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
Virology and Immunology Unit, Cancer Biology Department, National Cancer Institute, Cairo University, Cairo, Egypt E-mail :
Asian Pac J Cancer Prev. 2015;16(14):6039-46. doi: 10.7314/apjcp.2015.16.14.6039.
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.
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.
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.
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.
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。
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。
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。
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。