Regular article
Carcinogenicity of chloroform in drinking water to male Osborne-Mendel rats and female B6C3F1 mice

https://doi.org/10.1016/0272-0590(85)90200-3Get rights and content

Abstract

The carcinogenic activity of chloroform administered at 0, 200, 400, 900, and 1800 mg/liter in drinking water was studied in male Osborne-Mendel rats and female B6C3F1 mice. A second control group was included in the study and was restricted to the water consumption of the high-dose group. Animals were maintained on study for 104 weeks. Group sizes were adjusted at low doses such that a detectable tumor response would result at the lowest dose if there was a linear relationship with dose, and the higher doses produced responses similar to previous carcinogenesis bioassays of chloroform. The primary finding was that chloroform increased the yield of renal tubular adenomas and adenocarcinomas in male rats in a dose-related manner. For the high-dose group, which corresponded to a time-weighted average dose of 160 mg/kg per day for 104 weeks, there was a 14% incidence of renal tubular adenomas and adenocarcinomas, vs 1% in the control group. This compares to a 24% incidence observed when 180 mg/kg per day of chloroform was administered for 78 weeks in earlier studies. In contrast, chloroform in the drinking water of mice failed to increase the incidence of hepatocellular carcinomas in female B6C3F1 mice. The highest dose group received a time-weighted average dose of 263 mg/kg for 104 weeks, resulting in a 5% combined incidence of hepatocellular adenoma and carcinoma relative to a 6% incidence in the control groups. In a prior National Cancer Institute study an 80% incidence of hepatocellular carcinomas was observed at 270 mg/kg per day for 78 weeks. These data indicate that chloroform administered in drinking water is capable of inducing cancer in the rat kidney. However, the lack of response in the mouse liver when chloroform is supplied in the drinking water suggests that earlier reports of chloroform hepatocarcinogenesis may be related to some interaction with the mode of administration (corn oil gavage).

References (15)

  • Armed Forces Institute of Pathology
  • T.A. Bellar et al.

    The occurrence of organohalides in chlorinated drinking waters

    J. Amer. Water Works Assoc.

    (1974)
  • A.B. Eschenbrenner et al.

    Induction of hepatomas in mice by repeated oral administration of chloroform with observations on sex differences

    J. Natl. Cancer Inst.

    (1945)
  • J.K. Haseman et al.

    Use of historical control data in carcinogenesis studies in rodents

    Toxicol. Pathol.

    (1984)
  • P.A. Mills et al.

    Elution solvent system for florisil column cleanup in organochlorine pesticide residue analyses

    J. Assoc. Off. Anal. Chem.

    (1972)
  • National Cancer Institute (NCI)

    National Cancer Institute Carcinogenesis Bioassay of Chloroform

    (1976)
  • National Cancer Institute (NCI)

    Guidelines for Carcinogen Bioassay in Small Rodents

    (1976, February)
There are more references available in the full text version of this article.

Cited by (0)

View full text