Establishment of a metastatic patient-derived xenograft model of breast carcinoma

In this study, we investigated the development and application of patient-derived xenograft (PDX) models for metastatic breast carcinoma. Orthotopic PDX models were established from tumor tissue of invasive ductal breast carcinoma patients without prior neoadjuvant therapy. Following successful tumor engraftment in immunodeficient NOD SCID gamma (NSG) mice, primary tumors were surgically excised using a procedure simulating radical mastectomy, enabling extended post-operative survival for the development of eventual metastases. Tumor growth, the presence of lung metastases, along with their histopathological features and immunohistochemical profiles, were evaluated. Three stable and transplantable PDX models were successfully established. Spontaneous lung metastases developed in one model following surgical resection, and this metastatic capability was preserved across multiple in vivo passages. Despite the successful engraftment, significant discrepancies were observed between the immunohistochemical characteristics of the original patient tumors and their corresponding PDXs, particularly in hormone receptor status and Ki-67 proliferation marker expression. These findings highlight the challenges of maintaining molecular fidelity in traditional PDX models.

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Publication Details

Journal
Neoplasma
Published
2025-11-14
DOI
https://doi.org/10.4149/neo_2025_250627n283
Primary Topic
Cancer Research and Treatments
Type
article
Field-Weighted Citation Impact
0.00

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article

Establishment of a metastatic patient-derived xenograft model of breast carcinoma

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Neoplasma
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Establishment of a metastatic patient-derived xenograft model of breast carcinoma

Daniel Dyttert, Martin Boháč, Michal Mego, Monika Buríková, Eva Sedláčková, Lenka Trnkova, Andrea Čumová, Marián Karaba, Marina Cihova, Štefan Durdík, Melissa Tran, Nina Novotna
article en

Abstract

In this study, we investigated the development and application of patient-derived xenograft (PDX) models for metastatic breast carcinoma. Orthotopic PDX models were established from tumor tissue of invasive ductal breast carcinoma patients without prior neoadjuvant therapy. Following successful tumor engraftment in immunodeficient NOD SCID gamma (NSG) mice, primary tumors were surgically excised using a procedure simulating radical mastectomy, enabling extended post-operative survival for the development of eventual metastases. Tumor growth, the presence of lung metastases, along with their histopathological features and immunohistochemical profiles, were evaluated. Three stable and transplantable PDX models were successfully established. Spontaneous lung metastases developed in one model following surgical resection, and this metastatic capability was preserved across multiple in vivo passages. Despite the successful engraftment, significant discrepancies were observed between the immunohistochemical characteristics of the original patient tumors and their corresponding PDXs, particularly in hormone receptor status and Ki-67 proliferation marker expression. These findings highlight the challenges of maintaining molecular fidelity in traditional PDX models.

NeoplasmaVol. 72(05)
Cancer Research Institute of the Slovak Academy of Sciences (SK), Biomedical Research Center of the Slovak Academy of Sciences (SK), Comenius University Bratislava (SK)
Vedecká Grantová Agentúra MŠVVaŠ SR a SAV, European Regional Development Fund
Openalex Percentile: Top 64%
Cancer Research and Treatments
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