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HMGA1 regulates the Plasminogen activation system in the secretome of breast cancer cells

Cancer cells secrete proteins that modify the extracellular environment acting as autocrine and paracrine stimulatory factors and have a relevant role in cancer progression. The HMGA1 oncofetal protein has a prominent role in controlling the expression of an articulated set of genes involved in vari...

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Autores principales: Resmini, Giulia, Rizzo, Serena, Franchin, Cinzia, Zanin, Rossella, Penzo, Carlotta, Pegoraro, Silvia, Ciani, Yari, Piazza, Silvano, Arrigoni, Giorgio, Sgarra, Riccardo, Manfioletti, Guidalberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5603555/
https://www.ncbi.nlm.nih.gov/pubmed/28924209
http://dx.doi.org/10.1038/s41598-017-11409-4
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author Resmini, Giulia
Rizzo, Serena
Franchin, Cinzia
Zanin, Rossella
Penzo, Carlotta
Pegoraro, Silvia
Ciani, Yari
Piazza, Silvano
Arrigoni, Giorgio
Sgarra, Riccardo
Manfioletti, Guidalberto
author_facet Resmini, Giulia
Rizzo, Serena
Franchin, Cinzia
Zanin, Rossella
Penzo, Carlotta
Pegoraro, Silvia
Ciani, Yari
Piazza, Silvano
Arrigoni, Giorgio
Sgarra, Riccardo
Manfioletti, Guidalberto
author_sort Resmini, Giulia
collection PubMed
description Cancer cells secrete proteins that modify the extracellular environment acting as autocrine and paracrine stimulatory factors and have a relevant role in cancer progression. The HMGA1 oncofetal protein has a prominent role in controlling the expression of an articulated set of genes involved in various aspect of cancer cell transformation. However, little is known about its role in influencing the secretome of cancer cells. Performing an iTRAQ LC–MS/MS screening for the identification of secreted proteins, in an inducible model of HMGA1 silencing in breast cancer cells, we found that HMGA1 has a profound impact on cancer cell secretome. We demonstrated that the pool of HMGA1–linked secreted proteins has pro–migratory and pro-invasive stimulatory roles. From an inspection of the HMGA1–dependent secreted factors it turned out that HMGA1 influences the presence in the extra cellular milieu of key components of the Plasminogen activation system (PLAU, SERPINE1, and PLAUR) that has a prominent role in promoting metastasis, and that HMGA1 has a direct role in regulating the transcription of two of them, i.e. PLAU and SERPINE1. The ability of HMGA1 to regulate the plasminogen activator system may constitute an important mechanism by which HMGA1 promotes cancer progression.
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spelling pubmed-56035552017-09-20 HMGA1 regulates the Plasminogen activation system in the secretome of breast cancer cells Resmini, Giulia Rizzo, Serena Franchin, Cinzia Zanin, Rossella Penzo, Carlotta Pegoraro, Silvia Ciani, Yari Piazza, Silvano Arrigoni, Giorgio Sgarra, Riccardo Manfioletti, Guidalberto Sci Rep Article Cancer cells secrete proteins that modify the extracellular environment acting as autocrine and paracrine stimulatory factors and have a relevant role in cancer progression. The HMGA1 oncofetal protein has a prominent role in controlling the expression of an articulated set of genes involved in various aspect of cancer cell transformation. However, little is known about its role in influencing the secretome of cancer cells. Performing an iTRAQ LC–MS/MS screening for the identification of secreted proteins, in an inducible model of HMGA1 silencing in breast cancer cells, we found that HMGA1 has a profound impact on cancer cell secretome. We demonstrated that the pool of HMGA1–linked secreted proteins has pro–migratory and pro-invasive stimulatory roles. From an inspection of the HMGA1–dependent secreted factors it turned out that HMGA1 influences the presence in the extra cellular milieu of key components of the Plasminogen activation system (PLAU, SERPINE1, and PLAUR) that has a prominent role in promoting metastasis, and that HMGA1 has a direct role in regulating the transcription of two of them, i.e. PLAU and SERPINE1. The ability of HMGA1 to regulate the plasminogen activator system may constitute an important mechanism by which HMGA1 promotes cancer progression. Nature Publishing Group UK 2017-09-18 /pmc/articles/PMC5603555/ /pubmed/28924209 http://dx.doi.org/10.1038/s41598-017-11409-4 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Resmini, Giulia
Rizzo, Serena
Franchin, Cinzia
Zanin, Rossella
Penzo, Carlotta
Pegoraro, Silvia
Ciani, Yari
Piazza, Silvano
Arrigoni, Giorgio
Sgarra, Riccardo
Manfioletti, Guidalberto
HMGA1 regulates the Plasminogen activation system in the secretome of breast cancer cells
title HMGA1 regulates the Plasminogen activation system in the secretome of breast cancer cells
title_full HMGA1 regulates the Plasminogen activation system in the secretome of breast cancer cells
title_fullStr HMGA1 regulates the Plasminogen activation system in the secretome of breast cancer cells
title_full_unstemmed HMGA1 regulates the Plasminogen activation system in the secretome of breast cancer cells
title_short HMGA1 regulates the Plasminogen activation system in the secretome of breast cancer cells
title_sort hmga1 regulates the plasminogen activation system in the secretome of breast cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5603555/
https://www.ncbi.nlm.nih.gov/pubmed/28924209
http://dx.doi.org/10.1038/s41598-017-11409-4
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