Glucose capped silver nanoparticles induce cell cycle arrest in HeLa cells

被引:54
作者
Panzarini, Elisa [1 ]
Mariano, Stefania [1 ]
Vergallo, Cristian [1 ]
Carata, Elisabetta [1 ]
Fimia, Gian Maria [1 ]
Mura, Francesco [2 ]
Rossi, Marco [2 ]
Vergaro, Viviana [1 ]
Ciccarella, Giuseppe [1 ,5 ]
Corazzari, Marco [4 ]
Dini, Luciana [1 ,3 ]
机构
[1] Univ Salento, Dept Biol & Environm Sci & Technol DiSTeBA, Lecce, Italy
[2] Sapienza Univ Rome, Dept Base & Appl Sci Engn, Rome, Italy
[3] CNR Nanotec, Lecce, Italy
[4] Univ Roma Tor Vergata, Dept Biol, Rome, Italy
[5] CNR, CNR NANOTEC, Inst Nanotechnol, Via Monteroni, I-73100 Lecce, Italy
关键词
Silver nanoparticles (AgNPs); Cytotoxicity; Cell cycle; Nanoparticles uptake; HeLa cells; SURFACE-CHEMISTRY; NANO-SILVER; DNA-DAMAGE; TOXICITY; CYTOTOXICITY; GLYCONANOPARTICLES; APOPTOSIS; GOLD; ACTIVATION; EXPRESSION;
D O I
10.1016/j.tiv.2017.02.014
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
This study aims to determine the interaction (uptake and biological effects on cell viability and cell cycle progression) of glucose capped silver nanoparticles (AgNPs-G) on human epithelioid cervix carcinoma (HeLa) cells, in relation to amount, 2 x 10(3) or 2 x 10(4) NPs/cell, and exposure time, up to 48 h. The spherical and well dispersed AgNPs (30 5 nm) were obtained by using glucose as reducing agent in a green synthesis method that ensures to stabilize AgNPs avoiding cytotoxic soluble silver ions Ag+ release. HeLa cells take up abundantly and rapidly AgNPs-G resulting toxic to cells in amount and incubation time dependent manner. HeLa cells were arrested at S and G2/M phases of the cell cycle and subG1 population increased when incubated with 2 x 10(4) AgNPs-G/cell. Mitotic index decreased accordingly. The dissolution experiments demonstrated that the observed effects were due only to AgNPs-G since glucose capping prevents Ag+ release. The AgNPs-G influence on HeLa cells viability and cell cycle progression suggest that AgNPs-G, alone or in combination with chemotherapeutics, may be exploited for the development of novel antiproliferative treatment in cancer therapy. However, the possible influence of the cell cycle on cellular uptake of AgNPs-G and the mechanism of AgNPs entry in cells need further investigation. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:64 / 74
页数:11
相关论文
共 47 条
[1]   DNA damage response to different surface chemistry of silver nanoparticles in mammalian cells [J].
Ahamed, Maqusood ;
Karns, Michael ;
Goodson, Michael ;
Rowe, John ;
Hussain, Saber M. ;
Schlager, John J. ;
Hong, Yiling .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2008, 233 (03) :404-410
[2]  
Albanese A, 2012, ANNU REV BIOMED ENG, V14, P1, DOI [10.1146/annurev-bioeng-071811-150124, 10.1146/annurev.bioeng-071811-150124]
[3]  
[Anonymous], 2011, W WILSON DATABASE
[4]   Cellular responses induced by silver nanoparticles:: In vitro studies [J].
Arora, S. ;
Jain, J. ;
Rajwade, J. M. ;
Paknikar, K. M. .
TOXICOLOGY LETTERS, 2008, 179 (02) :93-100
[5]   Anti-proliferative activity of silver nanoparticles [J].
AshaRani, P. V. ;
Hande, M. Prakash ;
Valiyaveettil, Suresh .
BMC CELL BIOLOGY, 2009, 10 :65
[6]  
Asharani Pv, 2012, Genome Integr, V3, P2, DOI 10.1186/2041-9414-3-2
[7]   Silver Nanoparticles Biosynthesized Using Achillea biebersteinii Flower Extract: Apoptosis Induction in MCF-7 Cells via Caspase Activation and Regulation of Bax and Bcl-2 Gene Expression [J].
Baharara, Javad ;
Namvar, Farideh ;
Ramezani, Tayebe ;
Mousavi, Marzieh ;
Mohamad, Rosfarizan .
MOLECULES, 2015, 20 (02) :2693-2706
[8]   The influence of Citrate or PEG coating on silver nanoparticle toxicity to a human keratinocyte cell line [J].
Bastos, V. ;
Ferreira de Oliveira, J. M. P. ;
Brown, D. ;
Jonhston, H. ;
Malheiro, E. ;
Daniel-da-Silva, A. L. ;
Duarte, I. F. ;
Santos, C. ;
Oliveira, H. .
TOXICOLOGY LETTERS, 2016, 249 :29-41
[9]   Toxicity of silver nanoparticles-Nanoparticle or silver ion? [J].
Beer, Christiane ;
Foldbjerg, Rasmus ;
Hayashi, Yuya ;
Sutherland, Duncan S. ;
Autrup, Herman .
TOXICOLOGY LETTERS, 2012, 208 (03) :286-292
[10]   Silver nanoparticles induce toxicity in A549 cells via ROS-dependent and ROS-independent pathways [J].
Chairuangkitti, Porntipa ;
Lawanprasert, Somsong ;
Roytrakul, Sittiruk ;
Aueviriyavit, Sasitorn ;
Phummiratch, Duangkamol ;
Kulthong, Kornphimol ;
Chanvorachote, Pithi ;
Maniratanachote, Rawiwan .
TOXICOLOGY IN VITRO, 2013, 27 (01) :330-338