HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Aflatoxin B1-DNA adduct formation and mutagenicity in livers of neonatal male and female B6C3F1 mice.

Abstract
Exposure to genotoxic chemicals at a young age increases cancer incidence later in life. Aflatoxin B(1) (AFB(1)) is a potent genotoxin that induces hepatocellular carcinoma (HCC) in many animal species and in humans. Whereas adult mice are insensitive to aflatoxin-induced carcinogenesis, mice treated with AFB(1) shortly after birth develop a high incidence of HCC in adulthood. Furthermore, the incidence of HCC in adult male mice treated as infants is much greater than in females, reasons for which are unclear. In this study, treatment with AFB(1) produced similar levels of DNA damage and mutations in the liver of newborn male and female gpt delta B6C3F1 mice. Twenty-four hours after dosing with AFB(1) (6 mg/kg), the highly mutagenic AFB(1)-FAPY adduct was present at twice the level of AFB(1)-N(7)-guanine in liver DNA of males and females. A multiple dose regimen (3 × 2 mg/kg), while delivering the same total dose, resulted in lower AFB(1) adduct levels. Mutation frequencies in the gpt transgene in liver were increased by 20- to 30-fold. The most prominent mutations in AFB(1)-treated mice were G:C to T:A transversions and G:C to A:T transitions. At this 21-day time point, no significant differences were found in mutation frequency or types of mutations between males and females. These results show that infant male and female B6C3F1 mice experience similar amounts of DNA damage and mutation from AFB(1) that may initiate the neoplastic process. The gender difference in the subsequent development of HCC highlights the importance of elucidating additional factors that modulate HCC development.
AuthorsLeslie L Woo, Patricia A Egner, Crystal L Belanger, Roongtiwa Wattanawaraporn, Laura J Trudel, Robert G Croy, John D Groopman, John M Essigmann, Gerald N Wogan, Jason T Bouhenguel
JournalToxicological sciences : an official journal of the Society of Toxicology (Toxicol Sci) Vol. 122 Issue 1 Pg. 38-44 (Jul 2011) ISSN: 1096-0929 [Electronic] United States
PMID21507988 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)
Chemical References
  • DNA Adducts
  • Mutagens
  • aflatoxin B1-DNA adduct
  • Guanine
  • Aflatoxin B1
Topics
  • Aflatoxin B1 (metabolism, toxicity)
  • Age Factors
  • Animals
  • Animals, Newborn
  • Base Sequence
  • Carcinogenicity Tests
  • Carcinoma, Hepatocellular (chemically induced, genetics, pathology)
  • DNA Adducts (metabolism, toxicity)
  • Female
  • Guanine (metabolism)
  • Liver (drug effects, pathology)
  • Liver Neoplasms (chemically induced, genetics, pathology)
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Molecular Sequence Data
  • Mutagens (toxicity)
  • Mutation Rate
  • Sequence Analysis, DNA
  • Sex Factors

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: