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External validation suggests Integrin beta 3 as prognostic biomarker in serous ovarian adenocarcinomas
BACKGROUND: The majority of women with ovarian cancer are diagnosed in late stages, and the mortality rate is high. The use of biomarkers as prognostic factors may improve the treatment and clinical outcome of these patients. We performed an external validation of the potential biomarkers CLU, ITGB3...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2754489/ https://www.ncbi.nlm.nih.gov/pubmed/19775429 http://dx.doi.org/10.1186/1471-2407-9-336 |
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author | Partheen, Karolina Levan, Kristina Österberg, Lovisa Claesson, Ingela Sundfeldt, Karin Horvath, György |
author_facet | Partheen, Karolina Levan, Kristina Österberg, Lovisa Claesson, Ingela Sundfeldt, Karin Horvath, György |
author_sort | Partheen, Karolina |
collection | PubMed |
description | BACKGROUND: The majority of women with ovarian cancer are diagnosed in late stages, and the mortality rate is high. The use of biomarkers as prognostic factors may improve the treatment and clinical outcome of these patients. We performed an external validation of the potential biomarkers CLU, ITGB3, CAPG, and PRAME to determine if the expression levels are relevant to use as prognostic factors. METHODS: We analysed the gene expression of CLU, ITGB3, CAPG, and PRAME in 30 advanced staged serous adenocarcinomas with quantitative real-time polymerase chain reaction (QPCR) and the protein levels were analysed in 98 serous adenocarcinomas with western blot for semiquantitative analysis. Statistical differences in mRNA and protein expressions between tumours from survivors and tumours from deceased patients were evaluated using the Mann-Whitney U test. RESULTS: The gene and protein ITGB3 (Integrin beta 3) were significantly more expressed in tumours from survivors compared to tumours from deceased patients, which is in concordance with our previous results. However, no significant differences were detected for the other three genes or proteins CLU, CAPG, and PRAME. CONCLUSION: The loss of ITGB3 expression in tumours from deceased patients and high expression in tumours from survivors could be used as a biomarker for patients with advanced serous tumours. |
format | Text |
id | pubmed-2754489 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27544892009-09-30 External validation suggests Integrin beta 3 as prognostic biomarker in serous ovarian adenocarcinomas Partheen, Karolina Levan, Kristina Österberg, Lovisa Claesson, Ingela Sundfeldt, Karin Horvath, György BMC Cancer Research Article BACKGROUND: The majority of women with ovarian cancer are diagnosed in late stages, and the mortality rate is high. The use of biomarkers as prognostic factors may improve the treatment and clinical outcome of these patients. We performed an external validation of the potential biomarkers CLU, ITGB3, CAPG, and PRAME to determine if the expression levels are relevant to use as prognostic factors. METHODS: We analysed the gene expression of CLU, ITGB3, CAPG, and PRAME in 30 advanced staged serous adenocarcinomas with quantitative real-time polymerase chain reaction (QPCR) and the protein levels were analysed in 98 serous adenocarcinomas with western blot for semiquantitative analysis. Statistical differences in mRNA and protein expressions between tumours from survivors and tumours from deceased patients were evaluated using the Mann-Whitney U test. RESULTS: The gene and protein ITGB3 (Integrin beta 3) were significantly more expressed in tumours from survivors compared to tumours from deceased patients, which is in concordance with our previous results. However, no significant differences were detected for the other three genes or proteins CLU, CAPG, and PRAME. CONCLUSION: The loss of ITGB3 expression in tumours from deceased patients and high expression in tumours from survivors could be used as a biomarker for patients with advanced serous tumours. BioMed Central 2009-09-23 /pmc/articles/PMC2754489/ /pubmed/19775429 http://dx.doi.org/10.1186/1471-2407-9-336 Text en Copyright ©2009 Partheen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Partheen, Karolina Levan, Kristina Österberg, Lovisa Claesson, Ingela Sundfeldt, Karin Horvath, György External validation suggests Integrin beta 3 as prognostic biomarker in serous ovarian adenocarcinomas |
title | External validation suggests Integrin beta 3 as prognostic biomarker in serous ovarian adenocarcinomas |
title_full | External validation suggests Integrin beta 3 as prognostic biomarker in serous ovarian adenocarcinomas |
title_fullStr | External validation suggests Integrin beta 3 as prognostic biomarker in serous ovarian adenocarcinomas |
title_full_unstemmed | External validation suggests Integrin beta 3 as prognostic biomarker in serous ovarian adenocarcinomas |
title_short | External validation suggests Integrin beta 3 as prognostic biomarker in serous ovarian adenocarcinomas |
title_sort | external validation suggests integrin beta 3 as prognostic biomarker in serous ovarian adenocarcinomas |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2754489/ https://www.ncbi.nlm.nih.gov/pubmed/19775429 http://dx.doi.org/10.1186/1471-2407-9-336 |
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