Cargando…
miRNA-101 Targets TGF-βR1 to Retard the Progression of Oral Squamous Cell Carcinoma
Despite the considerable knowledge on the involvement of microRNA-101 (miR-101) in the evolution of oral squamous cell carcinoma (OSCC), the underlying mechanisms remain obscure. In this study, miR-101 expression was markedly downregulated in the OSCC cell lines and tissues. Cell counting kit-8 (CCK...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cognizant Communication Corporation
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851522/ https://www.ncbi.nlm.nih.gov/pubmed/31831099 http://dx.doi.org/10.3727/096504019X15761480623959 |
_version_ | 1783645648319414272 |
---|---|
author | Wang, Yong Jia, Rui-Zhi Diao, Shu He, Jun Jia, Li |
author_facet | Wang, Yong Jia, Rui-Zhi Diao, Shu He, Jun Jia, Li |
author_sort | Wang, Yong |
collection | PubMed |
description | Despite the considerable knowledge on the involvement of microRNA-101 (miR-101) in the evolution of oral squamous cell carcinoma (OSCC), the underlying mechanisms remain obscure. In this study, miR-101 expression was markedly downregulated in the OSCC cell lines and tissues. Cell counting kit-8 (CCK-8), ethynyl deoxyuridine (EdU), and colony formation assays showed that miR-101 inhibited the proliferation of OSCC cells. Flow cytometry and caspase 3 activity assays indicated that miR-101 induced OSCC cell apoptosis. Transwell assays demonstrated that this miRNA also repressed OSCC cell migration and invasion. Moreover, tube formation assay showed that miR-101 abated the proangiogenesis of OSCC cells. Dual-luciferase reporter assay confirmed that miR-101 directly targeted transforming growth factor-β receptor 1 (TGF-βR1) in OSCC. Ectopic expression of TGF-βR1 counteracted the effects of miR-101 on the OSCC cell characteristics. Thus, miR-101 significantly abolished the proliferation, motility, and proangiogenesis of OSCC cells and induced their apoptosis by targeting TGF-βR1. These results imply the potential application of miR-101 in OSCC treatment. |
format | Online Article Text |
id | pubmed-7851522 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cognizant Communication Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-78515222021-02-16 miRNA-101 Targets TGF-βR1 to Retard the Progression of Oral Squamous Cell Carcinoma Wang, Yong Jia, Rui-Zhi Diao, Shu He, Jun Jia, Li Oncol Res Article Despite the considerable knowledge on the involvement of microRNA-101 (miR-101) in the evolution of oral squamous cell carcinoma (OSCC), the underlying mechanisms remain obscure. In this study, miR-101 expression was markedly downregulated in the OSCC cell lines and tissues. Cell counting kit-8 (CCK-8), ethynyl deoxyuridine (EdU), and colony formation assays showed that miR-101 inhibited the proliferation of OSCC cells. Flow cytometry and caspase 3 activity assays indicated that miR-101 induced OSCC cell apoptosis. Transwell assays demonstrated that this miRNA also repressed OSCC cell migration and invasion. Moreover, tube formation assay showed that miR-101 abated the proangiogenesis of OSCC cells. Dual-luciferase reporter assay confirmed that miR-101 directly targeted transforming growth factor-β receptor 1 (TGF-βR1) in OSCC. Ectopic expression of TGF-βR1 counteracted the effects of miR-101 on the OSCC cell characteristics. Thus, miR-101 significantly abolished the proliferation, motility, and proangiogenesis of OSCC cells and induced their apoptosis by targeting TGF-βR1. These results imply the potential application of miR-101 in OSCC treatment. Cognizant Communication Corporation 2020-03-27 /pmc/articles/PMC7851522/ /pubmed/31831099 http://dx.doi.org/10.3727/096504019X15761480623959 Text en Copyright © 2020 Cognizant, LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This article is licensed under a Creative Commons Attribution-NonCommercial NoDerivatives 4.0 International License. |
spellingShingle | Article Wang, Yong Jia, Rui-Zhi Diao, Shu He, Jun Jia, Li miRNA-101 Targets TGF-βR1 to Retard the Progression of Oral Squamous Cell Carcinoma |
title | miRNA-101 Targets TGF-βR1 to Retard the Progression of Oral Squamous Cell Carcinoma |
title_full | miRNA-101 Targets TGF-βR1 to Retard the Progression of Oral Squamous Cell Carcinoma |
title_fullStr | miRNA-101 Targets TGF-βR1 to Retard the Progression of Oral Squamous Cell Carcinoma |
title_full_unstemmed | miRNA-101 Targets TGF-βR1 to Retard the Progression of Oral Squamous Cell Carcinoma |
title_short | miRNA-101 Targets TGF-βR1 to Retard the Progression of Oral Squamous Cell Carcinoma |
title_sort | mirna-101 targets tgf-βr1 to retard the progression of oral squamous cell carcinoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7851522/ https://www.ncbi.nlm.nih.gov/pubmed/31831099 http://dx.doi.org/10.3727/096504019X15761480623959 |
work_keys_str_mv | AT wangyong mirna101targetstgfbr1toretardtheprogressionoforalsquamouscellcarcinoma AT jiaruizhi mirna101targetstgfbr1toretardtheprogressionoforalsquamouscellcarcinoma AT diaoshu mirna101targetstgfbr1toretardtheprogressionoforalsquamouscellcarcinoma AT hejun mirna101targetstgfbr1toretardtheprogressionoforalsquamouscellcarcinoma AT jiali mirna101targetstgfbr1toretardtheprogressionoforalsquamouscellcarcinoma |