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Quantitative evaluation of vimentin expression in tumour stroma of colorectal cancer
Recent studies have identified vimentin, a type III intermediate filament, among genes differentially expressed in tumours with more invasive features, suggesting an association between vimentin and tumour progression. The aim of this study, was to investigate whether vimentin expression in colon ca...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360104/ https://www.ncbi.nlm.nih.gov/pubmed/17325702 http://dx.doi.org/10.1038/sj.bjc.6603651 |
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author | Ngan, C Y Yamamoto, H Seshimo, I Tsujino, T Man-i, M Ikeda, J-I Konishi, K Takemasa, I Ikeda, M Sekimoto, M Matsuura, N Monden, M |
author_facet | Ngan, C Y Yamamoto, H Seshimo, I Tsujino, T Man-i, M Ikeda, J-I Konishi, K Takemasa, I Ikeda, M Sekimoto, M Matsuura, N Monden, M |
author_sort | Ngan, C Y |
collection | PubMed |
description | Recent studies have identified vimentin, a type III intermediate filament, among genes differentially expressed in tumours with more invasive features, suggesting an association between vimentin and tumour progression. The aim of this study, was to investigate whether vimentin expression in colon cancer tissue is of clinical relevance. We performed immunostaining in 142 colorectal cancer (CRC) samples and quantified the amount of vimentin expression using computer-assisted image analysis. Vimentin expression in the tumour stroma of CRC was associated with shorter survival. Overall survival in the high vimentin expression group was 71.2% compared with 90.4% in the low-expression group (P=0.002), whereas disease-free survival for the high-expression group was 62.7% compared with 86.7% for the low-expression group (P=0.001). Furthermore, the prognostic power of vimentin for disease recurrence was maintained in both stage II and III CRC. Multivariate analysis suggested that vimentin was a better prognostic indicator for disease recurrence (risk ratio=3.5) than the widely used lymph node status (risk ratio=2.2). Vimentin expression in the tumour stroma may reflect a higher malignant potential of the tumour and may be a useful predictive marker for disease recurrence in CRC patients. |
format | Text |
id | pubmed-2360104 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23601042009-09-10 Quantitative evaluation of vimentin expression in tumour stroma of colorectal cancer Ngan, C Y Yamamoto, H Seshimo, I Tsujino, T Man-i, M Ikeda, J-I Konishi, K Takemasa, I Ikeda, M Sekimoto, M Matsuura, N Monden, M Br J Cancer Molecular Diagnostics Recent studies have identified vimentin, a type III intermediate filament, among genes differentially expressed in tumours with more invasive features, suggesting an association between vimentin and tumour progression. The aim of this study, was to investigate whether vimentin expression in colon cancer tissue is of clinical relevance. We performed immunostaining in 142 colorectal cancer (CRC) samples and quantified the amount of vimentin expression using computer-assisted image analysis. Vimentin expression in the tumour stroma of CRC was associated with shorter survival. Overall survival in the high vimentin expression group was 71.2% compared with 90.4% in the low-expression group (P=0.002), whereas disease-free survival for the high-expression group was 62.7% compared with 86.7% for the low-expression group (P=0.001). Furthermore, the prognostic power of vimentin for disease recurrence was maintained in both stage II and III CRC. Multivariate analysis suggested that vimentin was a better prognostic indicator for disease recurrence (risk ratio=3.5) than the widely used lymph node status (risk ratio=2.2). Vimentin expression in the tumour stroma may reflect a higher malignant potential of the tumour and may be a useful predictive marker for disease recurrence in CRC patients. Nature Publishing Group 2007-03-26 2007-02-27 /pmc/articles/PMC2360104/ /pubmed/17325702 http://dx.doi.org/10.1038/sj.bjc.6603651 Text en Copyright © 2007 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 Ngan, C Y Yamamoto, H Seshimo, I Tsujino, T Man-i, M Ikeda, J-I Konishi, K Takemasa, I Ikeda, M Sekimoto, M Matsuura, N Monden, M Quantitative evaluation of vimentin expression in tumour stroma of colorectal cancer |
title | Quantitative evaluation of vimentin expression in tumour stroma of colorectal cancer |
title_full | Quantitative evaluation of vimentin expression in tumour stroma of colorectal cancer |
title_fullStr | Quantitative evaluation of vimentin expression in tumour stroma of colorectal cancer |
title_full_unstemmed | Quantitative evaluation of vimentin expression in tumour stroma of colorectal cancer |
title_short | Quantitative evaluation of vimentin expression in tumour stroma of colorectal cancer |
title_sort | quantitative evaluation of vimentin expression in tumour stroma of colorectal cancer |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2360104/ https://www.ncbi.nlm.nih.gov/pubmed/17325702 http://dx.doi.org/10.1038/sj.bjc.6603651 |
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