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Molecular mechanisms governing microRNA-125a expression in human hepatocellular carcinoma cells

MicroRNA-125a-5p (miR-125a) is a vertebrate homolog of lin-4, the first discovered microRNA, and plays a fundamental role in embryo development by downregulating Lin-28 protein. MiR-125a is also expressed in differentiated cells where it generally acts as an antiproliferative factor by targeting mem...

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Autores principales: Potenza, Nicoletta, Panella, Marta, Castiello, Filomena, Mosca, Nicola, Amendola, Elena, Russo, Aniello
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587745/
https://www.ncbi.nlm.nih.gov/pubmed/28878257
http://dx.doi.org/10.1038/s41598-017-11418-3
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author Potenza, Nicoletta
Panella, Marta
Castiello, Filomena
Mosca, Nicola
Amendola, Elena
Russo, Aniello
author_facet Potenza, Nicoletta
Panella, Marta
Castiello, Filomena
Mosca, Nicola
Amendola, Elena
Russo, Aniello
author_sort Potenza, Nicoletta
collection PubMed
description MicroRNA-125a-5p (miR-125a) is a vertebrate homolog of lin-4, the first discovered microRNA, and plays a fundamental role in embryo development by downregulating Lin-28 protein. MiR-125a is also expressed in differentiated cells where it generally acts as an antiproliferative factor by targeting membrane receptors or intracellular transductors of mitogenic signals. MiR-125a expression is downregulated in several tumors, including hepatocellular carcinoma (HCC) where it targets sirtuin-7, matrix metalloproteinase-11, VEGF-A, Zbtb7a, and c-Raf. In this study, we have isolated the transcription promoter of human miR-125a and characterized its activity in HCC cells. It is a TATA-less Pol II promoter provided with an initiator element and a downstream promoter element, located 3939 bp upstream the genomic sequence of the miRNA. The activity of the promoter is increased by the transcription factor NF-kB, a master regulator of inflammatory response, and miR-125a itself was found to strengthen this activation through inhibition of TNFAIP3, a negative regulator of NF-kB. This finding contributes to explain the increased levels of miR-125a observed in the liver of patients with chronic hepatitis B.
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spelling pubmed-55877452017-09-13 Molecular mechanisms governing microRNA-125a expression in human hepatocellular carcinoma cells Potenza, Nicoletta Panella, Marta Castiello, Filomena Mosca, Nicola Amendola, Elena Russo, Aniello Sci Rep Article MicroRNA-125a-5p (miR-125a) is a vertebrate homolog of lin-4, the first discovered microRNA, and plays a fundamental role in embryo development by downregulating Lin-28 protein. MiR-125a is also expressed in differentiated cells where it generally acts as an antiproliferative factor by targeting membrane receptors or intracellular transductors of mitogenic signals. MiR-125a expression is downregulated in several tumors, including hepatocellular carcinoma (HCC) where it targets sirtuin-7, matrix metalloproteinase-11, VEGF-A, Zbtb7a, and c-Raf. In this study, we have isolated the transcription promoter of human miR-125a and characterized its activity in HCC cells. It is a TATA-less Pol II promoter provided with an initiator element and a downstream promoter element, located 3939 bp upstream the genomic sequence of the miRNA. The activity of the promoter is increased by the transcription factor NF-kB, a master regulator of inflammatory response, and miR-125a itself was found to strengthen this activation through inhibition of TNFAIP3, a negative regulator of NF-kB. This finding contributes to explain the increased levels of miR-125a observed in the liver of patients with chronic hepatitis B. Nature Publishing Group UK 2017-09-06 /pmc/articles/PMC5587745/ /pubmed/28878257 http://dx.doi.org/10.1038/s41598-017-11418-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Potenza, Nicoletta
Panella, Marta
Castiello, Filomena
Mosca, Nicola
Amendola, Elena
Russo, Aniello
Molecular mechanisms governing microRNA-125a expression in human hepatocellular carcinoma cells
title Molecular mechanisms governing microRNA-125a expression in human hepatocellular carcinoma cells
title_full Molecular mechanisms governing microRNA-125a expression in human hepatocellular carcinoma cells
title_fullStr Molecular mechanisms governing microRNA-125a expression in human hepatocellular carcinoma cells
title_full_unstemmed Molecular mechanisms governing microRNA-125a expression in human hepatocellular carcinoma cells
title_short Molecular mechanisms governing microRNA-125a expression in human hepatocellular carcinoma cells
title_sort molecular mechanisms governing microrna-125a expression in human hepatocellular carcinoma cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5587745/
https://www.ncbi.nlm.nih.gov/pubmed/28878257
http://dx.doi.org/10.1038/s41598-017-11418-3
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