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MUC1 Expression by Immunohistochemistry Is Associated with Adverse Pathologic Features in Prostate Cancer: A Multi-Institutional Study
BACKGROUND: The uncertainties inherent in clinical measures of prostate cancer (CaP) aggressiveness endorse the investigation of clinically validated tissue biomarkers. MUC1 expression has been previously reported to independently predict aggressive localized prostate cancer. We used a large cohort...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5112958/ https://www.ncbi.nlm.nih.gov/pubmed/27846218 http://dx.doi.org/10.1371/journal.pone.0165236 |
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author | Eminaga, Okyaz Wei, Wei Hawley, Sarah J. Auman, Heidi Newcomb, Lisa F. Simko, Jeff Hurtado-Coll, Antonio Troyer, Dean A. Carroll, Peter R. Gleave, Martin E. Lin, Daniel W. Nelson, Peter S. Thompson, Ian M. True, Lawrence D. McKenney, Jesse K. Feng, Ziding Fazli, Ladan Brooks, James D. |
author_facet | Eminaga, Okyaz Wei, Wei Hawley, Sarah J. Auman, Heidi Newcomb, Lisa F. Simko, Jeff Hurtado-Coll, Antonio Troyer, Dean A. Carroll, Peter R. Gleave, Martin E. Lin, Daniel W. Nelson, Peter S. Thompson, Ian M. True, Lawrence D. McKenney, Jesse K. Feng, Ziding Fazli, Ladan Brooks, James D. |
author_sort | Eminaga, Okyaz |
collection | PubMed |
description | BACKGROUND: The uncertainties inherent in clinical measures of prostate cancer (CaP) aggressiveness endorse the investigation of clinically validated tissue biomarkers. MUC1 expression has been previously reported to independently predict aggressive localized prostate cancer. We used a large cohort to validate whether MUC1 protein levels measured by immunohistochemistry (IHC) predict aggressive cancer, recurrence and survival outcomes after radical prostatectomy independent of clinical and pathological parameters. MATERIAL AND METHODS: MUC1 IHC was performed on a multi-institutional tissue microarray (TMA) resource including 1,326 men with a median follow-up of 5 years. Associations with clinical and pathological parameters were tested by the Chi-square test and the Wilcoxon rank sum test. Relationships with outcome were assessed with univariable and multivariable Cox proportional hazard models and the Log-rank test. RESULTS: The presence of MUC1 expression was significantly associated with extracapsular extension and higher Gleason score, but not with seminal vesicle invasion, age, positive surgical margins or pre-operative serum PSA levels. In univariable analyses, positive MUC1 staining was significantly associated with a worse recurrence free survival (RFS) (HR: 1.24, CI 1.03–1.49, P = 0.02), although not with disease specific survival (DSS, P>0.5). On multivariable analyses, the presence of positive surgical margins, extracapsular extension, seminal vesicle invasion, as well as higher pre-operative PSA and increasing Gleason score were independently associated with RFS, while MUC1 expression was not. Positive MUC1 expression was not independently associated with disease specific survival (DSS), but was weakly associated with overall survival (OS). CONCLUSION: In our large, rigorously designed validation cohort, MUC1 protein expression was associated with adverse pathological features, although it was not an independent predictor of outcome after radical prostatectomy. |
format | Online Article Text |
id | pubmed-5112958 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-51129582016-12-08 MUC1 Expression by Immunohistochemistry Is Associated with Adverse Pathologic Features in Prostate Cancer: A Multi-Institutional Study Eminaga, Okyaz Wei, Wei Hawley, Sarah J. Auman, Heidi Newcomb, Lisa F. Simko, Jeff Hurtado-Coll, Antonio Troyer, Dean A. Carroll, Peter R. Gleave, Martin E. Lin, Daniel W. Nelson, Peter S. Thompson, Ian M. True, Lawrence D. McKenney, Jesse K. Feng, Ziding Fazli, Ladan Brooks, James D. PLoS One Research Article BACKGROUND: The uncertainties inherent in clinical measures of prostate cancer (CaP) aggressiveness endorse the investigation of clinically validated tissue biomarkers. MUC1 expression has been previously reported to independently predict aggressive localized prostate cancer. We used a large cohort to validate whether MUC1 protein levels measured by immunohistochemistry (IHC) predict aggressive cancer, recurrence and survival outcomes after radical prostatectomy independent of clinical and pathological parameters. MATERIAL AND METHODS: MUC1 IHC was performed on a multi-institutional tissue microarray (TMA) resource including 1,326 men with a median follow-up of 5 years. Associations with clinical and pathological parameters were tested by the Chi-square test and the Wilcoxon rank sum test. Relationships with outcome were assessed with univariable and multivariable Cox proportional hazard models and the Log-rank test. RESULTS: The presence of MUC1 expression was significantly associated with extracapsular extension and higher Gleason score, but not with seminal vesicle invasion, age, positive surgical margins or pre-operative serum PSA levels. In univariable analyses, positive MUC1 staining was significantly associated with a worse recurrence free survival (RFS) (HR: 1.24, CI 1.03–1.49, P = 0.02), although not with disease specific survival (DSS, P>0.5). On multivariable analyses, the presence of positive surgical margins, extracapsular extension, seminal vesicle invasion, as well as higher pre-operative PSA and increasing Gleason score were independently associated with RFS, while MUC1 expression was not. Positive MUC1 expression was not independently associated with disease specific survival (DSS), but was weakly associated with overall survival (OS). CONCLUSION: In our large, rigorously designed validation cohort, MUC1 protein expression was associated with adverse pathological features, although it was not an independent predictor of outcome after radical prostatectomy. Public Library of Science 2016-11-15 /pmc/articles/PMC5112958/ /pubmed/27846218 http://dx.doi.org/10.1371/journal.pone.0165236 Text en © 2016 Eminaga et al http://creativecommons.org/licenses/by/4.0/ 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 author and source are credited. |
spellingShingle | Research Article Eminaga, Okyaz Wei, Wei Hawley, Sarah J. Auman, Heidi Newcomb, Lisa F. Simko, Jeff Hurtado-Coll, Antonio Troyer, Dean A. Carroll, Peter R. Gleave, Martin E. Lin, Daniel W. Nelson, Peter S. Thompson, Ian M. True, Lawrence D. McKenney, Jesse K. Feng, Ziding Fazli, Ladan Brooks, James D. MUC1 Expression by Immunohistochemistry Is Associated with Adverse Pathologic Features in Prostate Cancer: A Multi-Institutional Study |
title | MUC1 Expression by Immunohistochemistry Is Associated with Adverse Pathologic Features in Prostate Cancer: A Multi-Institutional Study |
title_full | MUC1 Expression by Immunohistochemistry Is Associated with Adverse Pathologic Features in Prostate Cancer: A Multi-Institutional Study |
title_fullStr | MUC1 Expression by Immunohistochemistry Is Associated with Adverse Pathologic Features in Prostate Cancer: A Multi-Institutional Study |
title_full_unstemmed | MUC1 Expression by Immunohistochemistry Is Associated with Adverse Pathologic Features in Prostate Cancer: A Multi-Institutional Study |
title_short | MUC1 Expression by Immunohistochemistry Is Associated with Adverse Pathologic Features in Prostate Cancer: A Multi-Institutional Study |
title_sort | muc1 expression by immunohistochemistry is associated with adverse pathologic features in prostate cancer: a multi-institutional study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5112958/ https://www.ncbi.nlm.nih.gov/pubmed/27846218 http://dx.doi.org/10.1371/journal.pone.0165236 |
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