射电子显微镜(TEM)对金属纳米颗粒进行表征。采用比色法SRB细胞活力测定、显微镜观察和细胞摄取来跟踪金属纳米颗粒对MCF-7细胞的细胞毒性作用。通过DNA分析和流式细胞术进一步研究细胞死亡的性质。

结果

用不同浓度直径为5-10nm的AgNPs处理MCF-7细胞,以剂量依赖性方式抑制细胞活力,IC50值为6.28μM;而用不同浓度直径为13-15nm的AuNPs处理MCF-7细胞,以剂量依赖性方式抑制细胞活力,IC50值为14.48μM。用IC50浓度的AgNPs处理细胞会导致细胞在细胞周期的S期逐渐积累,并阻止其进入M期。用IC50浓度的AuNPs处理细胞同样会使细胞在亚G1期和S期逐渐积累,并抑制细胞进入细胞周期的M期。电泳显示的DNA片段化表明诱导了细胞凋亡。

结论

我们制备的银纳米颗粒在高浓度(1000μM)下通过凋亡机制有效抑制人乳腺癌细胞系MCF-7的体外增殖,可能是一种抗人癌的有益药物,但仍需进一步详细研究。

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