| Literature DB >> 35820346 |
Michihisa Kono1, Shin Saito2, Ann Marie Egloff3, Clint T Allen4, Ravindra Uppaluri5.
Abstract
Preclinical models of cancer have long been paramount to understanding tumor development and advancing the treatment of cancer. Creating preclinical models that mimic the complexity and heterogeneity of human tumors is a key challenge in the advancement of cancer therapy. About ten years ago, we created the mouse oral carcinoma (MOC) cell line models that were derived from 7, 12-dimethylbenz(a) anthracene (DMBA)-induced mouse oral squamous cell cancers. This model has been used in numerous investigations, including studies on tumor biology and therapeutics. We have seen remarkable progress in cancer immunology in recent years, and these cell lines, which are syngeneic to C57BL/6 background, have also been used to study the anti-tumor immune response. Herein, we aim to review the MOC model from its development and characterization to its use in non-immunological and immunological preclinical head and neck squamous cell carcinoma (HNSCC) studies. Integrating and refining these MOC model studies and extending findings to other systems will provide crucial insights for translational approaches aimed at improving head and neck cancer treatment.Entities:
Keywords: Carcinogen-induced cancer; Immunocompetent mouse models; Oral squamous cell carcinoma
Mesh:
Year: 2022 PMID: 35820346 PMCID: PMC9364442 DOI: 10.1016/j.oraloncology.2022.106012
Source DB: PubMed Journal: Oral Oncol ISSN: 1368-8375 Impact factor: 5.972