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The anti-tumor NC1 domain of collagen XIX inhibits the FAK/ PI3K/Akt/mTOR signaling pathway through αvβ3 integrin interaction
Type XIX collagen is a minor collagen associated with basement membranes. It was isolated for the first time in a human cDNA library from rhabdomyosarcoma and belongs to the FACITs family (Fibril Associated Collagens with Interrupted Triple Helices). Previously, we demonstrated that the NC1 domain o...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811477/ https://www.ncbi.nlm.nih.gov/pubmed/26621838 |
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author | Oudart, Jean-Baptiste Doué, Manon Vautrin, Alexia Brassart, Bertrand Sellier, Christèle Dupont-Deshorgue, Aurelie Monboisse, Jean-Claude Maquart, François-Xavier Brassart-Pasco, Sylvie Ramont, Laurent |
author_facet | Oudart, Jean-Baptiste Doué, Manon Vautrin, Alexia Brassart, Bertrand Sellier, Christèle Dupont-Deshorgue, Aurelie Monboisse, Jean-Claude Maquart, François-Xavier Brassart-Pasco, Sylvie Ramont, Laurent |
author_sort | Oudart, Jean-Baptiste |
collection | PubMed |
description | Type XIX collagen is a minor collagen associated with basement membranes. It was isolated for the first time in a human cDNA library from rhabdomyosarcoma and belongs to the FACITs family (Fibril Associated Collagens with Interrupted Triple Helices). Previously, we demonstrated that the NC1 domain of collagen XIX (NC1(XIX)) exerts anti-tumor properties on melanoma cells by inhibiting their migration and invasion. In the present work, we identified for the first time the integrin αvβ3 as a receptor of NC1(XIX). Moreover, we demonstrated that NC1(XIX) inhibits the FAK/PI3K/Akt/mTOR pathway, by decreasing the phosphorylation and activity of the major proteins involved in this pathway. On the other hand, NC1(XIX) induced an increase of GSK3β activity by decreasing its degree of phosphorylation. Treatments targeting this central signaling pathway in the development of melanoma are promising and new molecules should be developed. NC1(XIX) seems to have the potential for the design of new anti-cancer drugs. |
format | Online Article Text |
id | pubmed-4811477 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-48114772016-04-25 The anti-tumor NC1 domain of collagen XIX inhibits the FAK/ PI3K/Akt/mTOR signaling pathway through αvβ3 integrin interaction Oudart, Jean-Baptiste Doué, Manon Vautrin, Alexia Brassart, Bertrand Sellier, Christèle Dupont-Deshorgue, Aurelie Monboisse, Jean-Claude Maquart, François-Xavier Brassart-Pasco, Sylvie Ramont, Laurent Oncotarget Research Paper Type XIX collagen is a minor collagen associated with basement membranes. It was isolated for the first time in a human cDNA library from rhabdomyosarcoma and belongs to the FACITs family (Fibril Associated Collagens with Interrupted Triple Helices). Previously, we demonstrated that the NC1 domain of collagen XIX (NC1(XIX)) exerts anti-tumor properties on melanoma cells by inhibiting their migration and invasion. In the present work, we identified for the first time the integrin αvβ3 as a receptor of NC1(XIX). Moreover, we demonstrated that NC1(XIX) inhibits the FAK/PI3K/Akt/mTOR pathway, by decreasing the phosphorylation and activity of the major proteins involved in this pathway. On the other hand, NC1(XIX) induced an increase of GSK3β activity by decreasing its degree of phosphorylation. Treatments targeting this central signaling pathway in the development of melanoma are promising and new molecules should be developed. NC1(XIX) seems to have the potential for the design of new anti-cancer drugs. Impact Journals LLC 2015-11-26 /pmc/articles/PMC4811477/ /pubmed/26621838 Text en Copyright: © 2016 Oudart 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 Oudart, Jean-Baptiste Doué, Manon Vautrin, Alexia Brassart, Bertrand Sellier, Christèle Dupont-Deshorgue, Aurelie Monboisse, Jean-Claude Maquart, François-Xavier Brassart-Pasco, Sylvie Ramont, Laurent The anti-tumor NC1 domain of collagen XIX inhibits the FAK/ PI3K/Akt/mTOR signaling pathway through αvβ3 integrin interaction |
title | The anti-tumor NC1 domain of collagen XIX inhibits the FAK/ PI3K/Akt/mTOR signaling pathway through αvβ3 integrin interaction |
title_full | The anti-tumor NC1 domain of collagen XIX inhibits the FAK/ PI3K/Akt/mTOR signaling pathway through αvβ3 integrin interaction |
title_fullStr | The anti-tumor NC1 domain of collagen XIX inhibits the FAK/ PI3K/Akt/mTOR signaling pathway through αvβ3 integrin interaction |
title_full_unstemmed | The anti-tumor NC1 domain of collagen XIX inhibits the FAK/ PI3K/Akt/mTOR signaling pathway through αvβ3 integrin interaction |
title_short | The anti-tumor NC1 domain of collagen XIX inhibits the FAK/ PI3K/Akt/mTOR signaling pathway through αvβ3 integrin interaction |
title_sort | anti-tumor nc1 domain of collagen xix inhibits the fak/ pi3k/akt/mtor signaling pathway through αvβ3 integrin interaction |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811477/ https://www.ncbi.nlm.nih.gov/pubmed/26621838 |
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