Department of Colorectal Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
Carcinogenesis. 2020 Jul 14;41(7):993-1004. doi: 10.1093/carcin/bgz178.
Colon signet-ring cell carcinoma (SRCC) is a rare type of malignant dedifferentiated adenocarcinomas, and is associated with poor survival. However, an in-depth study of the biological features of SRCC is hindered by the lack of a reliable in vitro model of colon SRCC. Thus, the establishment of cell cultures from SRCC has become the most challenging task. Here, by harnessing the power of the organoid culture system, we describe the establishment of a human colon SRCC organoid line from a surgical sample from one patient with colon SRCC. The colon SRCC organoid line, YQ-173, was characterized for morphology, histology, ultrastructure and chromosome stability levels, showing that it resembles the histological and growth characteristics of the original tumor cells; xenografts were used to show that it also has a high tumor formation rate. RNA sequencing of YQ-173 compared with the normal tissue verified its mucinous nature. Capture-based targeted DNA sequencing combined with drug screening based on a bespoke 88 compound library identified that JAK2 might be a treatment target. An in vitro drug screening found that AT9283 and Pacritinib could be effective JAK2 inhibitors, which was consistent with the in vivo xenograft response. We report, for the first time, the establishment of an SRCC organoid line allowing in-depth study of SRCC biology, as well as a strategy to assess in vitro drug testing in a personalized fashion.
结肠印戒细胞癌(SRCC)是一种罕见的恶性去分化腺癌,与生存率差有关。然而,由于缺乏可靠的结肠 SRCC 体外模型,深入研究 SRCC 的生物学特征受到阻碍。因此,建立 SRCC 的细胞培养成为最具挑战性的任务。在这里,我们利用类器官培养系统的力量,描述了从一名结肠 SRCC 患者的手术样本中建立人结肠 SRCC 类器官系的过程。结肠 SRCC 类器官系 YQ-173 的特征为形态、组织学、超微结构和染色体稳定性水平,表明它类似于原始肿瘤细胞的组织学和生长特征;异种移植用于表明它也具有很高的肿瘤形成率。YQ-173 的 RNA 测序与正常组织相比证实了其黏液性质。基于定制的 88 种化合物库的捕获靶向 DNA 测序结合药物筛选,鉴定出 JAK2 可能是一个治疗靶点。体外药物筛选发现 AT9283 和 Pacritinib 可能是有效的 JAK2 抑制剂,这与体内异种移植反应一致。我们首次报告了建立 SRCC 类器官系,允许深入研究 SRCC 生物学,并提出了一种个性化评估体外药物测试的策略。