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Published on: March 20, 2018
Titanium dioxide nanoparticles as guardian against environmental carcinogen benzo[alpha]pyrene
Anupam Dhasmana1, Qazi Mohd Sajid Jamal1, Snober Shabnam Mir1
1Environmental Carcinogenesis and Toxicoinformatics Laboratory, Department of Bioengineering & Biosciences, Integral University, Lucknow, Uttar Pradesh, India.
Titanium dioxide nanoparticles (TiO2 NPs) protect against Benzo[alpha]Pyrene (BaP) toxicity by binding to the AHR receptor, preventing BaP entry into cells. This significantly reduces BaP
Area of Science:
- Environmental Science
- Toxicology
- Nanotechnology
Background:
- Polycyclic aromatic hydrocarbons (PAHs), such as Benzo[alpha]Pyrene (BaP), are known carcinogens linked to lung cancer.
- Titanium dioxide nanoparticles (TiO2 NPs) can adsorb PAHs from environmental matrices like soil and water.
Purpose of the Study:
- To investigate the protective potential of TiO2 NPs against BaP-induced toxicity in a biological system.
- To elucidate the mechanism by which TiO2 NPs confer protection against BaP.
Main Methods:
- A549 cells were co-exposed to varying concentrations of BaP and TiO2 NPs.
- Cellular toxicity was assessed using Micronucleus Assay, MTT Assay, and Reactive Oxygen Species (ROS) Assay.
- In silico molecular docking studies were performed to analyze the interaction between BaP, TiO2 NPs, and the Aryl hydrocarbon receptor (AHR).
Main Results:
- TiO2 NPs significantly reduced the toxic effects of BaP on A549 cells.
- In silico studies revealed that TiO2 NPs have a higher binding affinity to AHR than BaP.
- BaP demonstrated strong adsorption to TiO2 NPs when both were bound to AHR, rather than binding to the original AHR site.
Conclusions:
- TiO2 NPs effectively protect cells from BaP-induced toxicity.
- The protective mechanism involves TiO2 NPs preferentially binding to AHR, thereby blocking BaP entry into cells.
- These findings highlight the potential of TiO2 NPs as a protective agent against PAH-induced cellular damage.
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