ページを選択

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.  

当社の前臨床サービスについて、さらに詳しい情報をお探しですか?

✓  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.  

研究に最適なツールを手に入れよう

当社の腫瘍学プラットフォームを探索・比較し、研究ニーズに最適なモデルを特定してください。

腫瘍学リーフレットダウンロード

Patient-derived Xenograft (PDX) Mouse Models Sample Data

Key Patient-derived Xenograft (PDX) Mouse Models Readouts

InnoSer推奨の読み取り値


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 

    あなたの研究を支える人々

    セリーヌ・エレンス博士、免疫学研究 ディレクター

    当社の免疫腫瘍学研究責任者セリーヌ・エレンス率いる専門家チームが、適切なツールの選択と最適な試験設計の構築を支援します。当該分野への深い理解に基づき、リード化合物の前臨床試験を厳選することで、貴社の医薬品開発を加速するソリューションを提供します。

    ヤニック・ファントン博士、最高科学責任者

    イノサーの最高科学責任者として、ヤニックはイノサーにおける全ての顧客調査を担当し、科学的・技術的な調整業務を統括している。

    腫瘍学理事会メンバー

    エスター・ヴォルフス教授博士

    イノサーの科学諮問委員会のメンバーであるウルフス博士は、幹細胞治療の第一人者である。現在ハッセルト大学の教授を務める エスターは 抗がん治療における幹細胞の利用と、シャルコー・マリー・トゥース病1A型の研究モデルとしての幹細胞活用に取り組んでいる。

    マリエ・スリンガーランド

    医学博士、博士(医学)マリエ・スリンガーランド

    イノサーの科学諮問委員会のメンバーであるライデン大学医療センターのスリンガーランド博士は、消化器癌および頭頸部癌における臨床試験、特に腫瘍内免疫パラメータに焦点を当てている。

    よくあるご質問

    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.

    研究に最適なツールを手に入れよう

    当社の腫瘍学プラットフォームを探索・比較し、研究ニーズに最適なモデルを特定してください。

    腫瘍学リーフレットダウンロード

    好奇心を持ち続けよう:さらに探求できる記事

    Personalized Lymphoma CDX mouse models for preclinical oncology

    Personalized Lymphoma CDX mouse models for preclinical oncology

    In recent studies, we established and validated two new human lymphoma cell‑line–derived xenograft (CDX) models, generated from the OCI‑Ly19 (diffuse large B‑cell lymphoma, DLBCL) and REC‑1 (mantle cell lymphoma) cell lines. These models were developed in strategic...

    免疫腫瘍学研究におけるマルチプレックスサイトカインおよび免疫細胞プロファイリング

    免疫腫瘍学研究におけるマルチプレックスサイトカインおよび免疫細胞プロファイリング

    メソスケール・ディスカバリー(MSD)プラットフォームは、高感度かつ多重のサイトカインプロファイリング分析システムであり、ごく微量のサンプル(わずか1μL)から複数の標的サイトカイン、ケモカイン、抗体、成長因子を同時に定量することが可能です。これにより...

    膵臓癌患者由来異種移植モデル

    膵臓癌患者由来異種移植モデル

    先月11月は膵臓がん啓発月間でした。これは最も攻撃的で致死率の高いがん種の一つがもたらす課題に焦点を当てる時期です。膵臓がんは欧州で診断される全がんの約3%を占め、膵臓...

    AAALAC認定

    InnoSerはAAALAC認証を取得し、責任ある動物ケアと利用への取り組みを実証しています。AAALAC Internationalは、自主的な認証および評価プログラムを通じて科学における動物の適切な扱いを推進する非営利組織です。InnoSerのオランダおよびベルギー施設は、それぞれ2016年および2020年よりAAALAC認証を取得しています。AAALAC認証プログラムの詳細はこちらをご覧ください。

    AAALACロゴ

    動物福祉

    3R原則は、政策や規制の変更から新技術・手法の開発と普及に至るまで、あらゆる分野に影響を及ぼします。このためInnoSerは、これらのプロセスに対する継続的な取り組みと監視を実施しています。当社が実践する手順は、動物実験の代替・削減・改善を最大限に実現し、研究および医薬品開発におけるこれらの原則への取り組みを促進します。

    義務なし – 今すぐ始めよう

    info@innoserlaboratories.com