Department of Digestive Surgery, Breast and Thyroid Surgery, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan; Department of Biomedical Sciences, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Division of Gastroenterology, Department of Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania; University of Pennsylvania Abramson Cancer Center, Philadelphia, Pennsylvania.
Cell Mol Gastroenterol Hepatol. 2018 Sep 14;7(1):73-91. doi: 10.1016/j.jcmgh.2018.09.003. eCollection 2019.
BACKGROUND & AIMS: Oropharyngeal and esophageal squamous cell carcinomas, especially the latter, are a lethal disease, featuring intratumoral cancer cell heterogeneity and therapy resistance. To facilitate cancer therapy in personalized medicine, three-dimensional (3D) organoids may be useful for functional characterization of cancer cells . We investigated the feasibility and the utility of patient-derived 3D organoids of esophageal and oropharyngeal squamous cell carcinomas.
We generated 3D organoids from paired biopsies representing tumors and adjacent normal mucosa from therapy-naïve patients and cell lines. We evaluated growth and structures of 3D organoids treated with 5-fluorouracil .
Tumor-derived 3D organoids were grown successfully from 15 out of 21 patients (71.4%) and passaged with recapitulation of the histopathology of the original tumors. Successful formation of tumor-derived 3D organoids was associated significantly with poor response to presurgical neoadjuvant chemotherapy or chemoradiation therapy in informative patients ( = 0.0357, progressive and stable diseases, n = 10 vs. partial response, n = 6). The 3D organoid formation capability and 5-fluorouracil resistance were accounted for by cancer cells with high CD44 expression and autophagy, respectively. Such cancer cells were found to be enriched in patient-derived 3D organoids surviving 5-fluorouracil treatment.
The single cell-based 3D organoid system may serve as a highly efficient platform to explore cancer therapeutics and therapy resistance mechanisms in conjunction with morphological and functional assays with implications for translation in personalized medicine.
口咽和食管鳞状细胞癌,尤其是后者,是一种致命的疾病,具有肿瘤内癌细胞异质性和治疗耐药性。为了促进个性化医学中的癌症治疗,三维(3D)类器官可能有助于癌症细胞的功能特征分析。我们研究了来自未经治疗的患者和细胞系的肿瘤和相邻正常黏膜的配对活检的食管和口咽鳞状细胞癌患者衍生的 3D 类器官的可行性和实用性。
我们从 21 名患者中的 15 名(71.4%)成功生成了肿瘤衍生的 3D 类器官,并进行了传代培养,以重现原始肿瘤的组织病理学特征。肿瘤衍生的 3D 类器官的成功形成与信息丰富的患者中术前新辅助化疗或放化疗的不良反应显著相关(=0.0357,进展和稳定疾病,n=10 与部分缓解,n=6)。3D 类器官形成能力和 5-氟尿嘧啶耐药性分别与高 CD44 表达和自噬的癌细胞有关。在 5-氟尿嘧啶治疗后存活的患者衍生的 3D 类器官中发现了这种富含癌细胞。
基于单细胞的 3D 类器官系统可能是一种高效的平台,可与形态学和功能测定相结合,探索癌症治疗和治疗耐药性机制,对个性化医学的转化具有重要意义。