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Relevance of IGFBP2 proteolysis in glioma and contribution of the extracellular protease ADAMTS1
Expression of IGFBP2 (Insulin-like Growth Factor Binding Protein 2) has been positively correlated with glioma progression. Although the proteolysis of IGFBP2 has been widely recognized, with consequences as a major modulator of IGFII signaling, the relevance of this post-translational modification...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147324/ https://www.ncbi.nlm.nih.gov/pubmed/24962328 |
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author | Martino-Echarri, Estefanía Fernández-Rodríguez, Rubén Bech-Serra, Joan Josep Plaza-Calonge, María del Carmen Vidal, Noemi Casal, Carmen Colomé, Nuria Seoane, Joan Canals, Francesc Rodríguez-Manzaneque, Juan Carlos |
author_facet | Martino-Echarri, Estefanía Fernández-Rodríguez, Rubén Bech-Serra, Joan Josep Plaza-Calonge, María del Carmen Vidal, Noemi Casal, Carmen Colomé, Nuria Seoane, Joan Canals, Francesc Rodríguez-Manzaneque, Juan Carlos |
author_sort | Martino-Echarri, Estefanía |
collection | PubMed |
description | Expression of IGFBP2 (Insulin-like Growth Factor Binding Protein 2) has been positively correlated with glioma progression. Although the proteolysis of IGFBP2 has been widely recognized, with consequences as a major modulator of IGFII signaling, the relevance of this post-translational modification has not been well studied in tumors. Using an in vivo proteomic approach by Isotope-Coded Protein Label (ICPL), we identified IGFBP2 as a target of the extracellular protease ADAMTS1 (A Disintegrin And Metalloproteinase with ThromboSpondin motifs 1). Notably, the proteolytic pattern of IGFBP2 was also detected in human glioma culture cells and, more importantly, in all glioma samples evaluated. In addition, high expression of ADAMTS1 correlates with higher levels of cleaved IGFBP2 in glioblastoma multiforme cases. Using gene expression public databases, we confirmed that IGFBP2 is a poor prognosis marker for gliomas, and we also observed an important contribution of ADAMTS1.Finally, we showed the impact of ADAMTS1 on IGFII-mediated IGF1R phosphorylation and cellular migration. Our results support a functional interaction between IGFBP2 and ADAMTS1 and suggest the need to evaluate post-translational modifications of IGFBP2 in glioma, in order to approach new therapies. |
format | Online Article Text |
id | pubmed-4147324 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-41473242014-08-29 Relevance of IGFBP2 proteolysis in glioma and contribution of the extracellular protease ADAMTS1 Martino-Echarri, Estefanía Fernández-Rodríguez, Rubén Bech-Serra, Joan Josep Plaza-Calonge, María del Carmen Vidal, Noemi Casal, Carmen Colomé, Nuria Seoane, Joan Canals, Francesc Rodríguez-Manzaneque, Juan Carlos Oncotarget Research Paper Expression of IGFBP2 (Insulin-like Growth Factor Binding Protein 2) has been positively correlated with glioma progression. Although the proteolysis of IGFBP2 has been widely recognized, with consequences as a major modulator of IGFII signaling, the relevance of this post-translational modification has not been well studied in tumors. Using an in vivo proteomic approach by Isotope-Coded Protein Label (ICPL), we identified IGFBP2 as a target of the extracellular protease ADAMTS1 (A Disintegrin And Metalloproteinase with ThromboSpondin motifs 1). Notably, the proteolytic pattern of IGFBP2 was also detected in human glioma culture cells and, more importantly, in all glioma samples evaluated. In addition, high expression of ADAMTS1 correlates with higher levels of cleaved IGFBP2 in glioblastoma multiforme cases. Using gene expression public databases, we confirmed that IGFBP2 is a poor prognosis marker for gliomas, and we also observed an important contribution of ADAMTS1.Finally, we showed the impact of ADAMTS1 on IGFII-mediated IGF1R phosphorylation and cellular migration. Our results support a functional interaction between IGFBP2 and ADAMTS1 and suggest the need to evaluate post-translational modifications of IGFBP2 in glioma, in order to approach new therapies. Impact Journals LLC 2014-05-26 /pmc/articles/PMC4147324/ /pubmed/24962328 Text en Copyright: © 2014 Martino-Echarri et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Martino-Echarri, Estefanía Fernández-Rodríguez, Rubén Bech-Serra, Joan Josep Plaza-Calonge, María del Carmen Vidal, Noemi Casal, Carmen Colomé, Nuria Seoane, Joan Canals, Francesc Rodríguez-Manzaneque, Juan Carlos Relevance of IGFBP2 proteolysis in glioma and contribution of the extracellular protease ADAMTS1 |
title | Relevance of IGFBP2 proteolysis in glioma and contribution of the extracellular protease ADAMTS1 |
title_full | Relevance of IGFBP2 proteolysis in glioma and contribution of the extracellular protease ADAMTS1 |
title_fullStr | Relevance of IGFBP2 proteolysis in glioma and contribution of the extracellular protease ADAMTS1 |
title_full_unstemmed | Relevance of IGFBP2 proteolysis in glioma and contribution of the extracellular protease ADAMTS1 |
title_short | Relevance of IGFBP2 proteolysis in glioma and contribution of the extracellular protease ADAMTS1 |
title_sort | relevance of igfbp2 proteolysis in glioma and contribution of the extracellular protease adamts1 |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147324/ https://www.ncbi.nlm.nih.gov/pubmed/24962328 |
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