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Claudin-10 is a new candidate prognostic marker in metastatic high-grade serous carcinoma
The objective of this study was to analyze the expression and prognostic role of the tight junction protein claudin-10 in high-grade serous carcinoma (HGSC). Claudin-10 protein expression by immunohistochemistry was analyzed in 588 HGSC (414 effusions, 174 surgical specimens). Expression in mesothel...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10247576/ https://www.ncbi.nlm.nih.gov/pubmed/37067588 http://dx.doi.org/10.1007/s00428-023-03541-6 |
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author | Davidson, Ben Doutel, Delfim Holth, Arild Nymoen, Dag Andre |
author_facet | Davidson, Ben Doutel, Delfim Holth, Arild Nymoen, Dag Andre |
author_sort | Davidson, Ben |
collection | PubMed |
description | The objective of this study was to analyze the expression and prognostic role of the tight junction protein claudin-10 in high-grade serous carcinoma (HGSC). Claudin-10 protein expression by immunohistochemistry was analyzed in 588 HGSC (414 effusions, 174 surgical specimens). Expression in mesotheliomas (n = 97; 47 effusions, 50 surgical specimens) was studied for comparative purposes. CLDN10 mRNA expression by quantitative RT-PCR (qRT-PCR) was analyzed in 40 HGSC effusions. Claudin-10 protein expression was found in 360/588 (61%) HGSC vs. 19/97 (20%) mesotheliomas (p < 0.001), and was higher in HGSC surgical specimens compared to effusions (p < 0.001). qRT-PCR confirmed the presence of CLDN10 mRNA in HGSC effusions. High (> 25%) claudin-10 expression in HGSC effusions was significantly associated with shorter overall survival (OS; p = 0.036) and progression-free survival (PFS; p = 0.045) in univariate analysis, and was an independent prognosticator of OS in multivariate analysis (p = 0.045). In conclusion, claudin-10 protein expression is higher in HGSC compared to mesothelioma, although the diagnostic power of this marker appear to be lesser than other claudin family members. Claudin-10 expression in HGSC effusions is marker of more aggressive disease. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00428-023-03541-6. |
format | Online Article Text |
id | pubmed-10247576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-102475762023-06-09 Claudin-10 is a new candidate prognostic marker in metastatic high-grade serous carcinoma Davidson, Ben Doutel, Delfim Holth, Arild Nymoen, Dag Andre Virchows Arch Original Article The objective of this study was to analyze the expression and prognostic role of the tight junction protein claudin-10 in high-grade serous carcinoma (HGSC). Claudin-10 protein expression by immunohistochemistry was analyzed in 588 HGSC (414 effusions, 174 surgical specimens). Expression in mesotheliomas (n = 97; 47 effusions, 50 surgical specimens) was studied for comparative purposes. CLDN10 mRNA expression by quantitative RT-PCR (qRT-PCR) was analyzed in 40 HGSC effusions. Claudin-10 protein expression was found in 360/588 (61%) HGSC vs. 19/97 (20%) mesotheliomas (p < 0.001), and was higher in HGSC surgical specimens compared to effusions (p < 0.001). qRT-PCR confirmed the presence of CLDN10 mRNA in HGSC effusions. High (> 25%) claudin-10 expression in HGSC effusions was significantly associated with shorter overall survival (OS; p = 0.036) and progression-free survival (PFS; p = 0.045) in univariate analysis, and was an independent prognosticator of OS in multivariate analysis (p = 0.045). In conclusion, claudin-10 protein expression is higher in HGSC compared to mesothelioma, although the diagnostic power of this marker appear to be lesser than other claudin family members. Claudin-10 expression in HGSC effusions is marker of more aggressive disease. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00428-023-03541-6. Springer Berlin Heidelberg 2023-04-17 2023 /pmc/articles/PMC10247576/ /pubmed/37067588 http://dx.doi.org/10.1007/s00428-023-03541-6 Text en © The Author(s) 2023, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Davidson, Ben Doutel, Delfim Holth, Arild Nymoen, Dag Andre Claudin-10 is a new candidate prognostic marker in metastatic high-grade serous carcinoma |
title | Claudin-10 is a new candidate prognostic marker in metastatic high-grade serous carcinoma |
title_full | Claudin-10 is a new candidate prognostic marker in metastatic high-grade serous carcinoma |
title_fullStr | Claudin-10 is a new candidate prognostic marker in metastatic high-grade serous carcinoma |
title_full_unstemmed | Claudin-10 is a new candidate prognostic marker in metastatic high-grade serous carcinoma |
title_short | Claudin-10 is a new candidate prognostic marker in metastatic high-grade serous carcinoma |
title_sort | claudin-10 is a new candidate prognostic marker in metastatic high-grade serous carcinoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10247576/ https://www.ncbi.nlm.nih.gov/pubmed/37067588 http://dx.doi.org/10.1007/s00428-023-03541-6 |
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