-
Je něco špatně v tomto záznamu ?
Activation of the aryl hydrocarbon receptor is the major toxic mode of action of an organic extract of a reference urban dust particulate matter mixture: the role of polycyclic aromatic hydrocarbons
Z. Andrysík, J. Vondráček, S. Marvanová, M. Ciganek, J. Neča, K. Pěnčíková, B. Mahadevan, J. Topinka, WM. Baird, A. Kozubík, M. Machala,
Jazyk angličtina Země Nizozemsko
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
- MeSH
- adukty DNA účinky léků MeSH
- apoptóza účinky léků MeSH
- buněčné linie MeSH
- cytochrom P-450 CYP1A1 metabolismus MeSH
- geny p53 účinky léků MeSH
- játra účinky léků MeSH
- krysa rodu rattus MeSH
- mutageny toxicita MeSH
- organické látky toxicita MeSH
- pevné částice toxicita MeSH
- polycyklické aromatické uhlovodíky toxicita MeSH
- poškození DNA účinky léků MeSH
- proliferace buněk účinky léků MeSH
- receptory aromatických uhlovodíků metabolismus MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
Many of the toxic and carcinogenic effects of urban air pollution have been linked to polycyclic aromatic hydrocarbons (PAHs) adsorbed to airborne particulate matter (PM). The carcinogenic properties of PAHs in complex organic mixtures derived from PM have been chiefly attributed to their mutagenicity. Nevertheless, PAHs are also potent activators of the aryl hydrocarbon receptor (AhR), which may contribute to their nongenotoxic effects, including tumor promotion. As the genotoxicity of carcinogenic PAHs in complex mixtures derived from urban PM is often inhibited by other mixture constituents, the AhR-mediated activity of urban PM extracts might significantly contribute to the carcinogenic activity of such mixtures. In the present study, we used an organic extract of the urban dust standard reference material, SRM1649a, as a model mixture to study a range of toxic effects related to DNA damage and AhR activation. Both the organic extract and its neutral aromatic fraction formed a low number of DNA adducts per nucleotide in the liver epithelial WB-F344 cells model, without inducing DNA damage response, such as tumor suppressor p53 activation and apoptosis. In contrast, we found that this extract, as well as its neutral and polar fractions, were potent inducers of a range of AhR-mediated responses, including induction of the AhR-mediated transcription, such as cytochrome P450 1A1/1B1 expression, and the AhR-dependent cell proliferation. Importantly, these toxic events occurred at doses one order of magnitude lower than DNA damage. The AhR-mediated activity of the neutral fraction was linked to PAHs and their derivatives, as polychlorinated dibenzo-p-dioxins, dibenzofurans and biphenyls were only minor contributors to the overall AhR-mediated activity. Taken together, our data suggest that more attention should be paid to the AhR-dependent nongenotoxic events elicited by urban PM constituents, especially PAHs and their derivatives.
Department of Cytokinetics Institute of Biophysics AS CR Královopolská 135 61265 Brno Czech Republic
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc12028170
- 003
- CZ-PrNML
- 005
- 20121210094030.0
- 007
- ta
- 008
- 120817e20110705ne f 000 0#eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.mrfmmm.2011.06.011 $2 doi
- 035 __
- $a (PubMed)21762708
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a ne
- 100 1_
- $a Andrysík, Zdeněk $u Department of Cytokinetics, Institute of Biophysics AS CR, Královopolská 135, 61265 Brno, Czech Republic. $7 xx0072995
- 245 10
- $a Activation of the aryl hydrocarbon receptor is the major toxic mode of action of an organic extract of a reference urban dust particulate matter mixture: the role of polycyclic aromatic hydrocarbons / $c Z. Andrysík, J. Vondráček, S. Marvanová, M. Ciganek, J. Neča, K. Pěnčíková, B. Mahadevan, J. Topinka, WM. Baird, A. Kozubík, M. Machala,
- 520 9_
- $a Many of the toxic and carcinogenic effects of urban air pollution have been linked to polycyclic aromatic hydrocarbons (PAHs) adsorbed to airborne particulate matter (PM). The carcinogenic properties of PAHs in complex organic mixtures derived from PM have been chiefly attributed to their mutagenicity. Nevertheless, PAHs are also potent activators of the aryl hydrocarbon receptor (AhR), which may contribute to their nongenotoxic effects, including tumor promotion. As the genotoxicity of carcinogenic PAHs in complex mixtures derived from urban PM is often inhibited by other mixture constituents, the AhR-mediated activity of urban PM extracts might significantly contribute to the carcinogenic activity of such mixtures. In the present study, we used an organic extract of the urban dust standard reference material, SRM1649a, as a model mixture to study a range of toxic effects related to DNA damage and AhR activation. Both the organic extract and its neutral aromatic fraction formed a low number of DNA adducts per nucleotide in the liver epithelial WB-F344 cells model, without inducing DNA damage response, such as tumor suppressor p53 activation and apoptosis. In contrast, we found that this extract, as well as its neutral and polar fractions, were potent inducers of a range of AhR-mediated responses, including induction of the AhR-mediated transcription, such as cytochrome P450 1A1/1B1 expression, and the AhR-dependent cell proliferation. Importantly, these toxic events occurred at doses one order of magnitude lower than DNA damage. The AhR-mediated activity of the neutral fraction was linked to PAHs and their derivatives, as polychlorinated dibenzo-p-dioxins, dibenzofurans and biphenyls were only minor contributors to the overall AhR-mediated activity. Taken together, our data suggest that more attention should be paid to the AhR-dependent nongenotoxic events elicited by urban PM constituents, especially PAHs and their derivatives.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a apoptóza $x účinky léků $7 D017209
- 650 _2
- $a buněčné linie $7 D002460
- 650 _2
- $a proliferace buněk $x účinky léků $7 D049109
- 650 _2
- $a cytochrom P-450 CYP1A1 $x metabolismus $7 D019363
- 650 _2
- $a adukty DNA $x účinky léků $7 D018736
- 650 _2
- $a poškození DNA $x účinky léků $7 D004249
- 650 _2
- $a vztah mezi dávkou a účinkem léčiva $7 D004305
- 650 _2
- $a geny p53 $x účinky léků $7 D016158
- 650 _2
- $a játra $x účinky léků $7 D008099
- 650 _2
- $a mutageny $x toxicita $7 D009153
- 650 _2
- $a organické látky $x toxicita $7 D009930
- 650 _2
- $a pevné částice $x toxicita $7 D052638
- 650 _2
- $a polycyklické aromatické uhlovodíky $x toxicita $7 D011084
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a receptory aromatických uhlovodíků $x metabolismus $7 D018336
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a Research Support, N.I.H., Extramural $7 D052061
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Vondráček, Jan
- 700 1_
- $a Marvanová, Soňa
- 700 1_
- $a Ciganek, Miroslav
- 700 1_
- $a Neča, Jiří
- 700 1_
- $a Pěnčíková, Kateřina
- 700 1_
- $a Mahadevan, Brinda
- 700 1_
- $a Topinka, Jan
- 700 1_
- $a Baird, William M
- 700 1_
- $a Kozubík, Alois
- 700 1_
- $a Machala, Miroslav
- 773 0_
- $w MED00003430 $t Mutation research $x 0027-5107 $g Roč. 714, č. 1-2 (20110705), s. 53-62
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/21762708 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y m
- 990 __
- $a 20120817 $b ABA008
- 991 __
- $a 20121210094107 $b ABA008
- 999 __
- $a ok $b bmc $g 950212 $s 785516
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2011 $b 714 $c 1-2 $d 53-62 $e 20110705 $i 0027-5107 $m Mutation research $n Mutat Res $x MED00003430
- LZP __
- $a Pubmed-20120817/11/04