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Clinicopathological and prognostic significance of HER-2/neu and VEGF expression in colon carcinomas
BACKGROUND: HER-2/neu and VEGF expression is correlated with disease behaviors in various cancers. However, evidence for their expression in colon cancer is rather contradictory both for the protein expression status and prognostic value. HER-2/neu is found to participate in VEGF regulation, and has...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3144457/ https://www.ncbi.nlm.nih.gov/pubmed/21708009 http://dx.doi.org/10.1186/1471-2407-11-277 |
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author | Li, Qingguo Wang, Daorong Li, Jing Chen, Ping |
author_facet | Li, Qingguo Wang, Daorong Li, Jing Chen, Ping |
author_sort | Li, Qingguo |
collection | PubMed |
description | BACKGROUND: HER-2/neu and VEGF expression is correlated with disease behaviors in various cancers. However, evidence for their expression in colon cancer is rather contradictory both for the protein expression status and prognostic value. HER-2/neu is found to participate in VEGF regulation, and has known correlation with VEGF expression in some tumors. In this study, we investigated HER-2/neu and VEGF expression in Chinese colon patients and explored whether there was any correlation between their expression patterns. METHODS: HER-2/neu and VEGF were investigated immunohistochemically using tumor samples obtained from 317 colon cancer patients with all tumor stages. Correlation of the degree of staining with clinicopathological parameters and survival was investigated. RESULTS: Positive expression rates of HER-2/neu and VEGF in colon cancer were 15.5% and 55.5% respectively. HER-2/neu expression was significantly correlated with tumor size and distant metastases (P < 0.05), but was not an independent prognostic marker of survival (P > 0.05). Expression of VEGF was significantly correlated with tumor size, tumor stage, lymph node metastases, and distant metastases (P < 0.05). The 5-year survival rate in patients with negative and positive VEGF expression was 70.2% and 61.9% respectively; the difference was not statistically significant (P = 0.146). No correlation between HER-2/neu and VEGF expression was detected (P = 0.151). CONCLUSIONS: HER-2/neu and VEGF are not important prognostic markers of colon cancer. The present results do not support any association between HER2/neu and VEGF expression in this setting. |
format | Online Article Text |
id | pubmed-3144457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31444572011-07-28 Clinicopathological and prognostic significance of HER-2/neu and VEGF expression in colon carcinomas Li, Qingguo Wang, Daorong Li, Jing Chen, Ping BMC Cancer Research Article BACKGROUND: HER-2/neu and VEGF expression is correlated with disease behaviors in various cancers. However, evidence for their expression in colon cancer is rather contradictory both for the protein expression status and prognostic value. HER-2/neu is found to participate in VEGF regulation, and has known correlation with VEGF expression in some tumors. In this study, we investigated HER-2/neu and VEGF expression in Chinese colon patients and explored whether there was any correlation between their expression patterns. METHODS: HER-2/neu and VEGF were investigated immunohistochemically using tumor samples obtained from 317 colon cancer patients with all tumor stages. Correlation of the degree of staining with clinicopathological parameters and survival was investigated. RESULTS: Positive expression rates of HER-2/neu and VEGF in colon cancer were 15.5% and 55.5% respectively. HER-2/neu expression was significantly correlated with tumor size and distant metastases (P < 0.05), but was not an independent prognostic marker of survival (P > 0.05). Expression of VEGF was significantly correlated with tumor size, tumor stage, lymph node metastases, and distant metastases (P < 0.05). The 5-year survival rate in patients with negative and positive VEGF expression was 70.2% and 61.9% respectively; the difference was not statistically significant (P = 0.146). No correlation between HER-2/neu and VEGF expression was detected (P = 0.151). CONCLUSIONS: HER-2/neu and VEGF are not important prognostic markers of colon cancer. The present results do not support any association between HER2/neu and VEGF expression in this setting. BioMed Central 2011-06-27 /pmc/articles/PMC3144457/ /pubmed/21708009 http://dx.doi.org/10.1186/1471-2407-11-277 Text en Copyright ©2011 Li et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 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 cited. |
spellingShingle | Research Article Li, Qingguo Wang, Daorong Li, Jing Chen, Ping Clinicopathological and prognostic significance of HER-2/neu and VEGF expression in colon carcinomas |
title | Clinicopathological and prognostic significance of HER-2/neu and VEGF expression in colon carcinomas |
title_full | Clinicopathological and prognostic significance of HER-2/neu and VEGF expression in colon carcinomas |
title_fullStr | Clinicopathological and prognostic significance of HER-2/neu and VEGF expression in colon carcinomas |
title_full_unstemmed | Clinicopathological and prognostic significance of HER-2/neu and VEGF expression in colon carcinomas |
title_short | Clinicopathological and prognostic significance of HER-2/neu and VEGF expression in colon carcinomas |
title_sort | clinicopathological and prognostic significance of her-2/neu and vegf expression in colon carcinomas |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3144457/ https://www.ncbi.nlm.nih.gov/pubmed/21708009 http://dx.doi.org/10.1186/1471-2407-11-277 |
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