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Genotoxicity Evaluation of Titanium Dioxide Nanoparticles In Vivo and In Vitro: A Meta-Analysis

Journal

TOXICS
Volume 11, Issue 11, Pages -

Publisher

MDPI
DOI: 10.3390/toxics11110882

Keywords

titanium dioxide; nanoparticles; genotoxicity; hazard evaluation; meta-analysis

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This meta-analysis investigates the genotoxicity of titanium dioxide nanoparticles (TiO2 NPs) and explores influencing factors. The results suggest that TiO2 NPs can induce DNA damage, chromosomal damage, and gene mutations, with rats and cancer cells showing higher susceptibility. The DNA damage response mechanism plays a key role in the genotoxicity induced by TiO2 NPs.
Background: Recent studies have raised concerns about genotoxic effects associated with titanium dioxide nanoparticles (TiO2 NPs), which are commonly used. This meta-analysis aims to investigate the potential genotoxicity of TiO2 NPs and explore influencing factors. Methods: This study systematically searched Chinese and English literature. The literature underwent quality evaluation, including reliability evaluation using the toxicological data reliability assessment method and relevance evaluation using routine evaluation forms. Meta-analysis and subgroup analyses were performed using R software, with the standardized mean difference (SMD) as the combined effect value. Results: A total of 26 studies met the inclusion criteria and passed the quality assessment. Meta-analysis results indicated that the SMD for each genotoxic endpoint was greater than 0. This finding implies a significant association between TiO2 NP treatment and DNA damage and chromosome damage both in vivo and in vitro and gene mutation in vitro. Subgroup analysis revealed that short-term exposure to TiO2 NPs increased DNA damage. Rats and cancer cells exhibited heightened susceptibility to DNA damage triggered by TiO2 NPs (p < 0.05). Conclusions: TiO2 NPs could induce genotoxicity, including DNA damage, chromosomal damage, and in vitro gene mutations. The mechanism of DNA damage response plays a key role in the genotoxicity induced by TiO2 NPs.

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