Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States; Department of Otolaryngology - Head and Neck Surgery, Asahikawa Medical University, Asahikawa, Japan.
Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, United States; Department of Otolaryngology - Head and Neck Surgery, Keio University School of Medicine, Tokyo, Japan.
Oral Oncol. 2022 Sep;132:106012. doi: 10.1016/j.oraloncology.2022.106012. Epub 2022 Jul 9.
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.
长期以来,癌症的临床前模型对于理解肿瘤的发展和推进癌症治疗至关重要。创建能够模拟人类肿瘤复杂性和异质性的临床前模型是癌症治疗进展的关键挑战。大约十年前,我们创建了源自 7,12-二甲基苯并蒽(DMBA)诱导的小鼠口腔鳞状细胞癌的小鼠口腔癌(MOC)细胞系模型。该模型已被广泛应用于许多研究,包括肿瘤生物学和治疗学的研究。近年来,我们在癌症免疫学方面取得了显著进展,这些与 C57BL/6 背景同源的细胞系也被用于研究抗肿瘤免疫反应。在此,我们旨在回顾 MOC 模型从其发展和表征到在非免疫学和免疫学头颈部鳞状细胞癌(HNSCC)临床前研究中的应用。整合和完善这些 MOC 模型研究,并将研究结果扩展到其他系统,将为旨在改善头颈部癌症治疗的转化方法提供关键见解。