Related Experiment Video
Updated: May 8, 2025

10:26
Photopatterning Proteins and Cells in Aqueous Environment Using TiO2 Photocatalysis
Published on: October 26, 2015
7.8K
Exposure to a Titanium Dioxide Product Alters DNA Methylation in Human Cells
Carlos Wells1, Marta Pogribna1, Arjun Sharmah2
1Division of Biochemical Toxicity, FDA/National Center for Toxicological Research, Jefferson, AR 72079, USA.
Nanomaterials (Basel, Switzerland)
|December 27, 2024
Summary
Titanium dioxide (TiO2) exposure impacts DNA methylation in human cells, affecting global methylation and specific gene promoters. This epigenotoxicity highlights the need for further risk assessment of TiO2 in consumer products.
Area of Science:
- Environmental Health
- Epigenetics
- Toxicology
Background:
- Titanium dioxide (TiO2) is widely used in consumer products, raising safety concerns due to reported toxicity.
- Epigenetic mechanisms, such as DNA methylation, play a crucial role in biological responses to environmental exposures.
Purpose of the Study:
- To investigate the epigenotoxic effects of titanium dioxide (TiO2) exposure on DNA methylation in human cell lines relevant to exposure.
- To assess the impact of TiO2 on global DNA methylation and specific gene promoter methylation.
Main Methods:
- Utilized Caco-2 (colorectal) and HepG2 (liver) human cell lines for TiO2 exposure studies.
- Assessed global DNA methylation using ELISA-based immunochemical analysis.
- Evaluated gene promoter methylation via EpiTect Methyl II Signature PCR Array and quantified gene expression using qRT-PCR.
Main Results:
- Observed a decrease in global DNA methylation in both Caco-2 and HepG2 cells following TiO2 exposure.
- Identified methylation changes in promoters of seven genes, including TP53 and BNIP3, across cell lines.
- Detected aberrant expression of DNA methyltransferases, MBD2, and UHRF1, correlating with methylation alterations.
Conclusions:
- TiO2 exposure demonstrably affects DNA methylation patterns in human colorectal and liver cells.
- Findings support the role of epigenetics in mediating TiO2's biological effects and toxicity.
- Epigenetic assessments are crucial for a comprehensive evaluation of TiO2's human health risks.
Related Concept Videos
Mutations
31.4K
Mutations are changes in the sequence of DNA. These changes can occur spontaneously or they can be induced by exposure to environmental factors. Mutations can be characterized in a number of different ways: whether and how they alter the amino acid sequence of the protein, whether they occur over a small or large area of DNA, and whether they occur in somatic cells or germline cells.
Chromosomal Alterations Are Large-Scale Mutations
While point mutations are changes in a single nucleotide in...
Chromosomal Alterations Are Large-Scale Mutations
While point mutations are changes in a single nucleotide in...
31.4K
Epigenetic Regulation
2.9K
Epigenetic changes alter the physical structure of the DNA without changing the genetic sequence and often regulate whether genes are turned on or off. This regulation ensures that each cell produces only proteins necessary for its function. For example, proteins that promote bone growth are not produced in muscle cells. Epigenetic mechanisms play an essential role in healthy development. Conversely, precisely regulated epigenetic mechanisms are disrupted in diseases like cancer.
X-chromosome...
X-chromosome...
2.9K
Nucleotide Excision Repair
3.4K
DNA Distortion and Damage
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...
3.4K
Chromatin Modification in iPS Cells
1.6K
Chromatin modification alters gene expression; therefore, scientists can add histone-modifying enzymes, histone variants, and chromatin remodeling complexes to somatic cells to aid reprogramming into pluripotent stem (iPS) cells.
Compact chromatin makes reprogramming difficult. Enzymes, such as histone demethylases and acetyltransferases, are often added during reprogramming to loosen the chromatin, making the DNA more accessible to transcription factors. Molecules that inhibit histone...
Compact chromatin makes reprogramming difficult. Enzymes, such as histone demethylases and acetyltransferases, are often added during reprogramming to loosen the chromatin, making the DNA more accessible to transcription factors. Molecules that inhibit histone...
1.6K
Genomic Imprinting and Inheritance
32.7K
Diploid organisms inherit genetic material through chromosomes from both parents. Copies of the same gene are known as alleles. In most cases, both alleles are simultaneously expressed and allow various cellular processes to function optimally. If one of the alleles is missing or mutated, the expression of the other allele can compensate; however, this is not true for all genes.
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
The expression of some genes depends on which parent passed the gene to the offspring, through a phenomenon known as...
32.7K

