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. 2022 Apr 21;47(6):111. doi: 10.3892/or.2022.8322

Figure 3.

Figure 3.

Representative genes whose expression is potentially regulated by DEK. (A and B) FPKM values of representative DEGs that were significantly upregulated or downregulated in the siDEK condition in a human GC cell line AGS are shown as bar plots. Gray and purple bars show the FPKM values of the siCtrl- and siDEK-treated AGS cells, respectively. Bars and error bars represent means and SEMs, respectively. **P<0.01, ***P<0.001. (C and D) Relative expression levels of DEGs (% of GAPDH) in shRNA-infected cells in AGS and NUGC4 cell lines were validated by RT-qPCR assay, respectively. Statistical differences between groups (shScr and either shDEK_1 or shDEK_2) were tested using one-way ANOVA with Newman-Keuls multiple comparisons test, and P<0.05 was considered statistically significant. Bars and error bars represent the mean ± SD, respectively (n=3). **P<0.01, ***P<0.001. (E) Correlation of gene expression levels between DEK and CCDC80, PSAT1 and PSPH from public datasets are shown as dot plots. Each dot represents a single GC case. All the data were derived from the GEPIA2 database (http://gepia2.cancer-pku.cn/#correlation). (F) Kaplan-Meier curves of GC patients as stratified with high and low expression levels of CCDC80, PSAT1 and PSPH. All of the data were obtained from the GSE22377 (N=43) dataset. (http://kmplot.com/analysis/index.php?p=service&cancer=gastric). P-values were calculated by log-rank test. GC, gastric cancer; FPKM, fragments per kilobase of transcript per million fragments mapped; DEGs, differentially expressed genes; ACTA2, alpha smooth muscle actin; CXCL10, chemokine (C-X-C motif) ligand 10; HMOX1, heme oxygenase-1; SPRR2A, small proline-rich protein 2A; KIFC3, kinesin family member C3; OSBPL5, oxysterol binding protein like 5; CCDC80, coiled-coil domain containing 80; ASNS, asparagine synthetase; CHAC1, cation transport regulator 1; DDIT4, DNA damage-inducible transcript 4; ERRFI1, ERBB receptor feedback inhibitor 1; FAM3C, FAM3 metabolism regulating signaling molecule C; JDP2, Jun dimerization protein 2; RMRP, RNA component of mitochondrial RNA processing; PSAT1, phosphoserine aminotransferase 1; PSPH, phosphoserine phosphatase.