Antitumor activity of photo-stimulated zinc oxide nanoparticles combined with paclitaxel or cisplatin in HNSCC cell lines

被引:60
作者
Hackenberg, Stephan [1 ]
Scherzed, Agmal [1 ]
Harnisch, Wilma [1 ]
Froelich, Katrin [1 ]
Ginzkey, Christian [1 ]
Koehler, Christian [1 ]
Hagen, Rudolf [1 ]
Kleinsasser, Norbert [1 ]
机构
[1] Univ Wurzburg, Dept Otorhinolaryngol Plast Aesthet & Reconstruct, D-97080 Wurzburg, Germany
关键词
Nanoparticle; Zinc oxide; UV irradiation; Photocatalytic; HNSCC; IN-VITRO; INDUCTION CHEMOTHERAPY; TIO2; NANOPARTICLES; ZNO NANOPARTICLES; CARCINOMA; PARTICLES; CANCER; HEAD; NECK; TOXICITY;
D O I
10.1016/j.jphotobiol.2012.05.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Zinc oxide nanoparticles (ZnO-NPs) exhibit photocatalytic properties and are used in sunscreen cosmetics and for the degradation of environmental pollutants. Furthermore, ZnO-NPs have proven to induce tumor-selective cell death in human squamous cell carcinoma (HNSCC) in vitro. The aim of the current study was to evaluate cytotoxic effects of UVA-1-activated ZnO-NPs in combination with paclitaxel and cisplatin in HNSCC. Three HNSCC cell lines (HLaC-78, Cal-27 and PJ-41) were incubated with ZnO-NPs at concentrations of 0.02 and 0.2 mu g/ml in combination with paclitaxel (0.5-5 nM) or cisplatin (0.03-3 mu M) for 24 h. Afterwards, cells were irradiated with UVA-1 for 15 min. Viability was measured by MTT assay, fluorescein-diacetate (FDA) test and annexin/propidiumiodide flow cytometry. A significant decrease in viable cells could be observed in all three HNSCC cell lines treated by photocatalytic therapy with 0.2 mu g/cm(2) ZnO-NPs alone. A combination with paclitaxel or cisplatin at low concentrations resulted in a further increase in cytotoxicity in vitro revealing a synergistic effect. Flow cytometry revealed a combination of apoptosis and necrosis. These results indicate that photocatalytic therapy of HNSCC with ZnO-NPs could enhance the cytotoxic action of chemotherapeutic agents synergistically, indicating a promising potential for ZnO-NPs in antitumor applications. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:87 / 93
页数:7
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