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MiR-429 suppresses the progression and metastasis of osteosarcoma by targeting ZEB1

MiR-429 functions as a tumor suppressor and has been observed in multiple types of cancer, but the effects and mechanisms of miR-429 in osteosarcoma are poorly understood. This study is performed to evaluate the functions of miR-429 in the progression of osteosarcoma. Firstly, the miR-429 expression...

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Autores principales: Deng, Yi, Luan, Fujun, Zeng, Li, Zhang, Yanjun, Ma, Kunlong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Leibniz Research Centre for Working Environment and Human Factors 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5491908/
https://www.ncbi.nlm.nih.gov/pubmed/28694763
http://dx.doi.org/10.17179/excli2017-258
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author Deng, Yi
Luan, Fujun
Zeng, Li
Zhang, Yanjun
Ma, Kunlong
author_facet Deng, Yi
Luan, Fujun
Zeng, Li
Zhang, Yanjun
Ma, Kunlong
author_sort Deng, Yi
collection PubMed
description MiR-429 functions as a tumor suppressor and has been observed in multiple types of cancer, but the effects and mechanisms of miR-429 in osteosarcoma are poorly understood. This study is performed to evaluate the functions of miR-429 in the progression of osteosarcoma. Firstly, the miR-429 expression in osteosarcoma tissues and osteosarcoma cells was detected using real time PCR, and the relationship between miR-429 expression and overall survival of osteosarcoma was analyzed. Secondly, the effects of miR-429 on the migration, invasion, proliferation and apoptosis of osteosarcoma cells were evaluated using transwell assay, wound-healing assay, CCK-8 assay and flow cytometry, respectively. Proteins related to epithelial-mesenchymal transition (EMT), E-cadherin, Vimentin, N-cadherin and Snail, were also detected using Western blot. Finally, the target gene of miR-429 in osteosarcoma was predicted and verified using dual luciferase assay and the expression correlation between them was analyzed using Pearson's correlation. MiR-429 was down-regulated in osteosarcoma tissues and osteosarcoma cells; the expression level of miR-429 was associated with the prognosis of osteosarcoma. High level of miR-429 in osteosarcoma cells significantly suppressed the migration, invasion and proliferation of cells but induced cells apoptosis. Furthermore, high level of miR-429 in osteosarcoma cells obviously increased the expression of E-cadherin protein but decreased the expression of Vimentin, N-Cadherin and Snail proteins. EMT inducer ZEB1 was the target gene of miR-429 and the expression of ZEB1 was negatively related to the miR-429 expression in osteosarcoma. In conclusion, miR-429 may functions as a tumor suppressor and be down-regulated in osteosarcoma. MiR-429 may suppress the progression and metastasis of osteosarcoma by down-regulating the ZEB1 expression.
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spelling pubmed-54919082017-07-10 MiR-429 suppresses the progression and metastasis of osteosarcoma by targeting ZEB1 Deng, Yi Luan, Fujun Zeng, Li Zhang, Yanjun Ma, Kunlong EXCLI J Original Article MiR-429 functions as a tumor suppressor and has been observed in multiple types of cancer, but the effects and mechanisms of miR-429 in osteosarcoma are poorly understood. This study is performed to evaluate the functions of miR-429 in the progression of osteosarcoma. Firstly, the miR-429 expression in osteosarcoma tissues and osteosarcoma cells was detected using real time PCR, and the relationship between miR-429 expression and overall survival of osteosarcoma was analyzed. Secondly, the effects of miR-429 on the migration, invasion, proliferation and apoptosis of osteosarcoma cells were evaluated using transwell assay, wound-healing assay, CCK-8 assay and flow cytometry, respectively. Proteins related to epithelial-mesenchymal transition (EMT), E-cadherin, Vimentin, N-cadherin and Snail, were also detected using Western blot. Finally, the target gene of miR-429 in osteosarcoma was predicted and verified using dual luciferase assay and the expression correlation between them was analyzed using Pearson's correlation. MiR-429 was down-regulated in osteosarcoma tissues and osteosarcoma cells; the expression level of miR-429 was associated with the prognosis of osteosarcoma. High level of miR-429 in osteosarcoma cells significantly suppressed the migration, invasion and proliferation of cells but induced cells apoptosis. Furthermore, high level of miR-429 in osteosarcoma cells obviously increased the expression of E-cadherin protein but decreased the expression of Vimentin, N-Cadherin and Snail proteins. EMT inducer ZEB1 was the target gene of miR-429 and the expression of ZEB1 was negatively related to the miR-429 expression in osteosarcoma. In conclusion, miR-429 may functions as a tumor suppressor and be down-regulated in osteosarcoma. MiR-429 may suppress the progression and metastasis of osteosarcoma by down-regulating the ZEB1 expression. Leibniz Research Centre for Working Environment and Human Factors 2017-05-05 /pmc/articles/PMC5491908/ /pubmed/28694763 http://dx.doi.org/10.17179/excli2017-258 Text en Copyright © 2017 Deng et al. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (http://creativecommons.org/licenses/by/4.0/) You are free to copy, distribute and transmit the work, provided the original author and source are credited.
spellingShingle Original Article
Deng, Yi
Luan, Fujun
Zeng, Li
Zhang, Yanjun
Ma, Kunlong
MiR-429 suppresses the progression and metastasis of osteosarcoma by targeting ZEB1
title MiR-429 suppresses the progression and metastasis of osteosarcoma by targeting ZEB1
title_full MiR-429 suppresses the progression and metastasis of osteosarcoma by targeting ZEB1
title_fullStr MiR-429 suppresses the progression and metastasis of osteosarcoma by targeting ZEB1
title_full_unstemmed MiR-429 suppresses the progression and metastasis of osteosarcoma by targeting ZEB1
title_short MiR-429 suppresses the progression and metastasis of osteosarcoma by targeting ZEB1
title_sort mir-429 suppresses the progression and metastasis of osteosarcoma by targeting zeb1
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5491908/
https://www.ncbi.nlm.nih.gov/pubmed/28694763
http://dx.doi.org/10.17179/excli2017-258
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