Manganese inhibition of sarcoma induction by benzo[a]pyrene in rats

F W Sunderman1, K S McCully, S B Taubman

  • 1Department of Laboratory Medicine, University of Connecticut School of Medicine, Farmington 06032, USA.

Carcinogenesis
|July 1, 1980
PubMed

Insights

Manganese (Mn) dust inhibits benzo[a]pyrene (BP) carcinogenicity in rats, while chromium (Cr) dust enhances it. Mn dust did not affect 7,12-dimethylbenz[a]anthracene (DMBA) carcinogenicity.

Area of Science:

  • Toxicology and Carcinogenesis
  • Environmental Health
  • Occupational Exposure

Background:

  • Polycyclic aromatic hydrocarbons (PAHs) are known carcinogens.
  • Industrial dusts, such as manganese (Mn) and chromium (Cr), are common occupational and environmental exposures.
  • The combined effects of PAHs and metal dusts on carcinogenesis are not fully understood.

Purpose of the Study:

  • To investigate the effects of Mn and Cr dusts on the carcinogenicity of benzo[a]pyrene (BP) and 7,12-dimethylbenz[a]anthracene (DMBA) in male Fischer 344 rats.
  • To determine if Mn or Cr dusts modulate PAH-induced tumor formation.

Main Methods:

  • Male Fischer 344 rats received intramuscular injections of BP or DMBA, alone or in combination with Mn dust or Cr dust.
  • Tumor (sarcoma) incidence at the injection site was monitored over 100 weeks.
  • Control groups received vehicle, Mn dust alone, or Cr dust alone.

Main Results:

  • Mn dust significantly inhibited BP-induced sarcoma formation (17/20 vs. 10/19 rats, P < 0.05 in Exp I; 17/20 vs. 5/17 rats, P < 0.001 in Exp II).
  • Cr dust significantly enhanced BP-induced sarcoma formation (17/20 vs. 20/20 rats).
  • Mn dust did not affect DMBA carcinogenicity, and Cr dust did not affect BP or DMBA carcinogenicity.

Conclusions:

  • Mn dust exhibits an inhibitory effect on BP carcinogenicity when co-administered via single intramuscular injection.
  • Cr dust potentiates the carcinogenic effects of BP.
  • The interaction between metal dusts and PAHs is specific, with Mn and Cr showing distinct modulatory roles.