Cargando…
Eupatilin Inhibits Renal Cancer Growth by Downregulating MicroRNA-21 through the Activation of YAP1
Renal cell carcinoma (RCC) is the second most common human urinary tumor. Eupatilin is the main active ingredient of the traditional Chinese medicine Artemisia asiatica. The effect of Eupatilin on RCC and the underlying mechanism remain unknown. Here, we investigated the anticancer effects and mecha...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6507163/ https://www.ncbi.nlm.nih.gov/pubmed/31179326 http://dx.doi.org/10.1155/2019/5016483 |
_version_ | 1783416974203682816 |
---|---|
author | Zhong, Weifeng Wu, Zhiming Chen, Nanhui Zhong, Kaihua Lin, Yifeng Jiang, Huiming Wan, Pei Lu, Shanming Yang, Lawei Liu, Siping |
author_facet | Zhong, Weifeng Wu, Zhiming Chen, Nanhui Zhong, Kaihua Lin, Yifeng Jiang, Huiming Wan, Pei Lu, Shanming Yang, Lawei Liu, Siping |
author_sort | Zhong, Weifeng |
collection | PubMed |
description | Renal cell carcinoma (RCC) is the second most common human urinary tumor. Eupatilin is the main active ingredient of the traditional Chinese medicine Artemisia asiatica. The effect of Eupatilin on RCC and the underlying mechanism remain unknown. Here, we investigated the anticancer effects and mechanisms of Eupatilin in RCC in vivo and in vitro, laying an experimental foundation for the clinical application of Eupatilin in the treatment of RCC. The results showed that Eupatilin significantly inhibited 786-O cell viability and migration and promoted apoptosis. Eupatilin inhibited the expression of miR-21 in 786-O cells, and overexpression of miR-21 suppressed the effect of Eupatilin on viability, apoptosis, and migration in 786-O cells. Eupatilin inhibited the growth of renal tumors in nude mice by downregulating miR-21. YAP1, which was identified as a target of miR-21, showed significantly lower expression in RCC tissues than in healthy tissues. miR-21 significantly inhibited YAP1 protein expression in 786-O cells and tumor tissues isolated from nude mice, and YAP1 attenuated the effect of miR-21 on the viability, apoptosis, and migration of 786-O cells. In conclusion, Eupatilin inhibited the expression of miR-21, which mediated the proapoptotic and antimigratory effects of Eupatilin by suppressing YAP1 in renal cancer cells. These results suggested that Eupatilin could be a potent agent for the treatment of RCC. |
format | Online Article Text |
id | pubmed-6507163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-65071632019-06-09 Eupatilin Inhibits Renal Cancer Growth by Downregulating MicroRNA-21 through the Activation of YAP1 Zhong, Weifeng Wu, Zhiming Chen, Nanhui Zhong, Kaihua Lin, Yifeng Jiang, Huiming Wan, Pei Lu, Shanming Yang, Lawei Liu, Siping Biomed Res Int Research Article Renal cell carcinoma (RCC) is the second most common human urinary tumor. Eupatilin is the main active ingredient of the traditional Chinese medicine Artemisia asiatica. The effect of Eupatilin on RCC and the underlying mechanism remain unknown. Here, we investigated the anticancer effects and mechanisms of Eupatilin in RCC in vivo and in vitro, laying an experimental foundation for the clinical application of Eupatilin in the treatment of RCC. The results showed that Eupatilin significantly inhibited 786-O cell viability and migration and promoted apoptosis. Eupatilin inhibited the expression of miR-21 in 786-O cells, and overexpression of miR-21 suppressed the effect of Eupatilin on viability, apoptosis, and migration in 786-O cells. Eupatilin inhibited the growth of renal tumors in nude mice by downregulating miR-21. YAP1, which was identified as a target of miR-21, showed significantly lower expression in RCC tissues than in healthy tissues. miR-21 significantly inhibited YAP1 protein expression in 786-O cells and tumor tissues isolated from nude mice, and YAP1 attenuated the effect of miR-21 on the viability, apoptosis, and migration of 786-O cells. In conclusion, Eupatilin inhibited the expression of miR-21, which mediated the proapoptotic and antimigratory effects of Eupatilin by suppressing YAP1 in renal cancer cells. These results suggested that Eupatilin could be a potent agent for the treatment of RCC. Hindawi 2019-04-24 /pmc/articles/PMC6507163/ /pubmed/31179326 http://dx.doi.org/10.1155/2019/5016483 Text en Copyright © 2019 Weifeng Zhong et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zhong, Weifeng Wu, Zhiming Chen, Nanhui Zhong, Kaihua Lin, Yifeng Jiang, Huiming Wan, Pei Lu, Shanming Yang, Lawei Liu, Siping Eupatilin Inhibits Renal Cancer Growth by Downregulating MicroRNA-21 through the Activation of YAP1 |
title | Eupatilin Inhibits Renal Cancer Growth by Downregulating MicroRNA-21 through the Activation of YAP1 |
title_full | Eupatilin Inhibits Renal Cancer Growth by Downregulating MicroRNA-21 through the Activation of YAP1 |
title_fullStr | Eupatilin Inhibits Renal Cancer Growth by Downregulating MicroRNA-21 through the Activation of YAP1 |
title_full_unstemmed | Eupatilin Inhibits Renal Cancer Growth by Downregulating MicroRNA-21 through the Activation of YAP1 |
title_short | Eupatilin Inhibits Renal Cancer Growth by Downregulating MicroRNA-21 through the Activation of YAP1 |
title_sort | eupatilin inhibits renal cancer growth by downregulating microrna-21 through the activation of yap1 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6507163/ https://www.ncbi.nlm.nih.gov/pubmed/31179326 http://dx.doi.org/10.1155/2019/5016483 |
work_keys_str_mv | AT zhongweifeng eupatilininhibitsrenalcancergrowthbydownregulatingmicrorna21throughtheactivationofyap1 AT wuzhiming eupatilininhibitsrenalcancergrowthbydownregulatingmicrorna21throughtheactivationofyap1 AT chennanhui eupatilininhibitsrenalcancergrowthbydownregulatingmicrorna21throughtheactivationofyap1 AT zhongkaihua eupatilininhibitsrenalcancergrowthbydownregulatingmicrorna21throughtheactivationofyap1 AT linyifeng eupatilininhibitsrenalcancergrowthbydownregulatingmicrorna21throughtheactivationofyap1 AT jianghuiming eupatilininhibitsrenalcancergrowthbydownregulatingmicrorna21throughtheactivationofyap1 AT wanpei eupatilininhibitsrenalcancergrowthbydownregulatingmicrorna21throughtheactivationofyap1 AT lushanming eupatilininhibitsrenalcancergrowthbydownregulatingmicrorna21throughtheactivationofyap1 AT yanglawei eupatilininhibitsrenalcancergrowthbydownregulatingmicrorna21throughtheactivationofyap1 AT liusiping eupatilininhibitsrenalcancergrowthbydownregulatingmicrorna21throughtheactivationofyap1 |