Spontaneous and Radiation-induced Mammary and Thyroid Tumorigenesis in LEW and (SD×COP)F1 Brca1 L63X/+ Rats

Anticancer Res. 2025 Nov;45(11):4869-4880. doi: 10.21873/anticanres.17834.

Abstract

Background/aim: Carriers of germline mutations in BRCA1/2 have an increased risk of carcinogenesis in breast, ovary, pancreas, stomach, etc. We previously established the Brca1 mutant (Brca1 L63X/+) rat model on a Sprague-Dawley (SD) background, and it displayed an increased risk of mammary carcinoma during middle age after γ-ray exposure at 7 weeks of age. At younger ages, this model showed no increased risk of mammary tumors or other tumors, probably because of the relatively high susceptibility of the SD background to radiation-induced mammary carcinogenesis. Thus, we established new Brca1 L63X/+ rat models on backgrounds with less susceptibility to mammary carcinogenesis and elucidated tumor risk in mammary tissue and other organs.

Materials and methods: Female Brca1 L63X/+ rats and wild-type (WT) littermates on the LEW background or the F1 hybrid between Copenhagen and SD [(SD×COP)F1] were whole-body irradiated with γ rays at age 7 weeks or left non-irradiated. The rats were palpated weekly, and tumors reaching ~2 cm were biopsied and diagnosed. Rats that were identified as having mammary carcinoma or showing general deterioration were autopsied, and mammary tumors and other tissues, including thyroid, were analyzed for pathology.

Results: The incidence of mammary carcinomas was similar between Brca1 L63X/+ and WT rats on the LEW or (SD×COP)F1 background. Non-irradiated Brca1 L63X/+ rats on the LEW background had significantly higher prevalence of thyroid tumors than non-irradiated WT rats. WT rats tended to have increased prevalence of thyroid carcinoma after radiation exposure, but the prevalence did not differ between irradiated Brca1 L63X/+ and WT rats.

Conclusion: Brca1 L63X/+ rats on the LEW and (SD×COP)F1 backgrounds did not recapitulate the human breast carcinogenesis phenotype. Notably, our findings suggest that a germline mutation in Brca1 increases the prevalence of spontaneous thyroid tumors.

Keywords: BRCA1; animal model; breast cancer; radiation; thyroid tumor.

MeSH terms

  • Animals
  • BRCA1 Protein* / genetics
  • Carcinogenesis / genetics
  • Carcinogenesis / radiation effects
  • Disease Models, Animal
  • Female
  • Gamma Rays / adverse effects
  • Germ-Line Mutation
  • Mammary Neoplasms, Experimental* / etiology
  • Mammary Neoplasms, Experimental* / genetics
  • Mammary Neoplasms, Experimental* / pathology
  • Neoplasms, Radiation-Induced* / genetics
  • Neoplasms, Radiation-Induced* / pathology
  • Rats
  • Rats, Sprague-Dawley
  • Thyroid Neoplasms* / etiology
  • Thyroid Neoplasms* / genetics
  • Thyroid Neoplasms* / pathology

Substances

  • BRCA1 Protein