| miR-21 |
promotes tumor invasiveness and induces castration-resistance phenotype. |
[76–77] |
| miR-221/miR-222 |
enhance cell proliferation, invasion, cell survival, increase clonogenicity and enhance tumorigenicity in vivo. |
[78–80] |
| miR-141 |
is important in androgen-dependent and in metastatic castration-resistant. |
[81–82] |
| miR-375 |
is important for an early diagnosis. |
[83–84] |
| miR-18a |
promotes cancer progression. |
[85] |
| miR-4534 |
induces pro-cancerous characteristics in non-cancer cell line. |
[87] |
| miR-650 |
suppresses the cellular stress response 1 (CSR1) expression. |
[88] |
| miR-32 |
inhibits apoptosis and enhances proliferation. |
[89] |
| miR-106/miR-25 |
facilitate tumor progression. |
[90] |
| miR-125b |
enhances cell proliferation and inhibits apoptosis. |
[91] |
