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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...

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Autores principales: Davidson, Ben, Doutel, Delfim, Holth, Arild, Nymoen, Dag Andre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
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.
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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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