TY - JOUR
T1 - Establishment of a Large-Scale PDX Library of Head and Neck Cancers for Functional Precision Oncology
AU - Yanagi, Hisano
AU - Kuki, Tomoki
AU - Takimoto, Tetsuya
AU - Takabayashi, Miki
AU - Yamada, Seiji
AU - Yagi, Chikako
AU - Kiryu, Yoshitake
AU - Kurimoto, Maki
AU - Ishikawa, Miho
AU - Yoshida, Arisa
AU - Mizutani, Yasuyoshi
AU - Enomoto, Atsushi
AU - Suzuki, Motoshi
AU - Kawada, Kenji
AU - Kato, Hisayuki
AU - Tateya, Ichiro
AU - Saya, Hideyuki
AU - Watanabe, Takashi
N1 - Publisher Copyright:
© 2026 The Author(s). Cancer Medicine published by John Wiley & Sons Ltd.
PY - 2026/2
Y1 - 2026/2
N2 - Background: Precision oncology leverages the molecular and genetic characteristics of tumors to enable accurate diagnosis and effective treatment selection. However, recent clinical trials have highlighted the limitations of current approaches and underscored the need to integrate static molecular profiling with functional analyses using patient-derived xenograft (PDX) models—particularly for cancers such as head and neck cancer (HNC), where driver mutations are rare and prognosis remains poor. Methods: Here, we aimed to establish a large-scale PDX library for HNC, termed the Fujita Xenograft Library (FXeL), annotated with detailed clinical information. Since 2022, tumor specimens from over 100 surgical cases at Fujita Health University Hospital have been transplanted into immunodeficient mice, resulting in the successful establishment of 62 PDX models. Results: Advanced clinical stage was significantly associated with successful engraftment, and serial passaging led to progressively accelerated tumor growth. Comparative analyses of genomic profiles between patient tumors and PDXs demonstrated that major cancer-related mutations were largely preserved in PDXs, while clonal selection and evolution occurred during engraftment. Histopathological features, including keratinization and nuclear atypia, were retained, whereas stromal components such as cancer-associated fibroblasts exhibited compositional shifts. Furthermore, drug sensitivity assays revealed that PDX responses to cisplatin (CDDP) closely mirrored the clinical outcomes of the corresponding patients. Conclusions: The FXeL represents a robust and scalable platform for investigating HNC biology and therapeutic response. Despite limitations such as stromal remodeling and the absence of an immune microenvironment, these models provide valuable translational insights and support the advancement of functional precision oncology.
AB - Background: Precision oncology leverages the molecular and genetic characteristics of tumors to enable accurate diagnosis and effective treatment selection. However, recent clinical trials have highlighted the limitations of current approaches and underscored the need to integrate static molecular profiling with functional analyses using patient-derived xenograft (PDX) models—particularly for cancers such as head and neck cancer (HNC), where driver mutations are rare and prognosis remains poor. Methods: Here, we aimed to establish a large-scale PDX library for HNC, termed the Fujita Xenograft Library (FXeL), annotated with detailed clinical information. Since 2022, tumor specimens from over 100 surgical cases at Fujita Health University Hospital have been transplanted into immunodeficient mice, resulting in the successful establishment of 62 PDX models. Results: Advanced clinical stage was significantly associated with successful engraftment, and serial passaging led to progressively accelerated tumor growth. Comparative analyses of genomic profiles between patient tumors and PDXs demonstrated that major cancer-related mutations were largely preserved in PDXs, while clonal selection and evolution occurred during engraftment. Histopathological features, including keratinization and nuclear atypia, were retained, whereas stromal components such as cancer-associated fibroblasts exhibited compositional shifts. Furthermore, drug sensitivity assays revealed that PDX responses to cisplatin (CDDP) closely mirrored the clinical outcomes of the corresponding patients. Conclusions: The FXeL represents a robust and scalable platform for investigating HNC biology and therapeutic response. Despite limitations such as stromal remodeling and the absence of an immune microenvironment, these models provide valuable translational insights and support the advancement of functional precision oncology.
KW - chemotherapy sensitivity
KW - functional precision oncology
KW - head and neck cancer
KW - patient-derived xenograft (PDX) library
KW - preclinical mouse model
UR - https://www.scopus.com/pages/publications/105030438570
UR - https://www.scopus.com/pages/publications/105030438570#tab=citedBy
U2 - 10.1002/cam4.71521
DO - 10.1002/cam4.71521
M3 - Article
C2 - 41709080
AN - SCOPUS:105030438570
SN - 2045-7634
VL - 15
JO - Cancer Medicine
JF - Cancer Medicine
IS - 2
M1 - e71521
ER -