1980
DOI: 10.1016/0045-6535(80)90093-4
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Evidence for nitroaromatics as direct-acting mutagens of airborne particulates

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Cited by 126 publications
(21 citation statements)
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“…Tester strains deficient in "classical" nitroreductases are less susceptible to mutation induction by 1-nitropyrene (19,54,57,58). The reduction of 1-nitropyrene is accomplished by a bacterial nitroreductase that is distinct from the "classical" nitroreductase that catalyzes the conversion of nitrofurans, nitroimidazoles, and simple nitroarenes (e.g., nitronaphthalenes, nitrofluorenes) to mutagens (54,55,58).…”
Section: Nitropolynuclear Aromatic Hydrocarbonsmentioning
confidence: 99%
“…Tester strains deficient in "classical" nitroreductases are less susceptible to mutation induction by 1-nitropyrene (19,54,57,58). The reduction of 1-nitropyrene is accomplished by a bacterial nitroreductase that is distinct from the "classical" nitroreductase that catalyzes the conversion of nitrofurans, nitroimidazoles, and simple nitroarenes (e.g., nitronaphthalenes, nitrofluorenes) to mutagens (54,55,58).…”
Section: Nitropolynuclear Aromatic Hydrocarbonsmentioning
confidence: 99%
“…43) Nitropolycyclic aromatic hydrocarbons (nitroPAHs), which are carcinogenic and mutagenic, enter the environment from diesel engine exhaust, urban pollution sources, cigarette smoking and so on. [44][45][46] Several reports have indicated that nitroPAHs are mainly metabolized by nitro reduction, ring hydroxylation, acylation and conjugation in mammalian species. 47) Nitro-PAHs should also be examined to see whether nitro reduction or hydroxylation of the aromatic rings activates these compounds to xenobiotic estrogens, as is the case for their carcinogenicity.…”
Section: Activation Of Polycyclic Aromatic Hydrocarbons and Nitropolymentioning
confidence: 99%
“…However, more convincing was the demonstration of the potent mutagenicity of the reduction product of 1,8-dinitropyrene in strain TA98/1,8-DNP6 (Table XVII). The strain, normally is non-responsive to (55,67) with nitro-and hydroxyl amino-naphthalenes using strains deficient in the classical nitroreductases (Table XVIII).…”
mentioning
confidence: 99%