Effective-by-method for the preparation of folic acid-coated TiO2 nanoparticles with high targeting potential for apoptosis induction against bladder cancer cells (T24)

被引:13
作者
Hanna, Demiana H. H. [1 ]
Aziz, Marina M. M. [1 ]
El Shafee, E. [1 ]
机构
[1] Cairo Univ, Fac Sci, Dept Chem, Giza 12613, Egypt
关键词
apoptosis; cell cycle arrest; cytotoxicity; folic acid-coated TiO2 NPs; ROS; T24 cancer cells; DNA-DAMAGE CHECKPOINT; OXIDE NANOPARTICLES; DOWN-REGULATION; TYROSINE PHOSPHORYLATION; CYCLE ARREST; TUMOR; RADIATION; CDC2; EXPRESSION; PROTEIN;
D O I
10.1002/bab.2456
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The research's goal is to create the surfaces of titanium dioxide nanoparticles (TiO2 NPs) in a layer of folic acid (FA) that can effectively target human bladder cancer cells (T24). An efficient method for creating FA-coated TiO2 NPs was used, and many tools have been used to analyze its physicochemical properties. The cytotoxic effects of FA-coated NPs on T24 cells and the mechanisms of apoptosis generation were examined employing a variety of methodologies. The prepared FA-coated TiO2 NPs suspensions with a hydrodynamic diameter around 37 nm and a negative surface charge of -30 mV reduced T24 cell proliferation with stronger IC50 value (21.8 +/- 1.9 mu g/ml) than TiO2 NPs (47.8 +/- 2.5 mu g/ml). This toxicity resulted in apoptosis induction (16.63%) that was caused through enhanced reactive oxygen species formation and stopping the cell cycle over G2/M phase. Moreover, FA-TiO2 NPs raised the expression levels of P53, P21, BCL2L4, and cleaved Caspase-3, while decreasing Bcl-2, Cyclin B, and CDK1 in treated cells. Overall, these findings revealed efficient targeting of the FA-TiO2 NPs resulted in increasing cellular internalization caused increased apoptosis in T24 cells. As a result, FA-TiO2 NPs might be a viable treatment for human bladder cancer.
引用
收藏
页码:1597 / 1615
页数:19
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