Literature DB >> 3816740

Carcinogenicity of chlorinated methane and ethane compounds administered in drinking water to mice.

J E Klaunig, R J Ruch, M A Pereira.   

Abstract

The chlorinated hydrocarbons chloroform (CHCl3), 1,1-dichlorethane (1,1-DCE) and 1,2-dichloroethane (1,2-DCE) have been detected in finished drinking water. When administered to B6C3F1 mice by gavage in corn oil, these compounds have been shown to induce hepatic tumors. The present study examines the effect on liver tumor incidence of continuous treatment of CHCl3 (600 mg/L and 1800 mg/L), 1,1-DCE (835 mg/L and 2500 mg/L), and 1,2-DCE (835 mg/L and 2500 mg/L) administered in drinking water to male B6C3F1 mice using a two-stage (initiation/promotion) treatment protocol. Seventy 4-week-old male B6C3F1 mice constituted each treatment group. Of these mice, 35 were initiated by treatment with diethylnitrosamine (DENA) (10 mg/L) in the drinking water for 4 weeks. The remaining 35 received deionized drinking water. Each group was subsequently treated with one of two concentrations of CHCl3, 1,1-DCE, or 1,2-DCE in drinking water for 52 weeks. An additional group received phenobarbital (PB) (500 mg/L) and served as the positive control for liver tumor promotion. Mice were sampled after 24 weeks (10 mice) and 52 weeks (25 mice). At sampling, liver and lung tumors were detected. None of the compounds increased the number or incidence of lung or liver tumors by themselves. PB promoted liver tumor formation (but not lung tumors) in the DENA-initiated mice. 1,1-DCE and 1,2-DCE did not affect the incidence or number of liver or lung tumors in the DENA-initiated animals. CHCl3, however, inhibited liver and lung tumorigenesis in the DENA-initiated mice.

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Year:  1986        PMID: 3816740      PMCID: PMC1474300          DOI: 10.1289/ehp.866989

Source DB:  PubMed          Journal:  Environ Health Perspect        ISSN: 0091-6765            Impact factor:   9.031


  6 in total

Review 1.  Ethylene dichloride: a review of its metabolism, mutagenic and carcinogenic potential.

Authors:  I W Davidson; D D Sumner; J C Parker
Journal:  Drug Chem Toxicol       Date:  1982       Impact factor: 3.356

2.  In vivo genotoxicity and acute hepatotoxicity of 1,2-dichloroethane in mice: comparison of oral, intraperitoneal, and inhalation routes of exposure.

Authors:  R D Storer; N M Jackson; R B Conolly
Journal:  Cancer Res       Date:  1984-10       Impact factor: 12.701

3.  Application of quantitative stereology to the evaluation of enzyme-altered foci in rat liver.

Authors:  H A Campbell; H C Pitot; V R Potter; B A Laishes
Journal:  Cancer Res       Date:  1982-02       Impact factor: 12.701

4.  Carcinogenicity studies on halogenated hydrocarbons.

Authors:  E K Weisburger
Journal:  Environ Health Perspect       Date:  1977-12       Impact factor: 9.031

5.  Environmental health sciences center task force review on halogenated organics in drinking water.

Authors:  M Deinzer; F Schaumburg; E Klein
Journal:  Environ Health Perspect       Date:  1978-06       Impact factor: 9.031

6.  Trihalomethanes as initiators and promoters of carcinogenesis.

Authors:  M A Pereira; L H Lin; J M Lippitt; S L Herren
Journal:  Environ Health Perspect       Date:  1982-12       Impact factor: 9.031

  6 in total
  2 in total

1.  Circulating mitochondrial DNA as biomarker linking environmental chemical exposure to early preclinical lesions elevation of mtDNA in human serum after exposure to carcinogenic halo-alkane-based pesticides.

Authors:  Lygia T Budnik; Stefan Kloth; Xaver Baur; Alexandra M Preisser; Heidi Schwarzenbach
Journal:  PLoS One       Date:  2013-05-31       Impact factor: 3.240

2.  Biological Basis of Differential Susceptibility to Hepatocarcinogenesis among Mouse Strains.

Authors:  Robert R Maronpot
Journal:  J Toxicol Pathol       Date:  2009-04-06       Impact factor: 1.628

  2 in total

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