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. 2023 May 19;14:2861. doi: 10.1038/s41467-023-38581-8

Fig. 8. Overexpression of ADAR1 and hyper-editing/overexpression of SCD1 are strongly associated with the pathogenesis of gastric cancer.

Fig. 8

a Kaplan-Meier overall survival plot comparing gastric cancer patients with high ADAR1 and high SCD1 proteomic expression versus low ADAR1 and low SCD1 proteomic expression. All gastric cancer patients were treated with a combination of 5FU and platinum-based chemotherapy in an adjuvant clinical setting. b Expression level of ADAR1 and SCD1 and its correlation with percent tumor remaining. All gastric cancer patients were treated with a combination of 5FU and platinum-based chemotherapy in a neoadjuvant clinical setting. c Pearson correlation analysis of ADAR1 mRNA expression with SCD1 editing in TCGA-STAD. d ADAR1 mRNA expression in responder versus non-responder to chemotherapy treatment in TCGA-STAD. e ADAR1 mRNA/SCD1 editing signature in responder versus non-responder to chemotherapy in TCGA-STAD. f Kaplan-Meier overall survival plot comparing patients with ADAR1 mRNA/SCD1 editing signature >0 with ADAR1 mRNA/SCD1 editing signature <0. For panels (d-f), only GC patients of intestinal subtype treated with 5FU or platinum-based chemotherapy were considered. Significance were calculated by (a, f) log-rank test; (b, d, e) unpaired two-tailed student t-test; (c) two-tailed Pearson correlation analysis. All data was presented as mean ± standard deviation. Source data are provided as a Source Data file.