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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...

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Detalles Bibliográficos
Autores principales: Orso, Francesca, Balzac, Fiorella, Marino, Marco, Lembo, Antonio, Retta, Saverio Francesco, Taverna, Daniela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academic Press 2013
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.
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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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