miR-493-5p downregulation has emerged as a critical player in cancer progression yet, the underlying mechanisms of miR-493-5p expression pattern and its function in prostate cancer remains to be elucidated. Here, we illustrate that miR-493-5p is frequently downregulated in prostate cancer, at least partially due to altered DNA methylation. miR-493-5p functions as a tumor suppressor in prostate cancer cells. c-Met, CREB1 and EGFR are downstream target genes of miR-493-5p. miR-493-5p inhibits EMT via AKT/GSK-3β/Snail signaling in prostate cancer. Taken together, our study identified c-Met, CREB1, EGFR and miR-493-5p establish a regulatory loop in prostate cancer, which could prove useful in the development of effective and therapies against prostate cancer.
c-Met, CREB1 and EGFR are involved in miR-493-5p inhibition of EMT via AKT/GSK-3β/Snail signaling in prostate cancer.
c-Met、CREB1 和 EGFR 参与 miR-493-5p 通过 AKT/GSK-3β/Snail 信号通路抑制前列腺癌中的 EMT
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| 期刊: | Oncotarget | 影响因子: | 0.000 |
| 时间: | 2017 | 起止号: | 2017 Jul 19; 8(47):82303-82313 |
| doi: | 10.18632/oncotarget.19398 | 靶点: | EGFR |
| 研究方向: | 信号转导 | 疾病类型: | 前列腺癌 |
| 信号通路: | PI3K/Akt | ||
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