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Cell transformation and genotoxicity of bis(2,3-dichloro-1-propyl)ether.

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Cell transformation and genotoxicity of bis(2,3-dichloro-1-propyl)ether. / Neurath, G.; Martin, Francis L.; Piasecki, A. et al.
In: Environmental and Molecular Mutagenesis, Vol. 35, No. 4, 2000, p. 312-318.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Neurath, G, Martin, FL, Piasecki, A, Ruge, A, Cole, KJ, Franke, S, Franke, W & Marquardt, H 2000, 'Cell transformation and genotoxicity of bis(2,3-dichloro-1-propyl)ether.', Environmental and Molecular Mutagenesis, vol. 35, no. 4, pp. 312-318. https://doi.org/10.1002/1098-2280(2000)35:4<312::AID-EM5>3.0.CO;2-R

APA

Neurath, G., Martin, F. L., Piasecki, A., Ruge, A., Cole, K. J., Franke, S., Franke, W., & Marquardt, H. (2000). Cell transformation and genotoxicity of bis(2,3-dichloro-1-propyl)ether. Environmental and Molecular Mutagenesis, 35(4), 312-318. https://doi.org/10.1002/1098-2280(2000)35:4<312::AID-EM5>3.0.CO;2-R

Vancouver

Neurath G, Martin FL, Piasecki A, Ruge A, Cole KJ, Franke S et al. Cell transformation and genotoxicity of bis(2,3-dichloro-1-propyl)ether. Environmental and Molecular Mutagenesis. 2000;35(4):312-318. doi: 10.1002/1098-2280(2000)35:4<312::AID-EM5>3.0.CO;2-R

Author

Neurath, G. ; Martin, Francis L. ; Piasecki, A. et al. / Cell transformation and genotoxicity of bis(2,3-dichloro-1-propyl)ether. In: Environmental and Molecular Mutagenesis. 2000 ; Vol. 35, No. 4. pp. 312-318.

Bibtex

@article{a9befe19776d4cef9474d6dcaa6a764a,
title = "Cell transformation and genotoxicity of bis(2,3-dichloro-1-propyl)ether.",
abstract = "Bis(dichloropropyl) ether isomers have been identified in a petrochemical plant effluent through a toxicity identification evaluation study in the United States. They have also been observed in the microgram per liter range along one of the largest rivers in Europe, the Elbe River. In the present investigation, the genotoxic and transforming activity of a bis(dichloropropyl) ether isomer, bis(2,3-dichloro-1-propyl) ether, was assayed in vitro. The results demonstrate that bis(2,3-dichloro-1-propyl) ether is a potent mutagen in Salmonella typhimurium strains TA 100, TA 1535, and to a lesser extent in strain TA 98, but only when tested in the presence of a metabolic activation system (S9 mix). We have also investigated the induction of micronuclei by bis(2,3-dichloro-1-propyl) ether in the metabolically competent cell line, MCL-5. A linear, dose-dependent increase in micronuclei was observed following exposure to bis(2,3-dichloro-1-propyl) ether. The DNA strand-breaking capacity of this chemical was assessed in the alkaline single-cell gel electrophoresis (comet) assay with MCL-5 cells. Bis(2,3-dichloro-1-propyl) ether clearly induced DNA strand breaks in the 4.5-45.5 g/ml dose range. The ether also induced malignant transformation in C3H/M2 mouse fibroblasts after metabolic activation (S9 mix). Thus, it must be suspected that bis(2,3-dichloro-1-propyl) ether may possess a carcinogenic potential. Since the compound along with its isomers is present in considerable concentrations in surface water, their elimination is a matter of significant public concern.",
keywords = "bis(2, 3-dichloro-1-propyl) ether, genotoxicity, Ames test, micronucleus test, comet assay, cell transformation",
author = "G. Neurath and Martin, {Francis L.} and A. Piasecki and A. Ruge and Cole, {Kathleen J.} and S. Franke and W. Franke and H. Marquardt",
year = "2000",
doi = "10.1002/1098-2280(2000)35:4<312::AID-EM5>3.0.CO;2-R",
language = "English",
volume = "35",
pages = "312--318",
journal = "Environmental and Molecular Mutagenesis",
issn = "0893-6692",
publisher = "Wiley-Liss Inc.",
number = "4",

}

RIS

TY - JOUR

T1 - Cell transformation and genotoxicity of bis(2,3-dichloro-1-propyl)ether.

AU - Neurath, G.

AU - Martin, Francis L.

AU - Piasecki, A.

AU - Ruge, A.

AU - Cole, Kathleen J.

AU - Franke, S.

AU - Franke, W.

AU - Marquardt, H.

PY - 2000

Y1 - 2000

N2 - Bis(dichloropropyl) ether isomers have been identified in a petrochemical plant effluent through a toxicity identification evaluation study in the United States. They have also been observed in the microgram per liter range along one of the largest rivers in Europe, the Elbe River. In the present investigation, the genotoxic and transforming activity of a bis(dichloropropyl) ether isomer, bis(2,3-dichloro-1-propyl) ether, was assayed in vitro. The results demonstrate that bis(2,3-dichloro-1-propyl) ether is a potent mutagen in Salmonella typhimurium strains TA 100, TA 1535, and to a lesser extent in strain TA 98, but only when tested in the presence of a metabolic activation system (S9 mix). We have also investigated the induction of micronuclei by bis(2,3-dichloro-1-propyl) ether in the metabolically competent cell line, MCL-5. A linear, dose-dependent increase in micronuclei was observed following exposure to bis(2,3-dichloro-1-propyl) ether. The DNA strand-breaking capacity of this chemical was assessed in the alkaline single-cell gel electrophoresis (comet) assay with MCL-5 cells. Bis(2,3-dichloro-1-propyl) ether clearly induced DNA strand breaks in the 4.5-45.5 g/ml dose range. The ether also induced malignant transformation in C3H/M2 mouse fibroblasts after metabolic activation (S9 mix). Thus, it must be suspected that bis(2,3-dichloro-1-propyl) ether may possess a carcinogenic potential. Since the compound along with its isomers is present in considerable concentrations in surface water, their elimination is a matter of significant public concern.

AB - Bis(dichloropropyl) ether isomers have been identified in a petrochemical plant effluent through a toxicity identification evaluation study in the United States. They have also been observed in the microgram per liter range along one of the largest rivers in Europe, the Elbe River. In the present investigation, the genotoxic and transforming activity of a bis(dichloropropyl) ether isomer, bis(2,3-dichloro-1-propyl) ether, was assayed in vitro. The results demonstrate that bis(2,3-dichloro-1-propyl) ether is a potent mutagen in Salmonella typhimurium strains TA 100, TA 1535, and to a lesser extent in strain TA 98, but only when tested in the presence of a metabolic activation system (S9 mix). We have also investigated the induction of micronuclei by bis(2,3-dichloro-1-propyl) ether in the metabolically competent cell line, MCL-5. A linear, dose-dependent increase in micronuclei was observed following exposure to bis(2,3-dichloro-1-propyl) ether. The DNA strand-breaking capacity of this chemical was assessed in the alkaline single-cell gel electrophoresis (comet) assay with MCL-5 cells. Bis(2,3-dichloro-1-propyl) ether clearly induced DNA strand breaks in the 4.5-45.5 g/ml dose range. The ether also induced malignant transformation in C3H/M2 mouse fibroblasts after metabolic activation (S9 mix). Thus, it must be suspected that bis(2,3-dichloro-1-propyl) ether may possess a carcinogenic potential. Since the compound along with its isomers is present in considerable concentrations in surface water, their elimination is a matter of significant public concern.

KW - bis(2

KW - 3-dichloro-1-propyl) ether

KW - genotoxicity

KW - Ames test

KW - micronucleus test

KW - comet assay

KW - cell transformation

U2 - 10.1002/1098-2280(2000)35:4<312::AID-EM5>3.0.CO;2-R

DO - 10.1002/1098-2280(2000)35:4<312::AID-EM5>3.0.CO;2-R

M3 - Journal article

VL - 35

SP - 312

EP - 318

JO - Environmental and Molecular Mutagenesis

JF - Environmental and Molecular Mutagenesis

SN - 0893-6692

IS - 4

ER -