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Tumor-Associated Macrophages Provide Significant Prognostic Information in Urothelial Bladder Cancer
Inflammation is an important feature of carcinogenesis. Tumor-associated macrophages (TAMs) can be associated with either poor or improved prognosis, depending on their properties and polarization. Current knowledge of the prognostic significance of TAMs in bladder cancer is limited and was investig...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4511010/ https://www.ncbi.nlm.nih.gov/pubmed/26197470 http://dx.doi.org/10.1371/journal.pone.0133552 |
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author | Boström, Minna M. Irjala, Heikki Mirtti, Tuomas Taimen, Pekka Kauko, Tommi Ålgars, Annika Jalkanen, Sirpa Boström, Peter J. |
author_facet | Boström, Minna M. Irjala, Heikki Mirtti, Tuomas Taimen, Pekka Kauko, Tommi Ålgars, Annika Jalkanen, Sirpa Boström, Peter J. |
author_sort | Boström, Minna M. |
collection | PubMed |
description | Inflammation is an important feature of carcinogenesis. Tumor-associated macrophages (TAMs) can be associated with either poor or improved prognosis, depending on their properties and polarization. Current knowledge of the prognostic significance of TAMs in bladder cancer is limited and was investigated in this study. We analyzed 184 urothelial bladder cancer patients undergoing transurethral resection of a bladder tumor or radical cystectomy. CD68 (pan-macrophage marker), MAC387 (polarized towards type 1 macrophages), and CLEVER-1/Stabilin-1 (type 2 macrophages and lymphatic/blood vessels) were detected immunohistochemically. The median follow-up time was 6.0 years. High macrophage counts associated with a higher pT category and grade. Among patients undergoing transurethral resection, all studied markers apart from CLEVER-1/Stabilin-1 were associated with increased risk of progression and poorer disease-specific and overall survival in univariate analyses. High levels of two macrophage markers (CD68/MAC387(+/+) or CD68/CLEVER-1(+/+) groups) had an independent prognostic role after transurethral resection in multivariate analyses. In the cystectomy cohort, MAC387, alone and in combination with CD68, was associated with poorer survival in univariate analyses, but none of the markers were independent predictors of outcome in multivariate analyses. In conclusion, this study demonstrates that macrophage phenotypes provide significant independent prognostic information, particularly in bladder cancers undergoing transurethral resection. |
format | Online Article Text |
id | pubmed-4511010 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-45110102015-07-24 Tumor-Associated Macrophages Provide Significant Prognostic Information in Urothelial Bladder Cancer Boström, Minna M. Irjala, Heikki Mirtti, Tuomas Taimen, Pekka Kauko, Tommi Ålgars, Annika Jalkanen, Sirpa Boström, Peter J. PLoS One Research Article Inflammation is an important feature of carcinogenesis. Tumor-associated macrophages (TAMs) can be associated with either poor or improved prognosis, depending on their properties and polarization. Current knowledge of the prognostic significance of TAMs in bladder cancer is limited and was investigated in this study. We analyzed 184 urothelial bladder cancer patients undergoing transurethral resection of a bladder tumor or radical cystectomy. CD68 (pan-macrophage marker), MAC387 (polarized towards type 1 macrophages), and CLEVER-1/Stabilin-1 (type 2 macrophages and lymphatic/blood vessels) were detected immunohistochemically. The median follow-up time was 6.0 years. High macrophage counts associated with a higher pT category and grade. Among patients undergoing transurethral resection, all studied markers apart from CLEVER-1/Stabilin-1 were associated with increased risk of progression and poorer disease-specific and overall survival in univariate analyses. High levels of two macrophage markers (CD68/MAC387(+/+) or CD68/CLEVER-1(+/+) groups) had an independent prognostic role after transurethral resection in multivariate analyses. In the cystectomy cohort, MAC387, alone and in combination with CD68, was associated with poorer survival in univariate analyses, but none of the markers were independent predictors of outcome in multivariate analyses. In conclusion, this study demonstrates that macrophage phenotypes provide significant independent prognostic information, particularly in bladder cancers undergoing transurethral resection. Public Library of Science 2015-07-21 /pmc/articles/PMC4511010/ /pubmed/26197470 http://dx.doi.org/10.1371/journal.pone.0133552 Text en © 2015 Boström 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Boström, Minna M. Irjala, Heikki Mirtti, Tuomas Taimen, Pekka Kauko, Tommi Ålgars, Annika Jalkanen, Sirpa Boström, Peter J. Tumor-Associated Macrophages Provide Significant Prognostic Information in Urothelial Bladder Cancer |
title | Tumor-Associated Macrophages Provide Significant Prognostic Information in Urothelial Bladder Cancer |
title_full | Tumor-Associated Macrophages Provide Significant Prognostic Information in Urothelial Bladder Cancer |
title_fullStr | Tumor-Associated Macrophages Provide Significant Prognostic Information in Urothelial Bladder Cancer |
title_full_unstemmed | Tumor-Associated Macrophages Provide Significant Prognostic Information in Urothelial Bladder Cancer |
title_short | Tumor-Associated Macrophages Provide Significant Prognostic Information in Urothelial Bladder Cancer |
title_sort | tumor-associated macrophages provide significant prognostic information in urothelial bladder cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4511010/ https://www.ncbi.nlm.nih.gov/pubmed/26197470 http://dx.doi.org/10.1371/journal.pone.0133552 |
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