The microRNA-218~Survivin axis regulates migration, invasion, and lymph node metastasis in cervical cancer
| dc.contributor.author | Kogo, Ryunosuke | |
| dc.contributor.author | How, Christine | |
| dc.contributor.author | Chaudary, Naz | |
| dc.contributor.author | Bruce, Jeff | |
| dc.contributor.author | Shi, Wei | |
| dc.contributor.author | Hill, Richard P. | |
| dc.contributor.author | Zahedi, Payam | |
| dc.contributor.author | Yip, Kenneth W. | |
| dc.contributor.author | Liu, Fei-Fei | |
| dc.date.accessioned | 2023-01-18T18:19:57Z | |
| dc.date.available | 2023-01-18T18:19:57Z | |
| dc.date.issued | 2014-12-25 | |
| dc.description.abstract | Cervical cancer is the third most common cancer in women worldwide. In the present study, global microRNA profiling for 79 cervical cancer patient samples led to the identification of miR-218 down-regulation in cervical cancer tissues compared to normal cervical tissues. Lower miR-218 expression was associated significantly with worse overall survival (OS), disease-free survival (DFS), and pelvic/aortic lymph node recurrence. In vitro, miR-218 over-expression decreased clonogenicity, migration, and invasion. Survivin (BIRC5) was subsequently identified as an important cervical cancer target of miR-218 using in silico prediction, mRNA profiling, and quantitative real-time PCR (qRT-PCR). Concordant with miR-218 over-expression, survivin knockdown by siRNA decreased clonogenicity, migration, and invasion. YM155, a small molecule survivin inhibitor, significantly suppressed tumor growth and lymph node metastasis in vivo. Our findings demonstrate that the miR-218~survivin axis inhibits cervical cancer progression by regulating clonogenicity, migration, and invasion, and suggest that the inhibition of survivin could be a potential therapeutic strategy to improve outcome in this disease. | en_US |
| dc.identifier.citation | Kogo, R., How, C., Chaudary, N., Bruce, J., Shi, W., Hill, R. P., Zahedi, P., Yip, K. W., & Liu, F. F. (2015). The microRNA-218~Survivin axis regulates migration, invasion, and lymph node metastasis in cervical cancer. Oncotarget, 6(2), 1090–1100. https://doi.org/10.18632/oncotarget.2836 | en_US |
| dc.identifier.other | DOI: 10.18632/oncotarget.2836 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14041/5644 | |
| dc.language.iso | en_US | en_US |
| dc.publisher | Oncotarget | en_US |
| dc.rights | Attribution-NonCommercial-NoDerivs 3.0 United States | * |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/us/ | * |
| dc.subject | miR-218 | en_US |
| dc.subject | Survivin | en_US |
| dc.subject | Cervical Cancer | en_US |
| dc.subject | Migration | en_US |
| dc.subject | Invasion | en_US |
| dc.title | The microRNA-218~Survivin axis regulates migration, invasion, and lymph node metastasis in cervical cancer | en_US |
| dc.type | Article | en_US |
