Oxidative damage to DNA and repair induced by Norwegian wood smoke particles in human A549 and THP-1 cell lines

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Oxidative damage to DNA and repair induced by Norwegian wood smoke particles in human A549 and THP-1 cell lines. / Danielsen, Pernille Høgh; Loft, Steffen; Kocbach, Anette; Schwarze, Per E; Møller, Peter.

In: Mutation Research - Genetic Toxicology and Environmental Mutagenesis, Vol. 674, No. 1-2, 2009, p. 116-22.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Danielsen, PH, Loft, S, Kocbach, A, Schwarze, PE & Møller, P 2009, 'Oxidative damage to DNA and repair induced by Norwegian wood smoke particles in human A549 and THP-1 cell lines', Mutation Research - Genetic Toxicology and Environmental Mutagenesis, vol. 674, no. 1-2, pp. 116-22. https://doi.org/10.1016/j.mrgentox.2008.10.014

APA

Danielsen, P. H., Loft, S., Kocbach, A., Schwarze, P. E., & Møller, P. (2009). Oxidative damage to DNA and repair induced by Norwegian wood smoke particles in human A549 and THP-1 cell lines. Mutation Research - Genetic Toxicology and Environmental Mutagenesis, 674(1-2), 116-22. https://doi.org/10.1016/j.mrgentox.2008.10.014

Vancouver

Danielsen PH, Loft S, Kocbach A, Schwarze PE, Møller P. Oxidative damage to DNA and repair induced by Norwegian wood smoke particles in human A549 and THP-1 cell lines. Mutation Research - Genetic Toxicology and Environmental Mutagenesis. 2009;674(1-2):116-22. https://doi.org/10.1016/j.mrgentox.2008.10.014

Author

Danielsen, Pernille Høgh ; Loft, Steffen ; Kocbach, Anette ; Schwarze, Per E ; Møller, Peter. / Oxidative damage to DNA and repair induced by Norwegian wood smoke particles in human A549 and THP-1 cell lines. In: Mutation Research - Genetic Toxicology and Environmental Mutagenesis. 2009 ; Vol. 674, No. 1-2. pp. 116-22.

Bibtex

@article{56af41501eba11deb43e000ea68e967b,
title = "Oxidative damage to DNA and repair induced by Norwegian wood smoke particles in human A549 and THP-1 cell lines",
abstract = "Genotoxic effects of traffic-generated particulate matter (PM) are well described, whereas little data are available on PM from combustion of biomass and wood, which contributes substantially to air pollution world wide. The aim of this study was to compare the genotoxicity of wood smoke particulate matter (WSPM), authentic traffic-generated particles, mineral PM and standard reference material (SRM2975) of diesel exhaust particles in human A549 lung epithelial and THP-1 monocytic cell lines. DNA damage was measured as strand breaks (SB) and formamidopyrimidine DNA glycosylase (FPG) sites by the comet assay, whereas cell cytotoxicity was determined as lactate dehydrogenase release. The exposure to WSPM generated SB and FPG sites in both cell lines at concentrations from 2.5 or 25mug/ml, which were not cytotoxic. Compared to all other studied particles, WSPM generated greater responses in terms of both SB and FPG sites. Organic extracts of WSPM and SRM2975 elicited higher levels of SB than native and washed PM at 25 and 100mug/ml, whereas assay saturation precluded reliable assessment of FPG sites. During a 6h post-exposure period, in which the medium with PM had been replaced by fresh medium, 60% of the DNA lesions generated by WSPM were removed. In conclusion, WSPM generated more DNA damage than traffic-generated PM per unit mass in human cell lines, possibly due to the high level of polycyclic aromatic hydrocarbons in WSPM. This suggests that exposure to WSPM might be more hazardous than PM collected from vehicle exhaust with respect to development of lung cancer.",
author = "Danielsen, {Pernille H{\o}gh} and Steffen Loft and Anette Kocbach and Schwarze, {Per E} and Peter M{\o}ller",
year = "2009",
doi = "10.1016/j.mrgentox.2008.10.014",
language = "English",
volume = "674",
pages = "116--22",
journal = "Mutation Research - Genetic Toxicology and Environmental Mutagenesis",
issn = "1383-5718",
publisher = "Elsevier",
number = "1-2",

}

RIS

TY - JOUR

T1 - Oxidative damage to DNA and repair induced by Norwegian wood smoke particles in human A549 and THP-1 cell lines

AU - Danielsen, Pernille Høgh

AU - Loft, Steffen

AU - Kocbach, Anette

AU - Schwarze, Per E

AU - Møller, Peter

PY - 2009

Y1 - 2009

N2 - Genotoxic effects of traffic-generated particulate matter (PM) are well described, whereas little data are available on PM from combustion of biomass and wood, which contributes substantially to air pollution world wide. The aim of this study was to compare the genotoxicity of wood smoke particulate matter (WSPM), authentic traffic-generated particles, mineral PM and standard reference material (SRM2975) of diesel exhaust particles in human A549 lung epithelial and THP-1 monocytic cell lines. DNA damage was measured as strand breaks (SB) and formamidopyrimidine DNA glycosylase (FPG) sites by the comet assay, whereas cell cytotoxicity was determined as lactate dehydrogenase release. The exposure to WSPM generated SB and FPG sites in both cell lines at concentrations from 2.5 or 25mug/ml, which were not cytotoxic. Compared to all other studied particles, WSPM generated greater responses in terms of both SB and FPG sites. Organic extracts of WSPM and SRM2975 elicited higher levels of SB than native and washed PM at 25 and 100mug/ml, whereas assay saturation precluded reliable assessment of FPG sites. During a 6h post-exposure period, in which the medium with PM had been replaced by fresh medium, 60% of the DNA lesions generated by WSPM were removed. In conclusion, WSPM generated more DNA damage than traffic-generated PM per unit mass in human cell lines, possibly due to the high level of polycyclic aromatic hydrocarbons in WSPM. This suggests that exposure to WSPM might be more hazardous than PM collected from vehicle exhaust with respect to development of lung cancer.

AB - Genotoxic effects of traffic-generated particulate matter (PM) are well described, whereas little data are available on PM from combustion of biomass and wood, which contributes substantially to air pollution world wide. The aim of this study was to compare the genotoxicity of wood smoke particulate matter (WSPM), authentic traffic-generated particles, mineral PM and standard reference material (SRM2975) of diesel exhaust particles in human A549 lung epithelial and THP-1 monocytic cell lines. DNA damage was measured as strand breaks (SB) and formamidopyrimidine DNA glycosylase (FPG) sites by the comet assay, whereas cell cytotoxicity was determined as lactate dehydrogenase release. The exposure to WSPM generated SB and FPG sites in both cell lines at concentrations from 2.5 or 25mug/ml, which were not cytotoxic. Compared to all other studied particles, WSPM generated greater responses in terms of both SB and FPG sites. Organic extracts of WSPM and SRM2975 elicited higher levels of SB than native and washed PM at 25 and 100mug/ml, whereas assay saturation precluded reliable assessment of FPG sites. During a 6h post-exposure period, in which the medium with PM had been replaced by fresh medium, 60% of the DNA lesions generated by WSPM were removed. In conclusion, WSPM generated more DNA damage than traffic-generated PM per unit mass in human cell lines, possibly due to the high level of polycyclic aromatic hydrocarbons in WSPM. This suggests that exposure to WSPM might be more hazardous than PM collected from vehicle exhaust with respect to development of lung cancer.

U2 - 10.1016/j.mrgentox.2008.10.014

DO - 10.1016/j.mrgentox.2008.10.014

M3 - Journal article

C2 - 19041418

VL - 674

SP - 116

EP - 122

JO - Mutation Research - Genetic Toxicology and Environmental Mutagenesis

JF - Mutation Research - Genetic Toxicology and Environmental Mutagenesis

SN - 1383-5718

IS - 1-2

ER -

ID: 11688360