941
Views
12
CrossRef citations to date
0
Altmetric
Research paper

microRNA-877-5p exerts tumor-suppressive functions in prostate cancer through repressing transcription of forkhead box M1

, , , & ORCID Icon
Pages 9094-9102 | Received 26 Aug 2021, Accepted 02 Oct 2021, Published online: 27 Oct 2021

Figures & data

Table 1. Relationship between miR-877-5p expression and clinical parameters of patients with PCa

Table 2. Multivariate Cox analysis of clinical characteristics in relation to overall survival

Figure 1. miR-877-5p is downregulated in prostate cancer. (a). Relative expression of miR-877-5p in prostate cancer tissue and normal tissue samples (n = 101). (b). miR-877-5p expression in prostate cancer cell lines and normal prostatic epithelial cell RWPE-1. n = 4. *P < 0.05, ***P < 0.001

Figure 1. miR-877-5p is downregulated in prostate cancer. (a). Relative expression of miR-877-5p in prostate cancer tissue and normal tissue samples (n = 101). (b). miR-877-5p expression in prostate cancer cell lines and normal prostatic epithelial cell RWPE-1. n = 4. *P < 0.05, ***P < 0.001

Figure 2. The 5-year survival rate of prostate cancer patients with different miR-877-5p expression levels (log-rank test P = 0.003)

Figure 2. The 5-year survival rate of prostate cancer patients with different miR-877-5p expression levels (log-rank test P = 0.003)

Figure 3. Proliferation of DU-145 and LNCap cells was suppressed after the upregulation of miR-877-5p compared to untreated cells. DU-145 and LNCap cells were transfected with mimic NC or miR-877-5p mimic. (a) and (b) miR-877-5p expression was determined in DU-145 and LNCap cells by qRT-PCR. n = 5. (c) and (d) Proliferative capacity of DU-145 and LNCap cells were measured by CCK-8. n = 3. (e) and (f) Migratory ability of DU-145 and LNCap cells were measured by transwell assay; n = 5. (g) and (h) Invasive ability of DU-145 and LNCap cells were detected using transwell assay. n = 5. *P < 0.05, ***P < 0.001

Figure 3. Proliferation of DU-145 and LNCap cells was suppressed after the upregulation of miR-877-5p compared to untreated cells. DU-145 and LNCap cells were transfected with mimic NC or miR-877-5p mimic. (a) and (b) miR-877-5p expression was determined in DU-145 and LNCap cells by qRT-PCR. n = 5. (c) and (d) Proliferative capacity of DU-145 and LNCap cells were measured by CCK-8. n = 3. (e) and (f) Migratory ability of DU-145 and LNCap cells were measured by transwell assay; n = 5. (g) and (h) Invasive ability of DU-145 and LNCap cells were detected using transwell assay. n = 5. *P < 0.05, ***P < 0.001

Figure 4. miR-877-5p interacted with FOXM1. (a) The binding site between FOXM1 and miR-877-5p is shown. (b) The correlation between miRNA-143-3p and miR-877-5p expression in prostate cancer tissues was analyzed by Spearman correlation analysis. n = 101. (c) Expression of FOXM1 was measured using qRT-PCR in DU-145 cells that were transfected with mimic NC or miR-877-5p mimic separately; n = 5. (d) Luciferase activity was examined in DU-145 cell cotransfected with miR-877-5p mimic, mimic NC, miR-877-5p inhibitor, or inhibitor NC and WT-FOXM1 or MUT-FOXM1. n = 3. **P < 0.01, ***P < 0.001

Figure 4. miR-877-5p interacted with FOXM1. (a) The binding site between FOXM1 and miR-877-5p is shown. (b) The correlation between miRNA-143-3p and miR-877-5p expression in prostate cancer tissues was analyzed by Spearman correlation analysis. n = 101. (c) Expression of FOXM1 was measured using qRT-PCR in DU-145 cells that were transfected with mimic NC or miR-877-5p mimic separately; n = 5. (d) Luciferase activity was examined in DU-145 cell cotransfected with miR-877-5p mimic, mimic NC, miR-877-5p inhibitor, or inhibitor NC and WT-FOXM1 or MUT-FOXM1. n = 3. **P < 0.01, ***P < 0.001