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Updated: May 4, 2026

Generation and Culturing of High-Grade Serous Ovarian Cancer Patient-Derived Organoids
Published on: January 6, 2023
Patient-derived xenograft models to improve targeted therapy in epithelial ovarian cancer treatment
Clare L Scott1, Marc A Becker2, Paul Haluska2
1Walter and Eliza Hall Institute of Medical Research, Royal Melbourne Hospital and The Royal Women's Hospital , Melbourne, VIC , Australia.
Abstract:
Despite increasing evidence that precision therapy targeted to the molecular drivers of a cancer has the potential to improve clinical outcomes, high-grade epithelial ovarian cancer (OC) patients are currently treated without consideration of molecular phenotype, and predictive biomarkers that could better inform treatment remain unknown. Delivery of precision therapy requires improved integration of laboratory-based models and cutting-edge clinical research, with pre-clinical models predicting patient subsets that will benefit from a particular targeted therapeutic. Patient-derived xenografts (PDXs) are renewable tumor models engrafted in mice, generated from fresh human tumors without prior in vitro exposure. PDX models allow an invaluable assessment of tumor evolution and adaptive response to therapy. PDX models have been applied to pre-clinical drug testing and biomarker identification in a number of cancers including ovarian, pancreatic, breast, and prostate cancers. These models have been shown to be biologically stable and accurately reflect the patient tumor with regards to histopathology, gene expression, genetic mutations, and therapeutic response. However, pre-clinical analyses of molecularly annotated PDX models derived from high-grade serous ovarian cancer (HG-SOC) remain limited. In vivo response to conventional and/or targeted therapeutics has only been described for very small numbers of individual HG-SOC PDX in conjunction with sparse molecular annotation and patient outcome data. Recently, two consecutive panels of epithelial OC PDX correlate in vivo platinum response with molecular aberrations and source patient clinical outcomes. These studies underpin the value of PDX models to better direct chemotherapy and predict response to targeted therapy. Tumor heterogeneity, before and following treatment, as well as the importance of multiple molecular aberrations per individual tumor underscore some of the important issues addressed in PDX models.
Insights
Precision therapy for ovarian cancer (OC) lacks molecular guidance. Patient-derived xenografts (PDXs) offer a promising preclinical model to identify biomarkers and predict treatment response in high-grade serous ovarian cancer.
Area of Science:
- Oncology
- Translational Research
- Genomics
Background:
- High-grade epithelial ovarian cancer (OC) treatment lacks molecular phenotype consideration.
- Predictive biomarkers for OC treatment remain largely unknown.
- Precision therapy requires robust preclinical models to identify patient subsets benefiting from targeted agents.
Purpose of the Study:
- To evaluate the utility of patient-derived xenografts (PDXs) in high-grade serous ovarian cancer (HG-SOC) for preclinical drug testing and biomarker discovery.
- To correlate in vivo therapeutic response in HG-SOC PDX models with molecular aberrations and patient outcomes.
Main Methods:
- Generation and characterization of HG-SOC patient-derived xenografts (PDXs).
- Preclinical testing of conventional and targeted therapeutics in PDX models.
- Molecular annotation of PDX models, including gene expression and mutations.
- Correlation of in vivo drug response with molecular data and source patient clinical outcomes.
Main Results:
- PDX models accurately reflect the histopathology, gene expression, and mutations of the original patient tumors.
- Recent studies demonstrate a correlation between platinum response in OC PDXs and specific molecular aberrations.
- PDX models facilitate the assessment of tumor evolution and adaptive responses to therapy, addressing tumor heterogeneity.
Conclusions:
- Patient-derived xenografts (PDXs) are valuable preclinical models for high-grade serous ovarian cancer (HG-SOC).
- PDX models can guide chemotherapy selection and predict response to targeted therapies by integrating molecular data and patient outcomes.
- Further research utilizing molecularly annotated PDX models is crucial for advancing precision medicine in ovarian cancer.

