Cancer Therapeutic Effects of Titanium Dioxide Nanoparticies Are Associated with Oxidative Stress and Cytokine induction

被引:34
作者
Fujiwara, Rina [1 ]
Luo, Yi [1 ]
Sasaki, Takamitsu [2 ]
Fujii, Kiyonnu [1 ]
Ohmori, Hitoshi [1 ]
Kuniyasu, Hiroki [1 ]
机构
[1] Nara Med Univ, Dept Mol Pathol, Kashihara, Nara 6348521, Japan
[2] Fukuoka Univ, Sch Med, Dept Surg Gastroenterol, Fukuoka 81401, Japan
基金
日本学术振兴会;
关键词
Nanoparticles; Oxidants; Cytokines; APOPTOSIS; OXIDE; GENOTOXICITY; METASTASIS; MECHANISMS; PARTICLES;
D O I
10.1159/000439404
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Nanoparticles (NPs) are considered to influence the inflammatory process; however, the precise mechanism and the significance in tumors are still not clear. In this study, when CT26 and LL2 mouse cancer cells were treated with 6-nm anatase titanium dioxide NPs (TDNPs) without ultraviolet irradiation, oxidative stress and induction of inflammatory cytokines were observed. Oxidative stress was further increased by disease-associated conditions such as high glucose concentrations and hypoxia. Inhaled or orally administered TDNPs generated granulomatous lesions in the lungs and colon of the rodent models tested, with increased oxidative stress and inflammatory cytokines. Oxidative stress and inflammatory cytokines were also found in cancer cells treated with gold or carbon black NPs. Treatment of CT26 cells with 10- to 70-nm rutile TDNPs showed that smaller NPs produced more oxidative stress and inflammatory cytokines than larger ones did. To avoid diffusion of TDNPs and to minimize toxicity, 10-nm TDNPs were suspended in a collagen gel inserted into a subcutaneous tumor in a CT26 mouse. A single TDNP treatment via this method inhibited tumor growth in a size- and dose-dependent manner, and resulted in lower levels of urinary 8-OHdG when compared to systemically administered TDNPs. These findings suggest that TDNPs might be useful for the local treatment of tumors. (C) 2015 S. Karger AG, Basel
引用
收藏
页码:243 / 251
页数:9
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