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Regulation of IL-8 gene expression in gliomas by microRNA miR-93

BACKGROUND: Different strategies have been proposed to target neoangiogenesis in gliomas, besides those targeting Vascular Endothelial Growth Factor (VEGF). The chemokine Interleukin-8 (IL-8) has been shown to possess both tumorigenic and proangiogenic properties. Although different pathways of indu...

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Autores principales: Fabbri, Enrica, Brognara, Eleonora, Montagner, Giulia, Ghimenton, Claudio, Eccher, Albino, Cantù, Cinzia, Khalil, Susanna, Bezzerri, Valentino, Provezza, Lisa, Bianchi, Nicoletta, Finotti, Alessia, Borgatti, Monica, Moretto, Giuseppe, Chilosi, Marco, Cabrini, Giulio, Gambari, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4598972/
https://www.ncbi.nlm.nih.gov/pubmed/26449498
http://dx.doi.org/10.1186/s12885-015-1659-1
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author Fabbri, Enrica
Brognara, Eleonora
Montagner, Giulia
Ghimenton, Claudio
Eccher, Albino
Cantù, Cinzia
Khalil, Susanna
Bezzerri, Valentino
Provezza, Lisa
Bianchi, Nicoletta
Finotti, Alessia
Borgatti, Monica
Moretto, Giuseppe
Chilosi, Marco
Cabrini, Giulio
Gambari, Roberto
author_facet Fabbri, Enrica
Brognara, Eleonora
Montagner, Giulia
Ghimenton, Claudio
Eccher, Albino
Cantù, Cinzia
Khalil, Susanna
Bezzerri, Valentino
Provezza, Lisa
Bianchi, Nicoletta
Finotti, Alessia
Borgatti, Monica
Moretto, Giuseppe
Chilosi, Marco
Cabrini, Giulio
Gambari, Roberto
author_sort Fabbri, Enrica
collection PubMed
description BACKGROUND: Different strategies have been proposed to target neoangiogenesis in gliomas, besides those targeting Vascular Endothelial Growth Factor (VEGF). The chemokine Interleukin-8 (IL-8) has been shown to possess both tumorigenic and proangiogenic properties. Although different pathways of induction of IL-8 gene expression have been already elucidated, few data are available on its post-transcriptional regulation in gliomas. METHODS: Here we investigated the role of the microRNA miR-93 on the expression levels of IL-8 and other pro-inflammatory genes by RT-qPCR and Bio-Plex analysis. We used different disease model systems, including clinical samples from glioma patients and two glioma cell lines, U251 and T98G. RESULTS: IL-8 and VEGF transcripts are highly expressed in low and high grade gliomas in respect to reference healthy brain; miR-93 expression is also increased and inversely correlated with transcription of IL-8 and VEGF genes. Computational analysis showed the presence of miR-93 consensus sequences in the 3′UTR region of both VEGF and IL-8 mRNAs, predicting possible interaction with miR-93 and suggesting a potential regulatory role of this microRNA. In vitro transfection with pre-miR-93 and antagomiR-93 inversely modulated VEGF and IL-8 gene expression and protein release when the glioma cell line U251 was considered. Similar data were obtained on IL-8 gene regulation in the other glioma cell line analyzed, T98G. The effect of pre-miR-93 and antagomiR-93 in U251 cells has been extended to the secretion of a panel of cytokines, chemokines and growth factors, which consolidated the concept of a role of miR-93 in IL-8 and VEGF gene expression and evidenced a potential regulatory role also for MCP-1 and PDGF (also involved in angiogenesis). CONCLUSION: In conclusion, our results suggest an increasing role of miR-93 in regulating the level of expression of several genes involved in the angiogenesis of gliomas. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-015-1659-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-45989722015-10-09 Regulation of IL-8 gene expression in gliomas by microRNA miR-93 Fabbri, Enrica Brognara, Eleonora Montagner, Giulia Ghimenton, Claudio Eccher, Albino Cantù, Cinzia Khalil, Susanna Bezzerri, Valentino Provezza, Lisa Bianchi, Nicoletta Finotti, Alessia Borgatti, Monica Moretto, Giuseppe Chilosi, Marco Cabrini, Giulio Gambari, Roberto BMC Cancer Research Article BACKGROUND: Different strategies have been proposed to target neoangiogenesis in gliomas, besides those targeting Vascular Endothelial Growth Factor (VEGF). The chemokine Interleukin-8 (IL-8) has been shown to possess both tumorigenic and proangiogenic properties. Although different pathways of induction of IL-8 gene expression have been already elucidated, few data are available on its post-transcriptional regulation in gliomas. METHODS: Here we investigated the role of the microRNA miR-93 on the expression levels of IL-8 and other pro-inflammatory genes by RT-qPCR and Bio-Plex analysis. We used different disease model systems, including clinical samples from glioma patients and two glioma cell lines, U251 and T98G. RESULTS: IL-8 and VEGF transcripts are highly expressed in low and high grade gliomas in respect to reference healthy brain; miR-93 expression is also increased and inversely correlated with transcription of IL-8 and VEGF genes. Computational analysis showed the presence of miR-93 consensus sequences in the 3′UTR region of both VEGF and IL-8 mRNAs, predicting possible interaction with miR-93 and suggesting a potential regulatory role of this microRNA. In vitro transfection with pre-miR-93 and antagomiR-93 inversely modulated VEGF and IL-8 gene expression and protein release when the glioma cell line U251 was considered. Similar data were obtained on IL-8 gene regulation in the other glioma cell line analyzed, T98G. The effect of pre-miR-93 and antagomiR-93 in U251 cells has been extended to the secretion of a panel of cytokines, chemokines and growth factors, which consolidated the concept of a role of miR-93 in IL-8 and VEGF gene expression and evidenced a potential regulatory role also for MCP-1 and PDGF (also involved in angiogenesis). CONCLUSION: In conclusion, our results suggest an increasing role of miR-93 in regulating the level of expression of several genes involved in the angiogenesis of gliomas. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-015-1659-1) contains supplementary material, which is available to authorized users. BioMed Central 2015-10-08 /pmc/articles/PMC4598972/ /pubmed/26449498 http://dx.doi.org/10.1186/s12885-015-1659-1 Text en © Fabbri et al. 2015 Open AccessThis 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Fabbri, Enrica
Brognara, Eleonora
Montagner, Giulia
Ghimenton, Claudio
Eccher, Albino
Cantù, Cinzia
Khalil, Susanna
Bezzerri, Valentino
Provezza, Lisa
Bianchi, Nicoletta
Finotti, Alessia
Borgatti, Monica
Moretto, Giuseppe
Chilosi, Marco
Cabrini, Giulio
Gambari, Roberto
Regulation of IL-8 gene expression in gliomas by microRNA miR-93
title Regulation of IL-8 gene expression in gliomas by microRNA miR-93
title_full Regulation of IL-8 gene expression in gliomas by microRNA miR-93
title_fullStr Regulation of IL-8 gene expression in gliomas by microRNA miR-93
title_full_unstemmed Regulation of IL-8 gene expression in gliomas by microRNA miR-93
title_short Regulation of IL-8 gene expression in gliomas by microRNA miR-93
title_sort regulation of il-8 gene expression in gliomas by microrna mir-93
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4598972/
https://www.ncbi.nlm.nih.gov/pubmed/26449498
http://dx.doi.org/10.1186/s12885-015-1659-1
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