The Effects of the Food Additive Titanium Dioxide (E171) on Tumor Formation and Gene Expression in the Colon of a Transgenic Mouse Model for Colorectal Cancer

被引:10
|
作者
Bischoff, Nicolaj S. [1 ]
Proquin, Heloise [1 ,2 ]
Jetten, Marlon J. [1 ,3 ]
Schrooders, Yannick [1 ]
Jonkhout, Marloes C. M. [1 ,4 ]
Briede, Jacco J. [1 ]
van Breda, Simone G. [1 ]
Jennen, Danyel G. J. [1 ]
Medina-Reyes, Estefany, I [5 ]
Delgado-Buenrostro, Norma L. [5 ]
Chirino, Yolanda, I [5 ]
van Loveren, Henk [1 ]
de Kok, Theo M. [1 ]
机构
[1] Maastricht Univ, GROW Sch Oncol & Reprod, Dept Toxicogen, Med Ctr, NL-6229 ER Maastricht, Netherlands
[2] Natl Inst Publ Hlth & Environm RIVM, NL-3721 MA De Bilt, Netherlands
[3] Maastricht Univ, Fac Hlth Med & Life Sci, Med Ctr, NL-6229 ES Maastricht, Netherlands
[4] Katholieke Univ Leuven, Lab Biosignaling & Therapeut, Dept Cellular & Mol Med, B-3000 Leuven, Belgium
[5] Univ Nacl Autonoma Mexico, Fac Estudios Super Iztacala, Lab Carcinogenesis & Toxicol, Unidad Biomed, Mexico City 54090, DF, Mexico
关键词
titanium dioxide; E171; mice; transgenic; tumor formation; gene expression; toxicology; in vivo; INFLAMMATION; RHYTHMS;
D O I
10.3390/nano12081256
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Titanium dioxide (TiO2) is present in many different food products as the food additive E171, which is currently scrutinized due to its potential adverse effects, including the stimulation of tumor formation in the gastrointestinal tract. We developed a transgenic mouse model to examine the effects of E171 on colorectal cancer (CRC), using the Cre-LoxP system to create an Apc-gene-knockout model which spontaneously develops colorectal tumors. A pilot study showed that E171 exposed mice developed colorectal adenocarcinomas, which were accompanied by enhanced hyperplasia in epithelial cells, and increased tumor size. In the main study, tumor formation was studied following the exposure to 5 mg/kg(bw)/day of E171 for 9 weeks (Phase I). E171 exposure showed a statistically nonsignificant increase in the number of colorectal tumors in these transgenic mice, as well as a statistically nonsignificant increase in the average number of mice with tumors. Gene expression changes in the colon were analyzed after exposure to 1, 2, and 5 mg/kg(bw)/day of E171 for 2, 7, 14, and 21 days (Phase II). Whole-genome mRNA analysis revealed the modulation of genes in pathways involved in the regulation of gene expression, cell cycle, post-translational modification, nuclear receptor signaling, and circadian rhythm. The processes associated with these genes might be involved in the enhanced tumor formation and suggest that E171 may contribute to tumor formation and progression by modulation of events related to inflammation, activation of immune responses, cell cycle, and cancer signaling.
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页数:28
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