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Oncology CRO services – Patient-derived Xenograft (PDX) Mouse Models 

Recapitulate the tumor and patient heterogeneity and response to treatment using patient-derived xenograft (PDX) mouse models     

Home » Oncology CRO Services » Patient-derived Xenograft (PDX) Mouse Models

InnoSer’s Patient-derived Xenograft (PDX) Mouse Models Services

Patient-derived xenograft (PDX) mouse models are established from resected tumor samples obtained from oncologic patients that are implanted and grown in immunodeficient mice. However, to fully recapitulate the intricacies between the immune system and the tumor microenvironment, humanized mouse models are recommended instead of immunodeficient mice. Patient-derived xenograft (PDX) mouse models represent the most clinically relevant and predictive tool in your drug development journey, recapitulating the tumor and patient heterogeneity, gene expression, and response to treatment.  

Therefore, experts from InnoSer’s immuno-oncology team recommend the use of PDX mouse models whenever you have carried out initial in vivo studies using cell line-derived (CDX) mouse models and wish to obtain more clinically relevant results. Accordingly, patient-derived xenografts are suitable for evaluating a range of therapies ranging from immunotherapy, antibody, antibody-drug conjugate, and gene therapies to small molecules (cytotoxic drugs). PDX models provide you with a highly predictive in vivo model for therapeutic efficacy evaluation.

Compared to other preclinical in vivo models, patient-derived xenograft models represent more robust models, requiring longer study timelines and the inclusion of different patient samples to capture your compound’s efficacy on patient heterogeneity.  

Looking for more details about our preclinical services?

✓  Well-characterised parental samples (histopathology, hot spot analyses, mutational burden, treatment history, response to treatment). 

✓ On-request PDX expansion services.

PDX

Developing new, safe, and efficacious anticancer therapies is an extremely intricate process. As a preclinical oncology contract research organization (CRO), InnoSer partners with you to help you navigate the complexities of this research area.

Scientists at InnoSer collaborate with you to develop the most optimal study design to help answer your research questions most cost-effectively. With flexible and fast study start times you can perform your research at an accelerated pace. By outsourcing your preclinical oncology studies to InnoSer, you gain access to our in vitro and in vivo oncology drug development portfolio.  

Unlock the Right Tools for Your Research.

Explore and compare our oncology platforms to identify the perfect model for your study needs.

oncology leaflet download

Patient-derived Xenograft (PDX) Mouse Models Sample Data

Key Patient-derived Xenograft (PDX) Mouse Models Readouts

InnoSer's Recommended Readouts


Test the efficacy of your treatments using PDX mouse models with the following readouts: 

 

  • Response to treatment (tumor growth kinetics, body weight, clinical signs, survival analyses) 
  • Histopathology 

    The People Behind Your Research

    Céline Erens, PhD, Immunology Study Director

    An expert team led by our immuno-oncology study director, Céline Erens helps you choose the right tools and set up optimal study designs. Curating the preclinical testing of your lead compounds with a deep understanding of the field is your solution to accelerating your drug development.

    Yanick Fanton, PhD, Chief Scientific Officer

    As Chief Science Officer at InnoSer, Yanick is responsible for all customer studies at InnoSer and takes care of the scientific and technical coordination.

    Oncology Board Members

    Prof. Dr. Esther Wolfs

    A member of InnoSer’s Scientific Advisory Board, Dr. Wolfs is a leading researcher in stem cell therapy. Currently a professor at the University of Hasselt, Ester uses stem cells in anticancer therapy and as a model to study Charcot-Marie-Tooth disease type 1A.

    Marije Slingerland

    MD, PhD Marije Slingerland

    A member of InnoSer’s Scientific Advisory Board, Dr. Slingerland from Leiden University Medical Center focuses on clinical trials in gastrointestinal cancer and in head and neck cancer, particularly on intratumoral immune parameters.

    Frequently Asked Questions

    What is the difference between PDX and CDX mouse models?

    Cell line-derived xenograft (CDX) mouse models are established by injecting immunodeficient or humanized mice with immortalised human cancer cell lines in contrast to patient-derived xenograft (PDX) models which are established by injecting the primary tumor material into mice. While CDX mouse models are useful for high-throughput and cost-effective preclinical studies, they lack the tumor heterogeneity of primary tumor, which are preserved in PDX mouse models. Preserving both the tumor and stromal cell heterogeneity, PDX mouse models are better suited for studying tumor biology and treatment responses that closely reflect patient tumors.

    Choose the most appropriate model for your research in consultation with our study experts.

    Are patient derived xenograft (PDX) mouse models accurate representations of primary tumors?
    PDX models are widely regarded as more accurate representations of primary human tumors compared to cell line-derived models. This is due to their ability to retain the tumor heterogeneity and genomic landscape of the original patient tumor, including its stromal and tumor cell components which are critical for understanding the tumor behavior in response to new therapies. However, the immunodeficient subcutaneous murine microenvironment differs significantly from the human host environment, which can limit the translational relevance in immune-oncology research. This limitation may be addressed by working with humanized mouse models. Moreover, long-term propagation of PDX tumors may result in genetic and phenotypic drift, potentially compromising their fidelity to the original tumor.InnoSer addresses these challenges by working with PDX lines that have not undergone extensive propagation steps, ensuring they remain representative of the patient tumor.
    What is the most suitable mouse and genetic backgrounds for PDX studies?
    PDX studies require immunodeficient mice to enable the engraftment and growth of human cancer cells. At InnoSer, we have extensive experience with several immunodeficient strains, including:
    • Nude mice: The immunocompromised nude mice represent the ideal recipient mouse strain due to no rejection responses. The absence of fur in nude mice may also additionally make it easier to identify subcutaneous tumors.
    • NSG (NOD scid gamma) mice: The highly immunodeficient NSG mice are suitable for engraftment of human tumors as well as the establishment of human immunity following hematopoietic stem cell transplantation.
    • BRGSF mice: Compared to nude and NSG mice, BRGSF mice represent the most defective immunodeficient strain, suitable for xenografting of human tumors or transplantation of the human immune system.
    When should I use humanized mice for PDX applications?
    Normally, PDX is implanted into immunodeficient mice to prevent immune reaction. However, this does not allow studying of the therapeutic response in a mouse model with an immune system. The engraftment of patient-derived tumor fragments into humanized mice allows for the presence of human tumor tissue, stromal elements, and a complete human immune system in one model.

    Unlock the Right Tools for Your Research.

    Explore and compare our oncology platforms to identify the perfect model for your study needs.

    oncology leaflet download

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    InnoSer has earned the AAALAC accreditation, demonstrating our commitment to responsible animal care and use. AAALAC International is a nonprofit organization that promotes the humane treatment of animals in science through voluntary accreditation and assessment programs. Our accreditation is valid for three years, incl. 2023. Read more about the AAALAC accreditation programme here.

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    Animal Welfare

    The 3Rs impact everything from policy and regulatory change to the development and uptake of new technologies and approaches. This is why InnoSer has ongoing commitment and monitoring of these processes. The steps we practice maximize our ability to replace, reduce and refine animal involvement and facilitate our commitment to these principles when it comes to research and drug development.

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