Figures & data
Figure 1. The lncRNA CRNDE expression was up-regulated in PC. RT-PCR analysis was performed to measure the expression of lncRNA CRNDE in PC tissues (a) and cells (b).*p < 0.05, **p < 0.01, ***p < 0.001. Each cell experiment was repeated for 3 times
![Figure 1. The lncRNA CRNDE expression was up-regulated in PC. RT-PCR analysis was performed to measure the expression of lncRNA CRNDE in PC tissues (a) and cells (b).*p < 0.05, **p < 0.01, ***p < 0.001. Each cell experiment was repeated for 3 times](/cms/asset/5b05665f-3034-4fa0-a19d-7afc089bc313/kbie_a_1935402_f0001_b.gif)
Figure 2. miR-146a-5p is a target of lncRNA CRNDE. (a) The predicted lncRNA CRNDE binding site in the miR-146a-5p 3ʹ-UTR . (b) Relative luciferase activity of cells after co-transfection with wild type (WT) or mutant (Mut) lncRNA CRNDE 3′-UTR reporter genes and miR-146a-5p mimics. (d) miR-146a-5p was up-regulated in PC tissues. (D) miR-146a-5p was up-regulated in all 4 PC cells in comparison with the RWPE-1 cells. **p < 0.01, ***p < 0.001. Each cell experiment was repeated for 3 times
![Figure 2. miR-146a-5p is a target of lncRNA CRNDE. (a) The predicted lncRNA CRNDE binding site in the miR-146a-5p 3ʹ-UTR . (b) Relative luciferase activity of cells after co-transfection with wild type (WT) or mutant (Mut) lncRNA CRNDE 3′-UTR reporter genes and miR-146a-5p mimics. (d) miR-146a-5p was up-regulated in PC tissues. (D) miR-146a-5p was up-regulated in all 4 PC cells in comparison with the RWPE-1 cells. **p < 0.01, ***p < 0.001. Each cell experiment was repeated for 3 times](/cms/asset/f71b9f86-726b-43a8-8344-ea4749db9a71/kbie_a_1935402_f0002_oc.jpg)
Figure 3. SiRNA and inhibitor down-regulated the expressions of CRNDE and miR-146a-5p. (a) The expression of CRNDE was detected by qRT-PCR after siRNA 1# and siRNA 2# transfection. (b) The expression of miR-146a-5p was measured by qRT-PCR after inhibitor transfection. ***p < 0.001. Each cell experiment was repeated for 3 times
![Figure 3. SiRNA and inhibitor down-regulated the expressions of CRNDE and miR-146a-5p. (a) The expression of CRNDE was detected by qRT-PCR after siRNA 1# and siRNA 2# transfection. (b) The expression of miR-146a-5p was measured by qRT-PCR after inhibitor transfection. ***p < 0.001. Each cell experiment was repeated for 3 times](/cms/asset/1d366592-0964-4d77-9681-4e92ad74c627/kbie_a_1935402_f0003_b.gif)
Figure 4. Knockdown of miR-146a-5p reversed the effects of si-CRNDE on the proliferation of PC. CCK-8(a) and colony formation (b) assays were used to detect the proliferation of PC3 cell lines. *p < 0.05, ***p < 0.001. Each experiment was repeated for 3 times
![Figure 4. Knockdown of miR-146a-5p reversed the effects of si-CRNDE on the proliferation of PC. CCK-8(a) and colony formation (b) assays were used to detect the proliferation of PC3 cell lines. *p < 0.05, ***p < 0.001. Each experiment was repeated for 3 times](/cms/asset/fbd20c0e-7965-490f-95a2-ce52ec039460/kbie_a_1935402_f0004_oc.jpg)
Figure 5. Knockdown of miR-146a-5p reversed the effect of si-CRNDE on the apoptosis rates of PC. (a-b) Flow cytometry assay was performed to determine the apoptosis rates of PC. **p < 0.01, ***p < 0.001. Each experiment was repeated for 3 times
![Figure 5. Knockdown of miR-146a-5p reversed the effect of si-CRNDE on the apoptosis rates of PC. (a-b) Flow cytometry assay was performed to determine the apoptosis rates of PC. **p < 0.01, ***p < 0.001. Each experiment was repeated for 3 times](/cms/asset/fafee6dd-70ae-44be-9202-31ec8da89a93/kbie_a_1935402_f0005_oc.jpg)
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.