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An Orthotopic Model of Serous Ovarian Cancer in Immunocompetent Mice for in vivo Tumor Imaging and Monitoring of Tumor Immune Responses
Published on: November 28, 2010
Orthotopic Model of Ovarian Cancer
Alessandra Decio1, Raffaella Giavazzi2
1Department of Oncology, Laboratory of Biology and Treatment of Metastasis, IRCCS - Istituto di Ricerche Farmacologiche Mario Negri, Via Giuseppe La Masa 19, 20156, Milan, Italy.
Abstract:
Epithelial ovarian cancer (EOC) is the fifth commonest cancer-related cause of female death in the developed world. In spite of current surgical and chemotherapeutic options the vast majority of patients have widely metastatic disease and the survival rate has not much changed over the last years. The anti-angiogenic drugs are driving the field of agents targeting the tumor microenvironment in ovarian cancer. Preclinical models that accurately reproduce the molecular and biological features of ovarian cancer patients are a valuable means of producing reliable data on personalized medicine and predicting the therapeutic response in clinical trials.In this methodological chapter we describe the orthotopic model of ovarian cancer implanted under the ovarian bursa of mice. In spite of anatomical differences between the rodent and human bursa-fallopian tube, the appropriate primary tumor microenvironment at the site of the implant allows investigation of tumor-stroma interactions (e.g., angiogenesis), and is well suited for studying the tumor dissemination and metastasis typical of this disease.This model-although fairly labor intensive-may be useful for assessing novel, more selective therapeutic interventions and for biomarker discovery, reflecting the behavior of this disease.
Insights
This study details an orthotopic mouse model for epithelial ovarian cancer (EOC) research. This model aids in understanding tumor microenvironment interactions and metastasis for developing new ovarian cancer therapies.
Area of Science:
- Oncology
- Cancer Biology
- Preclinical Models
Background:
- Epithelial ovarian cancer (EOC) remains a leading cause of cancer death in women, with limited survival improvements despite current treatments.
- Metastatic disease is common at diagnosis, highlighting the need for better therapeutic strategies and predictive models.
- Targeting the tumor microenvironment, particularly angiogenesis, is a key focus for novel ovarian cancer treatments.
Purpose of the Study:
- To describe and validate an orthotopic mouse model for studying epithelial ovarian cancer.
- To assess the utility of this model for investigating tumor-stroma interactions, angiogenesis, and metastasis.
- To evaluate the model's potential for personalized medicine, therapeutic response prediction, and biomarker discovery.
Main Methods:
- Establishment of an orthotopic epithelial ovarian cancer model by implanting tumor cells under the ovarian bursa of mice.
- Characterization of the tumor microenvironment at the implant site to mimic human disease conditions.
- Utilizing the model to study tumor dissemination, metastasis, and interactions with the tumor stroma.
Main Results:
- The orthotopic model successfully recreates key aspects of the ovarian cancer microenvironment, including angiogenesis.
- The model facilitates the study of tumor-stroma interactions and the metastatic process characteristic of EOC.
- Despite being labor-intensive, the model provides a valuable platform for preclinical research.
Conclusions:
- The described orthotopic ovarian cancer model is a valuable tool for preclinical research, offering insights into tumor biology and metastasis.
- This model can aid in the assessment of novel therapeutic interventions and the discovery of predictive biomarkers for ovarian cancer.
- Further research utilizing this model can contribute to the development of more effective and personalized treatments for epithelial ovarian cancer.
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