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B7-H3 expression in colorectal cancer: associations with clinicopathological parameters and patient outcome

BACKGROUND: We have previously reported overexpression of the immunoregulatory protein B7-H3 in colorectal cancer and that nuclear expression predicted poor outcome in colon cancer patients. The present study was performed to examine the prognostic role of B7-H3 in an independent colorectal cancer c...

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Autores principales: Ingebrigtsen, Vibeke A, Boye, Kjetil, Nesland, Jahn M, Nesbakken, Arild, Flatmark, Kjersti, Fodstad, Øystein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4148536/
https://www.ncbi.nlm.nih.gov/pubmed/25139714
http://dx.doi.org/10.1186/1471-2407-14-602
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author Ingebrigtsen, Vibeke A
Boye, Kjetil
Nesland, Jahn M
Nesbakken, Arild
Flatmark, Kjersti
Fodstad, Øystein
author_facet Ingebrigtsen, Vibeke A
Boye, Kjetil
Nesland, Jahn M
Nesbakken, Arild
Flatmark, Kjersti
Fodstad, Øystein
author_sort Ingebrigtsen, Vibeke A
collection PubMed
description BACKGROUND: We have previously reported overexpression of the immunoregulatory protein B7-H3 in colorectal cancer and that nuclear expression predicted poor outcome in colon cancer patients. The present study was performed to examine the prognostic role of B7-H3 in an independent colorectal cancer cohort. METHODS: Using tissue microarrays from 731 colorectal cancer patients, tumour B7-H3 expression was assessed by immunohistochemistry. Associations with clinicopathological parameters and patient outcome were investigated. RESULTS: Nuclear expression of B7-H3 in cancer cells was present in 27% of the samples in the total study cohort, while cytoplasmic/membrane and stromal expression was seen in 86% and 77% of the samples, respectively. Nuclear B7-H3 had no prognostic relevance in the complete outcome cohort, neither in colon cancer patients. However, nuclear B7-H3 was significantly associated with reduced recurrence-free survival in TNM stage I colorectal cancer patients. CONCLUSIONS: Overexpression of B7-H3 in colorectal cancer was confirmed, but in contrast to previous results, nuclear B7-H3 was not a strong prognostic biomarker in this cohort. The discrepancy might be related to the use of single-core tissue microarrays for detection of the heterogeneously expressed B7-H3, and the role of B7-H3 in colorectal cancer still needs further examination. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2407-14-602) contains supplementary material, which is available to authorized users.
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spelling pubmed-41485362014-08-29 B7-H3 expression in colorectal cancer: associations with clinicopathological parameters and patient outcome Ingebrigtsen, Vibeke A Boye, Kjetil Nesland, Jahn M Nesbakken, Arild Flatmark, Kjersti Fodstad, Øystein BMC Cancer Research Article BACKGROUND: We have previously reported overexpression of the immunoregulatory protein B7-H3 in colorectal cancer and that nuclear expression predicted poor outcome in colon cancer patients. The present study was performed to examine the prognostic role of B7-H3 in an independent colorectal cancer cohort. METHODS: Using tissue microarrays from 731 colorectal cancer patients, tumour B7-H3 expression was assessed by immunohistochemistry. Associations with clinicopathological parameters and patient outcome were investigated. RESULTS: Nuclear expression of B7-H3 in cancer cells was present in 27% of the samples in the total study cohort, while cytoplasmic/membrane and stromal expression was seen in 86% and 77% of the samples, respectively. Nuclear B7-H3 had no prognostic relevance in the complete outcome cohort, neither in colon cancer patients. However, nuclear B7-H3 was significantly associated with reduced recurrence-free survival in TNM stage I colorectal cancer patients. CONCLUSIONS: Overexpression of B7-H3 in colorectal cancer was confirmed, but in contrast to previous results, nuclear B7-H3 was not a strong prognostic biomarker in this cohort. The discrepancy might be related to the use of single-core tissue microarrays for detection of the heterogeneously expressed B7-H3, and the role of B7-H3 in colorectal cancer still needs further examination. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2407-14-602) contains supplementary material, which is available to authorized users. BioMed Central 2014-08-20 /pmc/articles/PMC4148536/ /pubmed/25139714 http://dx.doi.org/10.1186/1471-2407-14-602 Text en © Ingebrigtsen et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. 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 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 Article
Ingebrigtsen, Vibeke A
Boye, Kjetil
Nesland, Jahn M
Nesbakken, Arild
Flatmark, Kjersti
Fodstad, Øystein
B7-H3 expression in colorectal cancer: associations with clinicopathological parameters and patient outcome
title B7-H3 expression in colorectal cancer: associations with clinicopathological parameters and patient outcome
title_full B7-H3 expression in colorectal cancer: associations with clinicopathological parameters and patient outcome
title_fullStr B7-H3 expression in colorectal cancer: associations with clinicopathological parameters and patient outcome
title_full_unstemmed B7-H3 expression in colorectal cancer: associations with clinicopathological parameters and patient outcome
title_short B7-H3 expression in colorectal cancer: associations with clinicopathological parameters and patient outcome
title_sort b7-h3 expression in colorectal cancer: associations with clinicopathological parameters and patient outcome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4148536/
https://www.ncbi.nlm.nih.gov/pubmed/25139714
http://dx.doi.org/10.1186/1471-2407-14-602
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