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MicroRNA-495 downregulates FOXC1 expression to suppress cell growth and migration in endometrial cancer

MicroRNAs (miRNAs) are a class of noncoding RNAs and function as key regulators of gene expression at the post-transcriptional level. In this study, we found that miR-495 reduces cell growth, induces apoptosis and suppresses the migration of endometrial cancer by directly inhibiting FOXC1 expression...

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Detalles Bibliográficos
Autores principales: Xu, Yan-Ying, Tian, Jing, Hao, Quan, Yin, Li-Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4841847/
https://www.ncbi.nlm.nih.gov/pubmed/26198045
http://dx.doi.org/10.1007/s13277-015-3686-6
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author Xu, Yan-Ying
Tian, Jing
Hao, Quan
Yin, Li-Rong
author_facet Xu, Yan-Ying
Tian, Jing
Hao, Quan
Yin, Li-Rong
author_sort Xu, Yan-Ying
collection PubMed
description MicroRNAs (miRNAs) are a class of noncoding RNAs and function as key regulators of gene expression at the post-transcriptional level. In this study, we found that miR-495 reduces cell growth, induces apoptosis and suppresses the migration of endometrial cancer by directly inhibiting FOXC1 expression. Further analysis revealed that FOXC1 promotes growth and migration and functions as an oncogene in vitro. FOXC1 overexpression reversed the cellular responses mediated by miR-495 in endometrial cancer cells. We also found that miR-495 suppresses the growth of endometrial cancer in vivo. Altogether, these results indicate that miR-495 acts as a tumour suppressor gene by targeting FOXC1 at the post-transcriptional level in endometrial cancer.
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spelling pubmed-48418472016-05-16 MicroRNA-495 downregulates FOXC1 expression to suppress cell growth and migration in endometrial cancer Xu, Yan-Ying Tian, Jing Hao, Quan Yin, Li-Rong Tumour Biol Research Article MicroRNAs (miRNAs) are a class of noncoding RNAs and function as key regulators of gene expression at the post-transcriptional level. In this study, we found that miR-495 reduces cell growth, induces apoptosis and suppresses the migration of endometrial cancer by directly inhibiting FOXC1 expression. Further analysis revealed that FOXC1 promotes growth and migration and functions as an oncogene in vitro. FOXC1 overexpression reversed the cellular responses mediated by miR-495 in endometrial cancer cells. We also found that miR-495 suppresses the growth of endometrial cancer in vivo. Altogether, these results indicate that miR-495 acts as a tumour suppressor gene by targeting FOXC1 at the post-transcriptional level in endometrial cancer. Springer Netherlands 2015-07-22 /pmc/articles/PMC4841847/ /pubmed/26198045 http://dx.doi.org/10.1007/s13277-015-3686-6 Text en © The Author(s) 2015 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research Article
Xu, Yan-Ying
Tian, Jing
Hao, Quan
Yin, Li-Rong
MicroRNA-495 downregulates FOXC1 expression to suppress cell growth and migration in endometrial cancer
title MicroRNA-495 downregulates FOXC1 expression to suppress cell growth and migration in endometrial cancer
title_full MicroRNA-495 downregulates FOXC1 expression to suppress cell growth and migration in endometrial cancer
title_fullStr MicroRNA-495 downregulates FOXC1 expression to suppress cell growth and migration in endometrial cancer
title_full_unstemmed MicroRNA-495 downregulates FOXC1 expression to suppress cell growth and migration in endometrial cancer
title_short MicroRNA-495 downregulates FOXC1 expression to suppress cell growth and migration in endometrial cancer
title_sort microrna-495 downregulates foxc1 expression to suppress cell growth and migration in endometrial cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4841847/
https://www.ncbi.nlm.nih.gov/pubmed/26198045
http://dx.doi.org/10.1007/s13277-015-3686-6
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