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Updated: May 2, 2026

Murine Model for Non-invasive Imaging to Detect and Monitor Ovarian Cancer Recurrence
Published on: November 2, 2014
Recent technological advances in using mouse models to study ovarian cancer
Carrie Danielle House1, Lidia Hernandez1, Christina Messineo Annunziata1
1Women's Malignancies Branch, National Cancer Institute , Bethesda, MD , USA.
Serous epithelial ovarian cancer (SEOC) remains a lethal gynecological cancer with poor survival rates. Improved preclinical mouse models and imaging techniques offer promise for advancing SEOC research and future clinical trials.
Area of Science:
- Gynecologic Oncology
- Cancer Research
- Translational Medicine
Background:
- Serous epithelial ovarian cancer (SEOC) is the leading cause of gynecologic cancer mortality in the US.
- Disease recurrence significantly contributes to SEOC morbidity and mortality.
- Survival rates for SEOC have stagnated despite advances in understanding molecular mechanisms.
Purpose of the Study:
- To review the development and utility of preclinical mouse models for studying SEOC.
- To highlight advancements in SEOC research methodologies.
- To underscore the potential of improved models for future clinical trial success.
Main Methods:
- Review of existing literature on preclinical ovarian cancer models (xenograft, syngeneic, genetically engineered).
- Discussion of technological advancements, including live animal imaging.
- Analysis of how model improvements enhance understanding of SEOC etiology and dissemination.
Main Results:
- Current preclinical models increasingly mimic human SEOC genotype and phenotype.
- Live animal imaging enables effective monitoring of the tumor microenvironment and therapeutic responses.
- Advancements facilitate deeper insights into SEOC development and treatment resistance.
Conclusions:
- Improved preclinical mouse models are crucial for advancing SEOC research.
- Technological innovations enhance the study and application of these models.
- Enhanced preclinical research is expected to improve outcomes in future SEOC human clinical trials.
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