Reference SummaryDavis LM, Carcinogenesis 1994 Aug;15(8):1637-45

Title

Loss of heterozygosity in spontaneous and chemically induced tumors of the B6C3F1 mouse.

Authors

Davis LM; Caspary WJ; Sakallah SA; Maronpot R; Wiseman R; Barrett JC; Elliott R; Hozier JC

Journal

Carcinogenesis

Volume

15

Issue

8

Year

1994

Pages

1637-45

Abstract

The B6C3F1 mouse is used worldwide to gauge the carcinogenic hazard posed by chemicals to humans. An assessment of the ability of this rodent model to predict human neoplasia requires an evaluation of similarities and differences in the genetics of tumor formation between these two species. We examined 142 spontaneous and chemically-induced liver tumors isolated from the B6C3F1 mouse for losses of heterozygosity (LOH) at 78 polymorphic loci and compared these results to genetic changes known to occur in human hepatocellular carcinoma. Approximately a third of the 142 mouse tumors exhibited LOH, suggesting that tumor suppressor gene inactivation may be involved in the formation of mouse liver tumors. Most of the LOH observed was restricted to seven chromosome sites and most of the tumors that underwent LOH lost alleles from only one of those seven sites. The relatively few losses seen in these mouse tumors distinguished them from clinical stage human tumors in that, in the mouse tumors, interstitial deletions appeared more frequently than losses of whole chromosomes. Only four mouse tumors lost a whole chromosome. LOH occurred at loci of the mouse genome syntenic to areas of the human genome known to harbor the Wilms', retinoblastoma, APC, MCC and DCC tumor suppressor genes; these genes have never been associated with hepatocellular carcinomas. Losses observed on chromosomes 5 and 8 (syntenic to human chromosomes 4 and 16) suggest tumor suppressor genes that are common to hepatocellular carcinomas from both species, while losses on chromosome 9 suggest involvement of a previously unidentified tumor suppressor gene.

Links

J:19777 – MGI References
8055644 – National Library of Medicine/PubMed

Models

Strain Model Name Treatment Agent(s) Organ Affected Frequency Model Details
(C57BL/6J x C3H/HeJ)F1/J Liver adenoma Liver

observed

(C57BL/6J x C3H/HeJ)F1/J Liver adenoma
  • chlordane
Liver

observed

(C57BL/6J x C3H/HeJ)F1/J Liver adenoma
  • tetrachloroethylene (TCE)
Liver

observed

(C57BL/6J x C3H/HeJ)F1/J Liver carcinoma
  • chlordane
Liver

observed

(C57BL/6J x C3H/HeJ)F1/J Liver carcinoma
  • methylene chloride (MC)
Liver

observed

(C57BL/6J x C3H/HeJ)F1/J Liver carcinoma
  • tetrachloroethylene (TCE)
Liver

observed

(C57BL/6J x C3H/HeJ)F1/J Liver foci Liver

observed

(C57BL/6J x C3H/HeJ)F1/J Liver hepatocellular carcinoma Liver

high

(C57BL/6J x C3H/HeJ)F1/J Liver tumor
  • methylene chloride (MC)
Liver

observed

(C57BL/6J x C3H/HeJ)F1/J Liver tumor
  • vinyl carbamate (VC)
Liver

observed

C3H/HeJ Liver tumor Liver

60

C57BL/6J Liver tumor Liver

observed