Nature Communications · 2018 · 143 citations · 41 references
MedicineGeneticsOncologyCancer GeneticsMolecular OncologyOncogenesCancer GenomicsCancer Molecular PathologyGastric CancerGene Fusions In CancerMalignant NeoplasmsNext-generation Sequencing In OncologyAnticancer ChemotherapyGastric Cancer GeneticsGenomic BiomarkersNext-generation Sequencing AnalysisPrognostic VariablesSignet Ring Cell CarcinomaSignet Ring Cell MorphologyTnm Staging System
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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