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miR-21 coordinates tumor growth and modulates KRIT1 levels
miR-21 is overexpressed in tumors and it displays oncogenic activity. Here, we show that expression of miR-21 in primary tumors anticorrelates with KRIT1/CCM1, an interacting partner of the Ras-like GTPase Rap1, involved in Cerebral Cavernous Malformations (CCM). We present evidences that miR-21 sil...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Academic Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3750217/ https://www.ncbi.nlm.nih.gov/pubmed/23872064 http://dx.doi.org/10.1016/j.bbrc.2013.07.031 |
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author | Orso, Francesca Balzac, Fiorella Marino, Marco Lembo, Antonio Retta, Saverio Francesco Taverna, Daniela |
author_facet | Orso, Francesca Balzac, Fiorella Marino, Marco Lembo, Antonio Retta, Saverio Francesco Taverna, Daniela |
author_sort | Orso, Francesca |
collection | PubMed |
description | miR-21 is overexpressed in tumors and it displays oncogenic activity. Here, we show that expression of miR-21 in primary tumors anticorrelates with KRIT1/CCM1, an interacting partner of the Ras-like GTPase Rap1, involved in Cerebral Cavernous Malformations (CCM). We present evidences that miR-21 silences KRIT1 by targeting its mRNA 3′UTR and that this interaction is involved in tumor growth control. In fact, miR-21 over-expression or KRIT1 knock-down promote anchorage independent tumor cell growth compared to controls, whereas the opposite is observed when anti-miR-21 or KRIT1 overexpression are employed. Our findings suggest that miR-21 promotes tumor cell growth, at least in part, by down-modulating the potential tumor suppressor KRIT1. |
format | Online Article Text |
id | pubmed-3750217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Academic Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-37502172013-08-23 miR-21 coordinates tumor growth and modulates KRIT1 levels Orso, Francesca Balzac, Fiorella Marino, Marco Lembo, Antonio Retta, Saverio Francesco Taverna, Daniela Biochem Biophys Res Commun Article miR-21 is overexpressed in tumors and it displays oncogenic activity. Here, we show that expression of miR-21 in primary tumors anticorrelates with KRIT1/CCM1, an interacting partner of the Ras-like GTPase Rap1, involved in Cerebral Cavernous Malformations (CCM). We present evidences that miR-21 silences KRIT1 by targeting its mRNA 3′UTR and that this interaction is involved in tumor growth control. In fact, miR-21 over-expression or KRIT1 knock-down promote anchorage independent tumor cell growth compared to controls, whereas the opposite is observed when anti-miR-21 or KRIT1 overexpression are employed. Our findings suggest that miR-21 promotes tumor cell growth, at least in part, by down-modulating the potential tumor suppressor KRIT1. Academic Press 2013-08-16 /pmc/articles/PMC3750217/ /pubmed/23872064 http://dx.doi.org/10.1016/j.bbrc.2013.07.031 Text en © 2013 Elsevier Inc. This document may be redistributed and reused, subject to certain conditions (http://www.elsevier.com/wps/find/authorsview.authors/supplementalterms1.0) . |
spellingShingle | Article Orso, Francesca Balzac, Fiorella Marino, Marco Lembo, Antonio Retta, Saverio Francesco Taverna, Daniela miR-21 coordinates tumor growth and modulates KRIT1 levels |
title | miR-21 coordinates tumor growth and modulates KRIT1 levels |
title_full | miR-21 coordinates tumor growth and modulates KRIT1 levels |
title_fullStr | miR-21 coordinates tumor growth and modulates KRIT1 levels |
title_full_unstemmed | miR-21 coordinates tumor growth and modulates KRIT1 levels |
title_short | miR-21 coordinates tumor growth and modulates KRIT1 levels |
title_sort | mir-21 coordinates tumor growth and modulates krit1 levels |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3750217/ https://www.ncbi.nlm.nih.gov/pubmed/23872064 http://dx.doi.org/10.1016/j.bbrc.2013.07.031 |
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