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Gene expression profile association with poor prognosis in epithelial ovarian cancer patients
Ovarian cancer (OC) is the eighth most common type of cancer for women worldwide. The current diagnostic and prognostic routine available for OC management either lack specificity or are very costly. Gene expression profiling has shown to be a very effective tool in exploring new molecular markers f...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940404/ https://www.ncbi.nlm.nih.gov/pubmed/33686173 http://dx.doi.org/10.1038/s41598-021-84953-9 |
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author | Oliveira, Douglas V. N. P. Prahm, Kira P. Christensen, Ib J. Hansen, Anker Høgdall, Claus K. Høgdall, Estrid V. |
author_facet | Oliveira, Douglas V. N. P. Prahm, Kira P. Christensen, Ib J. Hansen, Anker Høgdall, Claus K. Høgdall, Estrid V. |
author_sort | Oliveira, Douglas V. N. P. |
collection | PubMed |
description | Ovarian cancer (OC) is the eighth most common type of cancer for women worldwide. The current diagnostic and prognostic routine available for OC management either lack specificity or are very costly. Gene expression profiling has shown to be a very effective tool in exploring new molecular markers for patients with OC, although association of such markers with patient survival and clinical outcome is still elusive. Here, we performed gene expression profiling of different subtypes of OC to evaluate its association with patient overall survival (OS) and aggressive forms of the disease. By global mRNA microarray profiling in a total of 196 epithelial OC patients (161 serous, 15 endometrioid, 11 mucinous, and 9 clear cell carcinomas), we found four candidates—HSPA1A, CD99, RAB3A and POM121L9P, which associated with OS and poor clinicopathological features. The overexpression of all combined was correlated with shorter OS and progression-free survival (PFS). Furthermore, the combination of at least two markers were further associated with advanced grade, chemotherapy resistance, and progressive disease. These results indicate that a panel comprised of a few predictors that associates with a more aggressive form of OC may be clinically relevant, presenting a better performance than one marker alone. |
format | Online Article Text |
id | pubmed-7940404 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79404042021-03-10 Gene expression profile association with poor prognosis in epithelial ovarian cancer patients Oliveira, Douglas V. N. P. Prahm, Kira P. Christensen, Ib J. Hansen, Anker Høgdall, Claus K. Høgdall, Estrid V. Sci Rep Article Ovarian cancer (OC) is the eighth most common type of cancer for women worldwide. The current diagnostic and prognostic routine available for OC management either lack specificity or are very costly. Gene expression profiling has shown to be a very effective tool in exploring new molecular markers for patients with OC, although association of such markers with patient survival and clinical outcome is still elusive. Here, we performed gene expression profiling of different subtypes of OC to evaluate its association with patient overall survival (OS) and aggressive forms of the disease. By global mRNA microarray profiling in a total of 196 epithelial OC patients (161 serous, 15 endometrioid, 11 mucinous, and 9 clear cell carcinomas), we found four candidates—HSPA1A, CD99, RAB3A and POM121L9P, which associated with OS and poor clinicopathological features. The overexpression of all combined was correlated with shorter OS and progression-free survival (PFS). Furthermore, the combination of at least two markers were further associated with advanced grade, chemotherapy resistance, and progressive disease. These results indicate that a panel comprised of a few predictors that associates with a more aggressive form of OC may be clinically relevant, presenting a better performance than one marker alone. Nature Publishing Group UK 2021-03-08 /pmc/articles/PMC7940404/ /pubmed/33686173 http://dx.doi.org/10.1038/s41598-021-84953-9 Text en © The Author(s) 2021 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 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/. |
spellingShingle | Article Oliveira, Douglas V. N. P. Prahm, Kira P. Christensen, Ib J. Hansen, Anker Høgdall, Claus K. Høgdall, Estrid V. Gene expression profile association with poor prognosis in epithelial ovarian cancer patients |
title | Gene expression profile association with poor prognosis in epithelial ovarian cancer patients |
title_full | Gene expression profile association with poor prognosis in epithelial ovarian cancer patients |
title_fullStr | Gene expression profile association with poor prognosis in epithelial ovarian cancer patients |
title_full_unstemmed | Gene expression profile association with poor prognosis in epithelial ovarian cancer patients |
title_short | Gene expression profile association with poor prognosis in epithelial ovarian cancer patients |
title_sort | gene expression profile association with poor prognosis in epithelial ovarian cancer patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940404/ https://www.ncbi.nlm.nih.gov/pubmed/33686173 http://dx.doi.org/10.1038/s41598-021-84953-9 |
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