Subcutaneous model |
|
√ Easy to perform |
√ Model is not physiologically relevant |
√ Suitable for monitoring tumor growth |
√ Absence of tumor microenvironment |
√ Low variability in tumor size |
√ Not suitable for studying angiogenesis |
√ Good for routine evaluation of drug efficiency |
√ Not suitable for studying tumor dissemination |
√ Low cost |
|
Intraperitoneal model |
|
√ Easy to perform |
√ Tumor growth measurements require advanced methods |
√ Good model for studying late stages of EOC |
√ Not suitable for studying early stages of EOC |
√ Suitable for studying EOC dissemination |
√ No primary tumor formation |
√ Ascites formation |
√ Not suitable for studying angiogenesis |
√ Suitable for immunological studies |
|
√ Low cost |
|
Orthotopic model |
|
√ Tumor microenvironment recapitulates physiological conditions |
√ Difficult to perform |
√ Suitable for studying all stages of disease |
√ Tumor growth measurement requires advanced methods |
√ Suitable for studying angiogenesis and tumor microenvironment |
√ High cost |
√ Suitable for immunological studies |
|
√ Good model to study disease progression |
|
√ Ascites formation |
|