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Osteopontin-a splice variant is overexpressed in papillary thyroid carcinoma and modulates invasive behavior

Osteopontin (OPN) is a matricellular protein overexpressed in cancer cells and modulates tumorigenesis and metastasis, including in thyroid cancer (TC). The contribution of each OPN splice variant (OPN-SV), named OPNa, OPNb and OPNc, in TC is currently unknown. This study evaluates the expression of...

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Autores principales: Ferreira, Luciana Bueno, Tavares, Catarina, Pestana, Ana, Pereira, Catarina Leite, Eloy, Catarina, Pinto, Marta Teixeira, Castro, Patricia, Batista, Rui, Rios, Elisabete, Sobrinho-Simões, Manuel, Pereira Gimba, Etel Rodrigues, Soares, Paula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5239531/
https://www.ncbi.nlm.nih.gov/pubmed/27409830
http://dx.doi.org/10.18632/oncotarget.10468
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author Ferreira, Luciana Bueno
Tavares, Catarina
Pestana, Ana
Pereira, Catarina Leite
Eloy, Catarina
Pinto, Marta Teixeira
Castro, Patricia
Batista, Rui
Rios, Elisabete
Sobrinho-Simões, Manuel
Pereira Gimba, Etel Rodrigues
Soares, Paula
author_facet Ferreira, Luciana Bueno
Tavares, Catarina
Pestana, Ana
Pereira, Catarina Leite
Eloy, Catarina
Pinto, Marta Teixeira
Castro, Patricia
Batista, Rui
Rios, Elisabete
Sobrinho-Simões, Manuel
Pereira Gimba, Etel Rodrigues
Soares, Paula
author_sort Ferreira, Luciana Bueno
collection PubMed
description Osteopontin (OPN) is a matricellular protein overexpressed in cancer cells and modulates tumorigenesis and metastasis, including in thyroid cancer (TC). The contribution of each OPN splice variant (OPN-SV), named OPNa, OPNb and OPNc, in TC is currently unknown. This study evaluates the expression of total OPN (tOPN) and OPN-SV in TC tissues and cell lines, their correlation with clinicopathological, molecular features and their functional roles. We showed that tOPN and OPNa are overexpressed in classic papillary thyroid carcinoma (cPTC) in relation to adjacent thyroid, adenoma and follicular variant of papillary thyroid carcinoma (fvPTC) tissues. In cPTC, OPNa overexpression is associated with larger tumor size, vascular invasion, extrathyroid extension and BRAF(V600E) mutation. We found that TC cell lines overexpressing OPNa exhibited increased proliferation, migration, motility and in vivo invasion. Conditioned medium secreted from cells overexpressing OPNa induce MMP2 and MMP9 metalloproteinases activity. In summary, we described the expression pattern of OPN-SV in cPTC samples and the key role of OPNa expression on activating TC tumor progression features. Our findings highlight OPNa variant as TC biomarker, besides being a putative target for cPTC therapeutic approaches.
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spelling pubmed-52395312017-01-24 Osteopontin-a splice variant is overexpressed in papillary thyroid carcinoma and modulates invasive behavior Ferreira, Luciana Bueno Tavares, Catarina Pestana, Ana Pereira, Catarina Leite Eloy, Catarina Pinto, Marta Teixeira Castro, Patricia Batista, Rui Rios, Elisabete Sobrinho-Simões, Manuel Pereira Gimba, Etel Rodrigues Soares, Paula Oncotarget Research Paper Osteopontin (OPN) is a matricellular protein overexpressed in cancer cells and modulates tumorigenesis and metastasis, including in thyroid cancer (TC). The contribution of each OPN splice variant (OPN-SV), named OPNa, OPNb and OPNc, in TC is currently unknown. This study evaluates the expression of total OPN (tOPN) and OPN-SV in TC tissues and cell lines, their correlation with clinicopathological, molecular features and their functional roles. We showed that tOPN and OPNa are overexpressed in classic papillary thyroid carcinoma (cPTC) in relation to adjacent thyroid, adenoma and follicular variant of papillary thyroid carcinoma (fvPTC) tissues. In cPTC, OPNa overexpression is associated with larger tumor size, vascular invasion, extrathyroid extension and BRAF(V600E) mutation. We found that TC cell lines overexpressing OPNa exhibited increased proliferation, migration, motility and in vivo invasion. Conditioned medium secreted from cells overexpressing OPNa induce MMP2 and MMP9 metalloproteinases activity. In summary, we described the expression pattern of OPN-SV in cPTC samples and the key role of OPNa expression on activating TC tumor progression features. Our findings highlight OPNa variant as TC biomarker, besides being a putative target for cPTC therapeutic approaches. Impact Journals LLC 2016-07-07 /pmc/articles/PMC5239531/ /pubmed/27409830 http://dx.doi.org/10.18632/oncotarget.10468 Text en Copyright: © 2016 Ferreira 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
Ferreira, Luciana Bueno
Tavares, Catarina
Pestana, Ana
Pereira, Catarina Leite
Eloy, Catarina
Pinto, Marta Teixeira
Castro, Patricia
Batista, Rui
Rios, Elisabete
Sobrinho-Simões, Manuel
Pereira Gimba, Etel Rodrigues
Soares, Paula
Osteopontin-a splice variant is overexpressed in papillary thyroid carcinoma and modulates invasive behavior
title Osteopontin-a splice variant is overexpressed in papillary thyroid carcinoma and modulates invasive behavior
title_full Osteopontin-a splice variant is overexpressed in papillary thyroid carcinoma and modulates invasive behavior
title_fullStr Osteopontin-a splice variant is overexpressed in papillary thyroid carcinoma and modulates invasive behavior
title_full_unstemmed Osteopontin-a splice variant is overexpressed in papillary thyroid carcinoma and modulates invasive behavior
title_short Osteopontin-a splice variant is overexpressed in papillary thyroid carcinoma and modulates invasive behavior
title_sort osteopontin-a splice variant is overexpressed in papillary thyroid carcinoma and modulates invasive behavior
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5239531/
https://www.ncbi.nlm.nih.gov/pubmed/27409830
http://dx.doi.org/10.18632/oncotarget.10468
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