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CIAPIN1 and ABCA13 are markers of poor survival in metastatic ovarian serous carcinoma
BACKGROUND: The objective of this study was to investigate the expression and clinical role of 14 genes previously shown to be associated with chemotherapy response and/or progression-free survival in a smaller series of ovarian serous carcinoma effusions. METHODS: Advanced-stage serous ovarian carc...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4336750/ https://www.ncbi.nlm.nih.gov/pubmed/25889687 http://dx.doi.org/10.1186/s12943-015-0317-1 |
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author | Nymoen, Dag Andre Holth, Arild Hetland Falkenthal, Thea E Tropé, Claes G Davidson, Ben |
author_facet | Nymoen, Dag Andre Holth, Arild Hetland Falkenthal, Thea E Tropé, Claes G Davidson, Ben |
author_sort | Nymoen, Dag Andre |
collection | PubMed |
description | BACKGROUND: The objective of this study was to investigate the expression and clinical role of 14 genes previously shown to be associated with chemotherapy response and/or progression-free survival in a smaller series of ovarian serous carcinoma effusions. METHODS: Advanced-stage serous ovarian carcinoma effusions (n = 150) were analyzed for mRNA expression of AKR1C1, ABCA4, ABCA13, ABCB10, BIRC6, CASP9, CIAPIN1, FAS, MGMT, MUTYH, POLH, SRC, TBRKB and XPA using quantitative real-time PCR. mRNA expression was studied for association with clinicopathologic parameters, including chemotherapy response and survival. RESULTS: ABCA4 mRNA expression was significantly related to better (complete) chemotherapy response at diagnosis in the entire cohort (p = 0.018), whereas higher POLH mRNA levels were significantly related to better chemoresponse at diagnosis in analysis to 58 patients with pre-chemotherapy effusions treated with standard chemotherapy (carboplatin + paclitaxel; p = 0.023). In univariate survival analysis for patients with pre-chemotherapy effusions (n = 77), CIAPIN1 mRNA expression was significantly related to shorter overall (p = 0.007) and progression-free (p = 0.038) survival, whereas ABCA13 mRNA expression was significantly related to shorter OS (p = 0.024). Higher CIAPIN1 mRNA expression was an independent marker of poor overall survival in Cox multivariate analysis (p = 0.044). CONCLUSIONS: Our data identify ABCA4 and POLH as markers of better chemotherapy response in metastatic serous carcinoma. CIAPIN1 and ABCA13 may be novel markers of poor outcome in pre-chemotherapy serous carcinoma effusions. |
format | Online Article Text |
id | pubmed-4336750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43367502015-02-23 CIAPIN1 and ABCA13 are markers of poor survival in metastatic ovarian serous carcinoma Nymoen, Dag Andre Holth, Arild Hetland Falkenthal, Thea E Tropé, Claes G Davidson, Ben Mol Cancer Research BACKGROUND: The objective of this study was to investigate the expression and clinical role of 14 genes previously shown to be associated with chemotherapy response and/or progression-free survival in a smaller series of ovarian serous carcinoma effusions. METHODS: Advanced-stage serous ovarian carcinoma effusions (n = 150) were analyzed for mRNA expression of AKR1C1, ABCA4, ABCA13, ABCB10, BIRC6, CASP9, CIAPIN1, FAS, MGMT, MUTYH, POLH, SRC, TBRKB and XPA using quantitative real-time PCR. mRNA expression was studied for association with clinicopathologic parameters, including chemotherapy response and survival. RESULTS: ABCA4 mRNA expression was significantly related to better (complete) chemotherapy response at diagnosis in the entire cohort (p = 0.018), whereas higher POLH mRNA levels were significantly related to better chemoresponse at diagnosis in analysis to 58 patients with pre-chemotherapy effusions treated with standard chemotherapy (carboplatin + paclitaxel; p = 0.023). In univariate survival analysis for patients with pre-chemotherapy effusions (n = 77), CIAPIN1 mRNA expression was significantly related to shorter overall (p = 0.007) and progression-free (p = 0.038) survival, whereas ABCA13 mRNA expression was significantly related to shorter OS (p = 0.024). Higher CIAPIN1 mRNA expression was an independent marker of poor overall survival in Cox multivariate analysis (p = 0.044). CONCLUSIONS: Our data identify ABCA4 and POLH as markers of better chemotherapy response in metastatic serous carcinoma. CIAPIN1 and ABCA13 may be novel markers of poor outcome in pre-chemotherapy serous carcinoma effusions. BioMed Central 2015-02-18 /pmc/articles/PMC4336750/ /pubmed/25889687 http://dx.doi.org/10.1186/s12943-015-0317-1 Text en © Nymoen et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Nymoen, Dag Andre Holth, Arild Hetland Falkenthal, Thea E Tropé, Claes G Davidson, Ben CIAPIN1 and ABCA13 are markers of poor survival in metastatic ovarian serous carcinoma |
title | CIAPIN1 and ABCA13 are markers of poor survival in metastatic ovarian serous carcinoma |
title_full | CIAPIN1 and ABCA13 are markers of poor survival in metastatic ovarian serous carcinoma |
title_fullStr | CIAPIN1 and ABCA13 are markers of poor survival in metastatic ovarian serous carcinoma |
title_full_unstemmed | CIAPIN1 and ABCA13 are markers of poor survival in metastatic ovarian serous carcinoma |
title_short | CIAPIN1 and ABCA13 are markers of poor survival in metastatic ovarian serous carcinoma |
title_sort | ciapin1 and abca13 are markers of poor survival in metastatic ovarian serous carcinoma |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4336750/ https://www.ncbi.nlm.nih.gov/pubmed/25889687 http://dx.doi.org/10.1186/s12943-015-0317-1 |
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