Asian Pacific Journal of Cancer Prevention

  • 제16권14호
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  • Pages.6039-6046
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  • 2015
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  • 1513-7368(pISSN)
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  • 2476-762X(eISSN)
아시아태평양암예방학회 (Asian Pacific Journal of Cancer Prevention)
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Anti-proliferative Activities of Metallic Nanoparticles in an in Vitro Breast Cancer Model

  • Loutfy, Samah A (Virology and Immunology Unit, Cancer Biology Department, National Cancer Institute) ;
  • Al-Ansary, Nadia A (Photochemistry & Photobiology, LAMPA, National Institute of Laser Enhanced Sciences) ;
  • Abdel-Ghani, Nour T (Chemistry Department, Faculty of Science, Cairo University) ;
  • Hamed, Ahmed R (Phytochemistry Department and Center of Excellence for Advanced Sciences, National Research Centre) ;
  • Mohamed, Mona B (Photochemistry & Photobiology, LAMPA, National Institute of Laser Enhanced Sciences) ;
  • Craik, James D (Biochemistry Department, Faculty of Medicine, Health Sciences Center, Kuwait University) ;
  • Eldin, Taher A. Salah (Director of Nanotechnology Characterization Center, Agricultural Research Center) ;
  • Abdellah, Ahmed M (Photochemistry & Photobiology, LAMPA, National Institute of Laser Enhanced Sciences) ;
  • Hussein, Yassmein (Nanotech) ;
  • Hasanin, MTM (Nanotech) ;
  • Elbehairi, Serag Eldin I (Egyptian Organization for Biological Products and Vaccines)
  • 발행 : 2015.09.02
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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 $6.28{\mu}M$, 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 $14.48{\mu}M$. 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 ($1000{\mu}M$) through apoptotic mechanisms, and may be a beneficial agent against human carcinoma but further detailed study is still needed.

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