Prognostic significance of frequent CLDN18-ARHGAP26/6 fusion in gastric signet-ring cell cancer

Yang Shu(Sichuan University), Weihan Zhang(Central South University), Qianqian Hou(Sichuan University), Lin-Yong Zhao(Sichuan University), Shouyue Zhang(Sichuan University), Jiankang Zhou(Sichuan University), Xiao-Hai Song(Sichuan University), Yan Zhang(Sichuan University), Dan Jiang(Sichuan University), Xin‐Zu Chen(Sichuan University), Peiqi Wang(Albert Einstein College of Medicine), Xuyang Xia(Sichuan University), Fei Liao(Sichuan University), Dandan Yin(Sichuan University), Xiao‐Long Chen(Sichuan University), Xueyan Zhou(Sichuan University), Duyu Zhang(Sichuan University), Senlin Yin(Sichuan University), Kun Yang(Sichuan University), Jianping Liu(Sichuan University), Leilei Fu(Sichuan University), Lan Zhang(Sichuan University), Yuelan Wang(Sichuan University), Jun‐Long Zhang(Sichuan University), Yunfei An(Sichuan University), Hua Cheng, Bin Zheng, Hongye Sun, Yinglan Zhao(Sichuan University), Yongsheng Wang(Sichuan University), Dan Xie(Sichuan University), Liang Ouyang(Sichuan University), Ping Wang(Albert Einstein College of Medicine), Yaoguang Zhang(Central South University), Meng Qiu(Sichuan University), Xianghui Fu(Sichuan University), Lunzhi Dai(Sichuan University), Gu He(Sichuan University), Hanshuo Yang(Sichuan University), Wei Cheng(Sichuan University), Li Yang(Sichuan University), Bo Liu(Sichuan University), Weimin Li(Sichuan University), Biao Dong(Sichuan University), Zong‐Guang Zhou(Sichuan University), Yuquan Wei(Sichuan University), Yong Peng(Sichuan University), Heng Xu(Sichuan University), Jian‐Kun Hu(Sichuan University)
Nature Communications
June 18, 2018
Cited by 142Open Access
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Abstract

Signet-ring cell carcinoma (SRCC) has specific epidemiology and oncogenesis in gastric cancer, however, with no systematical investigation for prognostic genomic features. Here we report a systematic investigation conducted in 1868 Chinese gastric cancer patients indicating that signet-ring cells content was related to multiple clinical characteristics and treatment outcomes. We thus perform whole-genome sequencing on 32 pairs of SRC samples, and identify frequent CLDN18-ARHGAP26/6 fusion (25%). With 797 additional patients for validation, prevalence of CLDN18-ARHGAP26/6 fusion is noticed to be associated with signet-ring cell content, age at diagnosis, female/male ratio, and TNM stage. Importantly, patients with CLDN18-ARHGAP26/6 fusion have worse survival outcomes, and get no benefit from oxaliplatin/fluoropyrimidines-based chemotherapy, which is consistent with the fact of chemo-drug resistance acquired in CLDN18-ARHGAP26 introduced cell lines. Overall, this study provides insights into the clinical and genomic features of SRCC, and highlights the importance of frequent CLDN18-ARHGAP26/6 fusions in chemotherapy response for SRCC.


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