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Expression and prognostic value of transcription factor PROX1 in colorectal cancer
BACKGROUND: PROX1 is a specific target of the β-catenin/TCF pathway in the intestinal epithelium. It acts as a regulator of progression from a benign to a highly dysplastic phenotype in colorectal tumours. However, the clinical significance of PROX1 expression is not known. METHODS: We studied the p...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3241535/ https://www.ncbi.nlm.nih.gov/pubmed/21970873 http://dx.doi.org/10.1038/bjc.2011.297 |
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author | Skog, M Bono, P Lundin, M Lundin, J Louhimo, J Linder, N Petrova, T V Andersson, L C Joensuu, H Alitalo, K Haglund, C H |
author_facet | Skog, M Bono, P Lundin, M Lundin, J Louhimo, J Linder, N Petrova, T V Andersson, L C Joensuu, H Alitalo, K Haglund, C H |
author_sort | Skog, M |
collection | PubMed |
description | BACKGROUND: PROX1 is a specific target of the β-catenin/TCF pathway in the intestinal epithelium. It acts as a regulator of progression from a benign to a highly dysplastic phenotype in colorectal tumours. However, the clinical significance of PROX1 expression is not known. METHODS: We studied the prognostic value of immunohistochemical expression of PROX1 in a series of 517 patients with colorectal cancer (CRC). RESULTS: The majority of the tumour samples expressed PROX1 (91%, 471 out of 517). High PROX1 expression was associated with a poor grade of tumour differentiation (P<0.0001). In the subgroup of patients with colon cancer, high PROX1 expression was associated with unfavourable colorectal cancer-specific survival (CCSS) as compared with low PROX1 expression (CCSS 47% vs 62% P=0.045; RR 1.47). The association between high PROX1 and poor outcome was further strengthened in female colon cancer patients (CCSS 38% vs 63% P=0.007; RR 2.02). Nonetheless, in multivariate survival analysis PROX1 expression was not retained as an independent prognostic factor. CONCLUSION: High PROX1 expression is associated with a poor grade of tumour differentiation, and, in colon cancer patients, also with less favourable patient outcome. Our results strengthen the previous preclinical observations that PROX1 has a role in tumour progression in CRC. |
format | Online Article Text |
id | pubmed-3241535 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-32415352012-10-25 Expression and prognostic value of transcription factor PROX1 in colorectal cancer Skog, M Bono, P Lundin, M Lundin, J Louhimo, J Linder, N Petrova, T V Andersson, L C Joensuu, H Alitalo, K Haglund, C H Br J Cancer Molecular Diagnostics BACKGROUND: PROX1 is a specific target of the β-catenin/TCF pathway in the intestinal epithelium. It acts as a regulator of progression from a benign to a highly dysplastic phenotype in colorectal tumours. However, the clinical significance of PROX1 expression is not known. METHODS: We studied the prognostic value of immunohistochemical expression of PROX1 in a series of 517 patients with colorectal cancer (CRC). RESULTS: The majority of the tumour samples expressed PROX1 (91%, 471 out of 517). High PROX1 expression was associated with a poor grade of tumour differentiation (P<0.0001). In the subgroup of patients with colon cancer, high PROX1 expression was associated with unfavourable colorectal cancer-specific survival (CCSS) as compared with low PROX1 expression (CCSS 47% vs 62% P=0.045; RR 1.47). The association between high PROX1 and poor outcome was further strengthened in female colon cancer patients (CCSS 38% vs 63% P=0.007; RR 2.02). Nonetheless, in multivariate survival analysis PROX1 expression was not retained as an independent prognostic factor. CONCLUSION: High PROX1 expression is associated with a poor grade of tumour differentiation, and, in colon cancer patients, also with less favourable patient outcome. Our results strengthen the previous preclinical observations that PROX1 has a role in tumour progression in CRC. Nature Publishing Group 2011-10-25 2011-10-04 /pmc/articles/PMC3241535/ /pubmed/21970873 http://dx.doi.org/10.1038/bjc.2011.297 Text en Copyright © 2011 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Molecular Diagnostics Skog, M Bono, P Lundin, M Lundin, J Louhimo, J Linder, N Petrova, T V Andersson, L C Joensuu, H Alitalo, K Haglund, C H Expression and prognostic value of transcription factor PROX1 in colorectal cancer |
title | Expression and prognostic value of transcription factor PROX1 in colorectal cancer |
title_full | Expression and prognostic value of transcription factor PROX1 in colorectal cancer |
title_fullStr | Expression and prognostic value of transcription factor PROX1 in colorectal cancer |
title_full_unstemmed | Expression and prognostic value of transcription factor PROX1 in colorectal cancer |
title_short | Expression and prognostic value of transcription factor PROX1 in colorectal cancer |
title_sort | expression and prognostic value of transcription factor prox1 in colorectal cancer |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3241535/ https://www.ncbi.nlm.nih.gov/pubmed/21970873 http://dx.doi.org/10.1038/bjc.2011.297 |
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