Accumulation and biological effects of cobalt ferrite nanoparticles in human pancreatic and ovarian cancer cells

被引:49
作者
Pasukoniene, Vita [1 ]
Mlynska, Agata [1 ]
Steponkiene, Simona [2 ]
Poderys, Vilius [2 ]
Matulionyte, Marija [2 ,3 ]
Karabanovas, Vitalijus [2 ]
Statkute, Urte [2 ]
Purviniene, Rasa [1 ]
Krasko, Jan Aleksander [1 ]
Jagminas, Arunas [4 ]
Kurtinaitiene, Marija [4 ]
Strioga, Marius [1 ]
Rotomskis, Ricardas [2 ,3 ]
机构
[1] Natl Canc Inst, Immunol Lab, LT-08660 Vilnius, Lithuania
[2] Natl Canc Inst, Biomed Phys Lab, LT-08660 Vilnius, Lithuania
[3] Vilnius Univ, Laser Res Ctr, Fac Phys, Biophoton Grp, Vilnius, Lithuania
[4] Ctr Phys Sci & Technol, State Res Inst, Lab Nanostruct, Vilnius, Lithuania
来源
MEDICINA-LITHUANIA | 2014年 / 50卷 / 04期
关键词
Superparamagnetic cobalt ferrite nanoparticles; Cytotoxicity; Pancreatic cancer; Ovarian cancer; Cancer stem-like cells; IRON-OXIDE NANOPARTICLES; CONTRAST AGENT; STEM-CELLS; TARGETS; DEXTRAN;
D O I
10.1016/j.medici.2014.09.009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and objective: Superparamagnetic iron oxide nanoparticles (SPIONs) emerge as a promising tool for early cancer diagnostics and targeted therapy. However, both toxicity and biological activity of SPIONs should be evaluated in detail. The aim of this study was to synthesize superparamagnetic cobalt ferrite nanoparticles (Co-SPIONs), and to investigate their uptake, toxicity and effects on cancer stem-like properties in human pancreatic cancer cell line MiaPaCa2 and human ovarian cancer cell line A2780. Materials and methods: Co-SPIONs were produced by Massart's co-precipitation method. The cells were treated with Co-SPIONs at three different concentrations (0.095, 0.48, and 0.95 mu g/mL) for 24 and 48 h. Cell viability and proliferation were analyzed after treatment. The stem-like properties of cells were assessed by investigating the cell clonogenicity and expression of cancer stem cell-associated markers, including CD24/ESA in A2780 cell line and CD44/ALDH1 in MiaPaCa2 cell line. Magnetically activated cell sorting was used for the separation of magnetically labeled and unlabeled cells. Results: Both cancer cell lines accumulated Co-SPIONs, however differences in response to nanoparticles were observed between MiaPaCa2 and A2780 cell. In particular, A2780 cells were more sensitive to exposition to Co-SPIONs than MiaPaCa2 cells, indicating that a safe concentration of nanoparticles must be estimated individually for a particular cell type. Higher doses of Co-SPIONs decreased both the clonogenicity and ESA marker expression in A2780 cells. Conclusions: Co-SPIONs are not cytotoxic to cancer cells, at least when used at a concentration of up to 0.951 mu g/mL. Co-SPIONs have a dose-dependent effect on the clonogenic potential and ESA marker expression in A2780 cells. Magnetic detection of low concentrations of Co-SPIONS in cancer cells is a promising tool for further applications of these nanoparticles in cancer diagnosis and treatment; however, extensive research in this field is needed. (C) 2014 Lithuanian University of Health Sciences. Production and hosting by Elsevier Urban & Partner Sp. z o.o. All rights reserved.
引用
收藏
页码:237 / 244
页数:8
相关论文
共 30 条
[1]   Epigenetic regulation of CD133 and tumorigenicity of CD133+ovarian cancer cells [J].
Baba, T. ;
Convery, P. A. ;
Matsumura, N. ;
Whitaker, R. S. ;
Kondoh, E. ;
Perry, T. ;
Huang, Z. ;
Bentley, R. C. ;
Mori, S. ;
Fujii, S. ;
Marks, J. R. ;
Berchuck, A. ;
Murphy, S. K. .
ONCOGENE, 2009, 28 (02) :209-218
[2]   Superparamagnetic Iron Oxide Nanoparticles Labeling of Bone Marrow Stromal (Mesenchymal) Cells Does Not Affect Their "Stemness'' [J].
Balakumaran, Arun ;
Pawelczyk, Edyta ;
Ren, Jiaqiang ;
Sworder, Brian ;
Chaudhry, Aneeka ;
Sabatino, Marianna ;
Stroncek, David ;
Frank, Joseph A. ;
Robey, Pamela G. .
PLOS ONE, 2010, 5 (07)
[3]   Pancreatic Cancer Stem-like Cells Display Aggressive Behavior Mediated via Activation of FoxQ1 [J].
Bao, Bin ;
Azmi, Asfar S. ;
Aboukameel, Amro ;
Ahmad, Aamir ;
Bolling-Fischer, Aliccia ;
Sethi, Seema ;
Ali, Shadan ;
Li, Yiwei ;
Kong, Dejuan ;
Banerjee, Sanjeev ;
Back, Jessica ;
Sarkar, Fazlul H. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2014, 289 (21) :14520-14533
[4]   Clonogens and cancer stem cells [J].
Baumann, Michael ;
Krause, Mechthild ;
Hill, Richard .
NATURE REVIEWS CANCER, 2008, 8 (12) :990-990
[5]   Dextran and albumin derivatised iron oxide nanoparticles: influence on fibroblasts in vitro [J].
Berry, CC ;
Wells, S ;
Charles, S ;
Curtis, ASG .
BIOMATERIALS, 2003, 24 (25) :4551-4557
[6]   Cell response to dextran-derivatised iron oxide nanoparticles post internalisation [J].
Berry, CC ;
Wells, S ;
Charles, S ;
Aitchison, G ;
Curtis, ASG .
BIOMATERIALS, 2004, 25 (23) :5405-5413
[7]  
Clausell-Tormos J, 2011, ELSE KRONER FRESEN S, V2, P116
[8]   The cancer stem cell: premises, promises and challenges [J].
Clevers, Hans .
NATURE MEDICINE, 2011, 17 (03) :313-319
[9]   Nanoparticle therapeutics: an emerging treatment modality for cancer [J].
Davis, Mark E. ;
Chen, Zhuo ;
Shin, Dong M. .
NATURE REVIEWS DRUG DISCOVERY, 2008, 7 (09) :771-782
[10]   Drug delivery and nanoparticles: Applications and hazards [J].
De Jong, Wim H. ;
Borm, Paul J. A. .
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2008, 3 (02) :133-149