• 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,

. 2011 ; 714 (1-2) : 53-62. [pub] 20110705

Jazyk angličtina Země Nizozemsko

Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/bmc12028170

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.

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

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...