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Tissue and plasma levels of galectins in patients with high grade serous ovarian carcinoma as new predictive biomarkers

Galectins are moving closer to center stage in detecting glycosylation aberration in cancer cells. Here, we have investigated the expression of galectins in ovarian cancer (OC) and examined their potential as biomarkers in tissues and blood plasma samples of high grade serous ovarian carcinoma (HGSC...

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Autores principales: Labrie, Marilyne, De Araujo, Lorenna Oliveira Fernandes, Communal, Laudine, Mes-Masson, Anne-Marie, St-Pierre, Yves
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5643335/
https://www.ncbi.nlm.nih.gov/pubmed/29038585
http://dx.doi.org/10.1038/s41598-017-13802-5
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author Labrie, Marilyne
De Araujo, Lorenna Oliveira Fernandes
Communal, Laudine
Mes-Masson, Anne-Marie
St-Pierre, Yves
author_facet Labrie, Marilyne
De Araujo, Lorenna Oliveira Fernandes
Communal, Laudine
Mes-Masson, Anne-Marie
St-Pierre, Yves
author_sort Labrie, Marilyne
collection PubMed
description Galectins are moving closer to center stage in detecting glycosylation aberration in cancer cells. Here, we have investigated the expression of galectins in ovarian cancer (OC) and examined their potential as biomarkers in tissues and blood plasma samples of high grade serous ovarian carcinoma (HGSC) patients. In tissues, we found that increased protein expression of stromal gal-1 and epithelial gal-8/9 was associated with a poor response to treatment of HGSC patients. Gal-8/9 were both independent predictors of chemoresistance and overall survival (OS), respectively. This galectin signature increased the predictive value of the cancer antigen 125 (CA125) on 5-year disease-free survival (DFS), post-chemotherapy treatment and 5-year OS. In CA125(LOW) patients, epithelial gal-9 was associated with a lower 5-year OS while stromal gal-1 and epithelial gal-8 were both associated with a lower 5-year DFS. Such negative predictive value of gal-8 and gal-9 was also found using plasma samples. In both cases, high plasma levels of gal-8 and gal-9 was associated with a lower OS and DFS. Overall, these data suggest that galectins may be promising biomarkers to identify subgroups of HGSC patients with poorer prognosis. Our study also contributes to better define the heterogeneity of the disease.
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spelling pubmed-56433352017-10-19 Tissue and plasma levels of galectins in patients with high grade serous ovarian carcinoma as new predictive biomarkers Labrie, Marilyne De Araujo, Lorenna Oliveira Fernandes Communal, Laudine Mes-Masson, Anne-Marie St-Pierre, Yves Sci Rep Article Galectins are moving closer to center stage in detecting glycosylation aberration in cancer cells. Here, we have investigated the expression of galectins in ovarian cancer (OC) and examined their potential as biomarkers in tissues and blood plasma samples of high grade serous ovarian carcinoma (HGSC) patients. In tissues, we found that increased protein expression of stromal gal-1 and epithelial gal-8/9 was associated with a poor response to treatment of HGSC patients. Gal-8/9 were both independent predictors of chemoresistance and overall survival (OS), respectively. This galectin signature increased the predictive value of the cancer antigen 125 (CA125) on 5-year disease-free survival (DFS), post-chemotherapy treatment and 5-year OS. In CA125(LOW) patients, epithelial gal-9 was associated with a lower 5-year OS while stromal gal-1 and epithelial gal-8 were both associated with a lower 5-year DFS. Such negative predictive value of gal-8 and gal-9 was also found using plasma samples. In both cases, high plasma levels of gal-8 and gal-9 was associated with a lower OS and DFS. Overall, these data suggest that galectins may be promising biomarkers to identify subgroups of HGSC patients with poorer prognosis. Our study also contributes to better define the heterogeneity of the disease. Nature Publishing Group UK 2017-10-16 /pmc/articles/PMC5643335/ /pubmed/29038585 http://dx.doi.org/10.1038/s41598-017-13802-5 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
Labrie, Marilyne
De Araujo, Lorenna Oliveira Fernandes
Communal, Laudine
Mes-Masson, Anne-Marie
St-Pierre, Yves
Tissue and plasma levels of galectins in patients with high grade serous ovarian carcinoma as new predictive biomarkers
title Tissue and plasma levels of galectins in patients with high grade serous ovarian carcinoma as new predictive biomarkers
title_full Tissue and plasma levels of galectins in patients with high grade serous ovarian carcinoma as new predictive biomarkers
title_fullStr Tissue and plasma levels of galectins in patients with high grade serous ovarian carcinoma as new predictive biomarkers
title_full_unstemmed Tissue and plasma levels of galectins in patients with high grade serous ovarian carcinoma as new predictive biomarkers
title_short Tissue and plasma levels of galectins in patients with high grade serous ovarian carcinoma as new predictive biomarkers
title_sort tissue and plasma levels of galectins in patients with high grade serous ovarian carcinoma as new predictive biomarkers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5643335/
https://www.ncbi.nlm.nih.gov/pubmed/29038585
http://dx.doi.org/10.1038/s41598-017-13802-5
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