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High intratumoral expression of fibroblast activation protein (FAP) in colon cancer is associated with poorer patient prognosis
-An active stroma is important for cancer cell invasion and metastasis. We investigated the expression of fibroblast activation protein (FAP) in relation to patient prognosis in colorectal cancer. Colorectal cancer specimens from 449 patients were immunohistochemically stained with a FAP antibody an...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3597266/ https://www.ncbi.nlm.nih.gov/pubmed/23328994 http://dx.doi.org/10.1007/s13277-012-0638-2 |
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author | Wikberg, Maria L. Edin, Sofia Lundberg, Ida V. Van Guelpen, Bethany Dahlin, Anna M. Rutegård, Jörgen Stenling, Roger Öberg, Åke Palmqvist, Richard |
author_facet | Wikberg, Maria L. Edin, Sofia Lundberg, Ida V. Van Guelpen, Bethany Dahlin, Anna M. Rutegård, Jörgen Stenling, Roger Öberg, Åke Palmqvist, Richard |
author_sort | Wikberg, Maria L. |
collection | PubMed |
description | -An active stroma is important for cancer cell invasion and metastasis. We investigated the expression of fibroblast activation protein (FAP) in relation to patient prognosis in colorectal cancer. Colorectal cancer specimens from 449 patients were immunohistochemically stained with a FAP antibody and evaluated in the tumor center and tumor front using a semiquantitative four-level scale. FAP was expressed by fibroblasts in 85–90 % of the tumors examined. High versus no/low expression in the tumor center was associated with poor prognosis (multivariate hazard ratio, HR = 1.72; 95 % CI 1.07–2.77, p = 0.025). FAP expression in the tumor front, though more frequent than in the tumor center, was not associated with prognosis. FAP expression in the tumor center was more common in specimens with positive microsatellite instability (MSI) screening status and in patients with high CpG island methylator phenotype (CIMP) status. However, inclusion of MSI screening status and CIMP status in the multivariate analysis strengthened the risk estimates for high FAP expression in the tumor center (HR = 1.89; 95 % CI 1.13–3.14; p = 0.014), emphasizing the role of FAP as an independent prognostic factor. Stromal FAP expression is common in colorectal cancer, and we conclude that high FAP expression in the tumor center, but not the tumor front, is an independent negative prognostic factor. |
format | Online Article Text |
id | pubmed-3597266 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-35972662013-03-15 High intratumoral expression of fibroblast activation protein (FAP) in colon cancer is associated with poorer patient prognosis Wikberg, Maria L. Edin, Sofia Lundberg, Ida V. Van Guelpen, Bethany Dahlin, Anna M. Rutegård, Jörgen Stenling, Roger Öberg, Åke Palmqvist, Richard Tumour Biol Research Article -An active stroma is important for cancer cell invasion and metastasis. We investigated the expression of fibroblast activation protein (FAP) in relation to patient prognosis in colorectal cancer. Colorectal cancer specimens from 449 patients were immunohistochemically stained with a FAP antibody and evaluated in the tumor center and tumor front using a semiquantitative four-level scale. FAP was expressed by fibroblasts in 85–90 % of the tumors examined. High versus no/low expression in the tumor center was associated with poor prognosis (multivariate hazard ratio, HR = 1.72; 95 % CI 1.07–2.77, p = 0.025). FAP expression in the tumor front, though more frequent than in the tumor center, was not associated with prognosis. FAP expression in the tumor center was more common in specimens with positive microsatellite instability (MSI) screening status and in patients with high CpG island methylator phenotype (CIMP) status. However, inclusion of MSI screening status and CIMP status in the multivariate analysis strengthened the risk estimates for high FAP expression in the tumor center (HR = 1.89; 95 % CI 1.13–3.14; p = 0.014), emphasizing the role of FAP as an independent prognostic factor. Stromal FAP expression is common in colorectal cancer, and we conclude that high FAP expression in the tumor center, but not the tumor front, is an independent negative prognostic factor. Springer Netherlands 2013-01-18 /pmc/articles/PMC3597266/ /pubmed/23328994 http://dx.doi.org/10.1007/s13277-012-0638-2 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by-nc/2.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Research Article Wikberg, Maria L. Edin, Sofia Lundberg, Ida V. Van Guelpen, Bethany Dahlin, Anna M. Rutegård, Jörgen Stenling, Roger Öberg, Åke Palmqvist, Richard High intratumoral expression of fibroblast activation protein (FAP) in colon cancer is associated with poorer patient prognosis |
title | High intratumoral expression of fibroblast activation protein (FAP) in colon cancer is associated with poorer patient prognosis |
title_full | High intratumoral expression of fibroblast activation protein (FAP) in colon cancer is associated with poorer patient prognosis |
title_fullStr | High intratumoral expression of fibroblast activation protein (FAP) in colon cancer is associated with poorer patient prognosis |
title_full_unstemmed | High intratumoral expression of fibroblast activation protein (FAP) in colon cancer is associated with poorer patient prognosis |
title_short | High intratumoral expression of fibroblast activation protein (FAP) in colon cancer is associated with poorer patient prognosis |
title_sort | high intratumoral expression of fibroblast activation protein (fap) in colon cancer is associated with poorer patient prognosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3597266/ https://www.ncbi.nlm.nih.gov/pubmed/23328994 http://dx.doi.org/10.1007/s13277-012-0638-2 |
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