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Mucin-1 and its relation to grade, stage and survival in ovarian carcinoma patients
BACKGROUND: Mucin-1 is known to be over-expressed by various human carcinomas and is shed into the circulation where it can be detected in patient’s serum by specific anti-Mucin-1 antibodies, such as the tumour marker assays CA 15–3 and CA 27.29. The prognostic value of Mucin-1 expression in ovarian...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3582552/ https://www.ncbi.nlm.nih.gov/pubmed/23241107 http://dx.doi.org/10.1186/1471-2407-12-600 |
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author | Engelstaedter, Verena Heublein, Sabine Schumacher, Anamur Lan Lenhard, Miriam Engelstaedter, Helen Andergassen, Ulrich Guenthner-Biller, Margit Kuhn, Christina Rack, Brigitte Kupka, Markus Mayr, Doris Jeschke, Udo |
author_facet | Engelstaedter, Verena Heublein, Sabine Schumacher, Anamur Lan Lenhard, Miriam Engelstaedter, Helen Andergassen, Ulrich Guenthner-Biller, Margit Kuhn, Christina Rack, Brigitte Kupka, Markus Mayr, Doris Jeschke, Udo |
author_sort | Engelstaedter, Verena |
collection | PubMed |
description | BACKGROUND: Mucin-1 is known to be over-expressed by various human carcinomas and is shed into the circulation where it can be detected in patient’s serum by specific anti-Mucin-1 antibodies, such as the tumour marker assays CA 15–3 and CA 27.29. The prognostic value of Mucin-1 expression in ovarian carcinoma remains uncertain. One aim of this study was to compare the concentrations of Mucin-1 in a cohort of patients with either benign or malignant ovarian tumours detected by CA 15–3 and CA 27.29. Another aim of this study was to evaluate Mucin-1 expression by immunohistochemistry in a different cohort of ovarian carcinoma patients with respect to grade, stage and survival. METHODS: Patients diagnosed with and treated for ovarian tumours were included in the study. Patient characteristics, histology including histological subtype, tumour stage, grading and follow-up data were available from patient records. Serum Mucin-1 concentrations were measured with ELISA technology detecting CA 15–3 and CA 27.29, Mucin-1 tissue expression was determined by immunohistochemistry using the VU4H5 and VU3C6 anti-Mucin-1 antibodies. Statistical analysis was performed by using SPSS 18.0. RESULTS: Serum samples of 118 patients with ovarian tumours were obtained to determine levels of Mucin-1. Median CA 15–3 and CA 27.29 concentrations were significantly higher in patients with malignant disease (p< 0.001) than in patients with benign disease. Paraffin-embedded tissue of 154 patients with ovarian carcinoma was available to determine Mucin-1 expression. The majority of patients presented with advanced stage disease at primary diagnosis. Median follow-up time was 11.39 years. Immunohistochemistry results for VU4H5 showed significant differences with respect to tumour grade, FIGO stage and overall survival. Patients with negative expression had a mean overall survival of 9.33 years compared to 6.27 years for patients with positive Mucin-1 expression. CONCLUSIONS: This study found significantly elevated Mucin-1 serum concentrations in ovarian carcinoma patients as compared to those women suffering from benign ovarian diseases. However, it needs to be noted that Mucin-1 concentrations in carcinoma patients showed a rather high variability. Results from immunohistochemistry indicate that Mucin-1 has a prognostic relevance in ovarian carcinomas when evaluating the expression by VU4H5 antibody. |
format | Online Article Text |
id | pubmed-3582552 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35825522013-02-27 Mucin-1 and its relation to grade, stage and survival in ovarian carcinoma patients Engelstaedter, Verena Heublein, Sabine Schumacher, Anamur Lan Lenhard, Miriam Engelstaedter, Helen Andergassen, Ulrich Guenthner-Biller, Margit Kuhn, Christina Rack, Brigitte Kupka, Markus Mayr, Doris Jeschke, Udo BMC Cancer Research Article BACKGROUND: Mucin-1 is known to be over-expressed by various human carcinomas and is shed into the circulation where it can be detected in patient’s serum by specific anti-Mucin-1 antibodies, such as the tumour marker assays CA 15–3 and CA 27.29. The prognostic value of Mucin-1 expression in ovarian carcinoma remains uncertain. One aim of this study was to compare the concentrations of Mucin-1 in a cohort of patients with either benign or malignant ovarian tumours detected by CA 15–3 and CA 27.29. Another aim of this study was to evaluate Mucin-1 expression by immunohistochemistry in a different cohort of ovarian carcinoma patients with respect to grade, stage and survival. METHODS: Patients diagnosed with and treated for ovarian tumours were included in the study. Patient characteristics, histology including histological subtype, tumour stage, grading and follow-up data were available from patient records. Serum Mucin-1 concentrations were measured with ELISA technology detecting CA 15–3 and CA 27.29, Mucin-1 tissue expression was determined by immunohistochemistry using the VU4H5 and VU3C6 anti-Mucin-1 antibodies. Statistical analysis was performed by using SPSS 18.0. RESULTS: Serum samples of 118 patients with ovarian tumours were obtained to determine levels of Mucin-1. Median CA 15–3 and CA 27.29 concentrations were significantly higher in patients with malignant disease (p< 0.001) than in patients with benign disease. Paraffin-embedded tissue of 154 patients with ovarian carcinoma was available to determine Mucin-1 expression. The majority of patients presented with advanced stage disease at primary diagnosis. Median follow-up time was 11.39 years. Immunohistochemistry results for VU4H5 showed significant differences with respect to tumour grade, FIGO stage and overall survival. Patients with negative expression had a mean overall survival of 9.33 years compared to 6.27 years for patients with positive Mucin-1 expression. CONCLUSIONS: This study found significantly elevated Mucin-1 serum concentrations in ovarian carcinoma patients as compared to those women suffering from benign ovarian diseases. However, it needs to be noted that Mucin-1 concentrations in carcinoma patients showed a rather high variability. Results from immunohistochemistry indicate that Mucin-1 has a prognostic relevance in ovarian carcinomas when evaluating the expression by VU4H5 antibody. BioMed Central 2012-12-15 /pmc/articles/PMC3582552/ /pubmed/23241107 http://dx.doi.org/10.1186/1471-2407-12-600 Text en Copyright ©2012 Engelstaedter 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 Engelstaedter, Verena Heublein, Sabine Schumacher, Anamur Lan Lenhard, Miriam Engelstaedter, Helen Andergassen, Ulrich Guenthner-Biller, Margit Kuhn, Christina Rack, Brigitte Kupka, Markus Mayr, Doris Jeschke, Udo Mucin-1 and its relation to grade, stage and survival in ovarian carcinoma patients |
title | Mucin-1 and its relation to grade, stage and survival in ovarian carcinoma patients |
title_full | Mucin-1 and its relation to grade, stage and survival in ovarian carcinoma patients |
title_fullStr | Mucin-1 and its relation to grade, stage and survival in ovarian carcinoma patients |
title_full_unstemmed | Mucin-1 and its relation to grade, stage and survival in ovarian carcinoma patients |
title_short | Mucin-1 and its relation to grade, stage and survival in ovarian carcinoma patients |
title_sort | mucin-1 and its relation to grade, stage and survival in ovarian carcinoma patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3582552/ https://www.ncbi.nlm.nih.gov/pubmed/23241107 http://dx.doi.org/10.1186/1471-2407-12-600 |
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