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Effect of Titanium Dioxide Nanoparticles on Mammalian Cell Cycle In Vitro: A Systematic Review and Meta-Analysis
被引:14
作者:
Chang, Hongmei
[1
]
Wang, Qianqian
[1
]
Meng, Xiaojia
[1
]
Chen, Xinyu
[2
]
Deng, Yaxin
[1
]
Li, Li
[1
]
Yang, Yaqian
[1
]
Song, Guanling
[1
]
Jia, Huaimiao
[3
]
机构:
[1] Shihezi Univ, Sch Med, Dept Prevent Med, Key Labs Xinjiang Endem & Ethn Dis, Shihezi 832003, Peoples R China
[2] Nanjing Med Univ, Sch Publ Hlth, Dept Epidemiol & Biostat, Nanjing 210019, Peoples R China
[3] Shihezi Ctr Dis Control & Prevent, Dept Endem Dis, Shihezi 832003, Xinjiang, Peoples R China
基金:
中国国家自然科学基金;
关键词:
DNA-DAMAGE RESPONSE;
DOUBLE-STRAND BREAKS;
TIO2;
NANOPARTICLES;
OXIDATIVE STRESS;
CYTOTOXICITY;
ARREST;
CANCER;
APOPTOSIS;
PATHWAY;
GENOTOXICITY;
D O I:
10.1021/acs.chemrestox.1c00402
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
Although most studies that explore the cytotoxicity of titanium dioxide nanoparticles (nano-TiO2) have focused on cell viability and oxidative stress, the cell cycle, a basic process of cell life, can also be affected. However, the results on the effects of nanoTiO(2) on mammalian cell cycle are still inconsistent. A systematic review and meta-analysis were therefore performed in this research based on the effects of nano-TiO2 on the mammalian cell cycle in vitro to explore whether nano-TiO(2 )can induce cell cycle arrest. Meanwhile, the impact of physicochemical properties of nano-TiO(2 )on the cell cycle in vitro was investigated, and the response of normal cells and cancer cells was compared. A total of 33 articles met the eligibility criteria after screening. We used Review Manager 5.4 and Stata 15.1 for analysis. The results showed an increased percentage of cells in the sub-GI phase and an upregulation of the p53 gene after being exposed to nano-TiO2. Nevertheless, nano-TiO(2 )had no effect on cell percentage in other phases of the cell cycle. Furthermore, subgroup analysis revealed that the cell percentage in both the sub-G1 phase of normal cells and S phase of cancer cells were significantly increased under anatase-form nano-TiO(2 )treatment. Moreover, nano-TiO(2 )with a particle size <25 nm or exposure duration of nano-TiO(2 )more than 24 h induced an increased percentage of normal cells in the sub-G1 phase. In addition, the cell cycle of cancer cells was arrested in the S phase no matter if the exposure duration of nano-TiO(2 )was more than 24 h or the exposure concentration was over 50 mu g/mL. In conclusion, this study demonstrated that nano-TiO(2 )disrupted the cell cycle in vitro. The cell cycle arrest induced by nano-TiO(2 )varies with cell status and physicochemical properties of nano-TiO2.
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页码:1435 / 1456
页数:22
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