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Review
. 2017 Aug;58(3):321-330.
doi: 10.1007/s13353-016-0380-3. Epub 2016 Dec 12.

Polycyclic aromatic hydrocarbons and PAH-related DNA adducts

Affiliations
Review

Polycyclic aromatic hydrocarbons and PAH-related DNA adducts

Błaszczyk Ewa et al. J Appl Genet. 2017 Aug.

Abstract

Investigations on the impact of chemicals on the environment and human health have led to the development of an exposome concept. The exposome refers to the totality of exposures received by a person during life, including exposures to life-style factors, from the prenatal period to death. The exposure to genotoxic chemicals and their reactive metabolites can induce chemical modifications of DNA, such as, for example, DNA adducts, which have been extensively studied and which play a key role in chemically induced carcinogenesis. Development of different methods for the identification of DNA adducts has led to adopting DNA adductomic approaches. The ability to simultaneously detect multiple PAH-derived DNA adducts may allow for the improved assessment of exposure, and offer a mechanistic insight into the carcinogenic process following exposure to PAH mixtures. The major advantage of measuring chemical-specific DNA adducts is the assessment of a biologically effective dose. This review provides information about the occurrence of the polycyclic aromatic hydrocarbons (PAHs) and their influence on human exposure and biological effects, including PAH-derived DNA adduct formation and repair processes. Selected methods used for determination of DNA adducts have been presented.

Keywords: Benzo[a]pyrene; DNA damage; PAH–DNA adducts; Polycyclic aromatic hydrocarbons.

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Conflict of interest statement

Conflict of interest

The authors declare that they have no conflict of interest.

Funding

This publication was developed on the basis of experience gained during realization of the research project no N N404 11073 in the Institute for Ecology of Industrial Areas.

Figures

Fig. 1
Fig. 1
“Bay” and “fjord” regions in different PAH conformations
Fig. 2
Fig. 2
Metabolic activation pathways of benzo[a]pyrene (Lodovici et al. 2004)

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