Characterization and evaluation of pre-clinical suitability of a syngeneic orthotopic mouse ovarian cancer model

Anticancer Res. 2013 Apr;33(4):1317-24.

Abstract

Background/aim: To develop and characterize the pre-clinical suitability of a syngeneic mouse epithelial ovarian cancer model in immunocompetent hosts.

Materials and methods: ID8 mouse ovarian surface epithelium cells were implanted into the left ovarian bursa of C57BL/6 mice. Using conventional as well as ultrasound-based techniques and histopathological analysis, the tumor weights, volumes, metastases, ascites and vascularity were observed over a period of 16 weeks.

Results: Ovarian weights and volume increased 12- and 7-fold, respectively. Ultrasound measurements of ovarian ID8 tumors correlated with the actual size obtained following surgical excision. Ascites and metastasis were first observed at 12 weeks post-orthotopic implantation. Histopathological analysis indicated similarities between orthotopically-generated ovarian tumors and human ovarian tumors. However, there was less evidence of angiogenesis in this animal model.

Conclusion: The development of this mouse model closely replicates characteristics seen in human ovarian cancer with feasibility of using ultrasound to assess tumor formation, progression and vascularization.

Publication types

  • Evaluation Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Ascites / pathology*
  • Biomarkers, Tumor / analysis
  • Carcinoma, Ovarian Epithelial
  • Disease Models, Animal*
  • Disease Progression
  • Female
  • Humans
  • Immunocompromised Host*
  • Immunoenzyme Techniques
  • Mice
  • Mice, Inbred C57BL
  • Microvessels / pathology*
  • Neoplasm Metastasis
  • Neoplasms, Glandular and Epithelial / diagnostic imaging
  • Neoplasms, Glandular and Epithelial / metabolism
  • Neoplasms, Glandular and Epithelial / pathology*
  • Neovascularization, Pathologic / pathology*
  • Ovarian Neoplasms / diagnostic imaging
  • Ovarian Neoplasms / metabolism
  • Ovarian Neoplasms / pathology*
  • Tumor Burden
  • Tumor Cells, Cultured
  • Ultrasonography

Substances

  • Biomarkers, Tumor