A novel human colon signet-ring cell carcinoma organoid line: establishment, characterization and application

Author:

Li Yaqi12,Wang Renjie12,Huang Dan23,Ma Xiaoji12,Mo Shaobo12,Guo Qiang4,Fu Guoxiang4,Li Yuanchuang4,Xu Xiaoya4,Hu Xiang12,Zhou Yi4,Deng Yun5,Zhang Long16,Chen Honghong4,Gao Jianjun4,Zhang Zhen5,Cai Sanjun12,Hua Guoqiang46,Peng Junjie12

Affiliation:

1. Department of Colorectal Surgery, Fudan University Shanghai Cancer Center, Shanghai, China

2. Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, China

3. Department of Pathology, Fudan University Shanghai Cancer Center, Shanghai, China

4. Institute of Radiation Medicine, Fudan University, Shanghai 200032, China

5. Department of Radiation Oncology, Fudan University Shanghai Cancer Center, Shanghai, China

6. Cancer Institute, Shanghai Cancer Center, Fudan University, Shanghai, China

Abstract

Abstract 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.

Funder

National Natural Science Foundation of China

Science and Technology Commission of Shanghai Municipality

Shanghai Sailing Program

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,General Medicine

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