Loading...
Please wait, while we are loading the content...
Similar Documents
miR-27a-3p targeting RXRα promotes colorectal cancer progression by activating Wnt/β-catenin pathway
| Content Provider | Semantic Scholar |
|---|---|
| Author | Liang, Jiangtao Tang, Jianming Shi, Huijuan Zhen, Tiantian Duan, Jing Kang, Lili Zhang, Fenfen Dong, Yu Han, Anjia |
| Copyright Year | 2017 |
| Abstract | This study aimed to elucidate how miR-27a-3p modulates the Wnt/β-catenin signaling pathway to promote colorectal cancer (CRC) progression. Our results showed that the expression of miR-27a-3p was up-regulated in CRC and closely associated with histological differentiation, clinical stage, distant metastasis and CRC patients' survival. miR-27a-3p mimic suppressed apoptosis and promoted proliferation, migration, invasion of CRC cells in vitro and in vivo. Whereas miR-27a-3p inhibitor promoted apoptosis and suppressed proliferation, migration, invasion of CRC cells in vitro and in vivo. Furthermore, RXRα was the target gene of miR-27a-3p in CRC. miR-27a-3p expression negatively correlated with RXRα expression in CRC tissues. The underlining mechanism study showed that miR-27a-3p/RXRα/Wnt/β-catenin signaling pathway is involved in CRC progression. In conclusion, our findings first demonstrate that miR-27a-3p is a prognostic and/or potential therapeutic biomarker for CRC patients and RXRα as miR-27a-3p targeting gene plays an important role in activation of the Wnt/β-catenin pathway during CRC progression. |
| Starting Page | 82991 |
| Ending Page | 83008 |
| Page Count | 18 |
| File Format | PDF HTM / HTML |
| DOI | 10.18632/oncotarget.19635 |
| Alternate Webpage(s) | http://www.oncotarget.com/index.php?journal=oncotarget&op=download&page=article&path%5B%5D=19635&path%5B%5D=62727 |
| PubMed reference number | 28778091 |
| Alternate Webpage(s) | https://doi.org/10.18632/oncotarget.19635 |
| Journal | Medline |
| Volume Number | 8 |
| Journal | Oncotarget |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |