Mouse Models for Head and Neck Squamous Cell Carcinoma
Issued Date
2024-01-01
Resource Type
ISSN
00220345
eISSN
15440591
Scopus ID
2-s2.0-85192848938
Journal Title
Journal of Dental Research
Rights Holder(s)
SCOPUS
Bibliographic Citation
Journal of Dental Research (2024)
Suggested Citation
Zhou J., Liu C., Amornphimoltham P., Cheong S.C., Gutkind J.S., Chen Q., Wang Z. Mouse Models for Head and Neck Squamous Cell Carcinoma. Journal of Dental Research (2024). doi:10.1177/00220345241240997 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/98400
Title
Mouse Models for Head and Neck Squamous Cell Carcinoma
Corresponding Author(s)
Other Contributor(s)
Abstract
The prognosis and survival rate of head and neck squamous cell carcinoma (HNSCC) have remained unchanged for years, and the pathogenesis of HNSCC is still not fully understood, necessitating further research. An ideal animal model that accurately replicates the complex microenvironment of HNSCC is urgently needed. Among all the animal models for preclinical cancer research, tumor-bearing mouse models are the best known and widely used due to their high similarity to humans. Currently, mouse models for HNSCC can be broadly categorized into chemical-induced models, genetically engineered mouse models (GEMMs), and transplanted mouse models, each with its distinct advantages and limitations. In chemical-induced models, the carcinogen spontaneously initiates tumor formation through a multistep process. The resemblance of this model to human carcinogenesis renders it an ideal preclinical platform for studying HNSCC initiation and progression from precancerous lesions. The major drawback is that these models are time-consuming and, like human cancer, unpredictable in terms of timing, location, and number of lesions. GEMMs involve transgenic and knockout mice with gene modifications, leading to malignant transformation within a tumor microenvironment that recapitulates tumorigenesis in vivo, including their interaction with the immune system. However, most HNSCC GEMMs exhibit low tumor incidence and limited prognostic significance when translated to clinical studies. Transplanted mouse models are the most widely used in cancer research due to their consistency, availability, and efficiency. Based on the donor and recipient species matching, transplanted mouse models can be divided into xenografts and syngeneic models. In the latter, transplanted cells and host are from the same strain, making syngeneic models relevant to study functional immune system. In this review, we provide a comprehensive summary of the characteristics, establishment methods, and potential applications of these different HNSCC mouse models, aiming to assist researchers in choosing suitable animal models for their research.