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High serum levels of soluble CD44 variant isoform v5 are associated with favourable clinical outcome in ovarian cancer.
In 96 ovarian cancer patients, the present study investigates the clinical significance of pretreatment concentrations of soluble CD44 standard (CD44s) and its isoforms v5 and v6 determined in the serum and the ascitic fluid by means of recently developed enzyme-linked immunosorbent assays (ELISAs)....
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1997
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2228203/ https://www.ncbi.nlm.nih.gov/pubmed/9413956 |
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author | Zeimet, A. G. Widschwendter, M. Uhl-Steidl, M. Müller-Holzner, E. Daxenbichler, G. Marth, C. Dapunt, O. |
author_facet | Zeimet, A. G. Widschwendter, M. Uhl-Steidl, M. Müller-Holzner, E. Daxenbichler, G. Marth, C. Dapunt, O. |
author_sort | Zeimet, A. G. |
collection | PubMed |
description | In 96 ovarian cancer patients, the present study investigates the clinical significance of pretreatment concentrations of soluble CD44 standard (CD44s) and its isoforms v5 and v6 determined in the serum and the ascitic fluid by means of recently developed enzyme-linked immunosorbent assays (ELISAs). Furthermore, CD44 serum concentrations in the ovarian cancer patients were compared with circulating CD44 levels in 50 healthy age-matched female blood donors. Whereas CD44s was found to be higher and CD44v5 to be lower in ovarian cancer patients than healthy control subjects, no statistical difference between the two cohorts was revealed for CD44 isoform v6. In the ascitic fluid samples, variant isoform v5 and v6 were demonstrated at lower concentrations than serum. Multivariate analysis of overall survival demonstrated that a high pretreatment serum level of soluble CD44 isoform v5 is independently associated with favourable clinical outcome in ovarian cancer. When circulating CD44 isoforms were compared with a panel of serum parameters known to be involved in the immunological network, an inverse correlation between serum CD44v5 levels and indicators of cellular immune system activation, such as soluble interleukin 2 receptor, immunostimulatory protein 90K and neopterin, became apparent. |
format | Text |
id | pubmed-2228203 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1997 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-22282032009-09-10 High serum levels of soluble CD44 variant isoform v5 are associated with favourable clinical outcome in ovarian cancer. Zeimet, A. G. Widschwendter, M. Uhl-Steidl, M. Müller-Holzner, E. Daxenbichler, G. Marth, C. Dapunt, O. Br J Cancer Research Article In 96 ovarian cancer patients, the present study investigates the clinical significance of pretreatment concentrations of soluble CD44 standard (CD44s) and its isoforms v5 and v6 determined in the serum and the ascitic fluid by means of recently developed enzyme-linked immunosorbent assays (ELISAs). Furthermore, CD44 serum concentrations in the ovarian cancer patients were compared with circulating CD44 levels in 50 healthy age-matched female blood donors. Whereas CD44s was found to be higher and CD44v5 to be lower in ovarian cancer patients than healthy control subjects, no statistical difference between the two cohorts was revealed for CD44 isoform v6. In the ascitic fluid samples, variant isoform v5 and v6 were demonstrated at lower concentrations than serum. Multivariate analysis of overall survival demonstrated that a high pretreatment serum level of soluble CD44 isoform v5 is independently associated with favourable clinical outcome in ovarian cancer. When circulating CD44 isoforms were compared with a panel of serum parameters known to be involved in the immunological network, an inverse correlation between serum CD44v5 levels and indicators of cellular immune system activation, such as soluble interleukin 2 receptor, immunostimulatory protein 90K and neopterin, became apparent. Nature Publishing Group 1997 /pmc/articles/PMC2228203/ /pubmed/9413956 Text en https://creativecommons.org/licenses/by/4.0/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 https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Zeimet, A. G. Widschwendter, M. Uhl-Steidl, M. Müller-Holzner, E. Daxenbichler, G. Marth, C. Dapunt, O. High serum levels of soluble CD44 variant isoform v5 are associated with favourable clinical outcome in ovarian cancer. |
title | High serum levels of soluble CD44 variant isoform v5 are associated with favourable clinical outcome in ovarian cancer. |
title_full | High serum levels of soluble CD44 variant isoform v5 are associated with favourable clinical outcome in ovarian cancer. |
title_fullStr | High serum levels of soluble CD44 variant isoform v5 are associated with favourable clinical outcome in ovarian cancer. |
title_full_unstemmed | High serum levels of soluble CD44 variant isoform v5 are associated with favourable clinical outcome in ovarian cancer. |
title_short | High serum levels of soluble CD44 variant isoform v5 are associated with favourable clinical outcome in ovarian cancer. |
title_sort | high serum levels of soluble cd44 variant isoform v5 are associated with favourable clinical outcome in ovarian cancer. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2228203/ https://www.ncbi.nlm.nih.gov/pubmed/9413956 |
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