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Expression of nm23-H1 gene product in esophageal squamous cell carcinoma and its association with vessel invasion and survival
BACKGROUND: We assessed the nm23-H1 gene product expression and its relationship with lymphatic and blood vessel invasion in patients with esophageal squamous cell carcinoma. METHODS: Formalin-fixed and paraffin-embedded tissue sections from 45 patients who were treated surgically were used in this...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2001
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC32171/ https://www.ncbi.nlm.nih.gov/pubmed/11319942 http://dx.doi.org/10.1186/1471-2407-1-3 |
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author | Tomita, Masaki Ayabe, Takanori Matsuzaki, Yasunori Edagawa, Masao Maeda, Masayuki Shimizu, Tetsuya Hara, Masaki Onitsuka, Toshio |
author_facet | Tomita, Masaki Ayabe, Takanori Matsuzaki, Yasunori Edagawa, Masao Maeda, Masayuki Shimizu, Tetsuya Hara, Masaki Onitsuka, Toshio |
author_sort | Tomita, Masaki |
collection | PubMed |
description | BACKGROUND: We assessed the nm23-H1 gene product expression and its relationship with lymphatic and blood vessel invasion in patients with esophageal squamous cell carcinoma. METHODS: Formalin-fixed and paraffin-embedded tissue sections from 45 patients who were treated surgically were used in this study. Pathologists graded lymphatic and blood vessel invasion in each of the tissue samples. Expression of nm23-Hl gene product was determined using a specific monoclonal antibody. RESULTS: Expression of nm23-H1 gene product was present in 17 (37.8%) cases. We found an inverse correlation between nm23-H1 gene product expression and lymphatic vessel invasion, whereas no correlation between nm23-H1 gene product expression and blood vessel invasion. Overall survival rate was not different between nm23-H1 gene product positive and negative patients (p = 0.21). However, reduced expression of nm23-H1 gene product was associated with shorter overall survival in patients with involved lymph nodes (p < 0.05), but not in patients without involved lymph nodes (p = 0.87). CONCLUSIONS: In patients with esophageal squamous cell carcinoma, there appears to be an inverse relationship between nm23-H1 gene product expression and lymphatic vessel invasion. Furthermore, nm23-H1 gene product expression might be a prognostic marker in patients with involved lymph nodes. Our data does not demonstrate any correlation between nm23-H1 gene product expression and blood vessel invasion. |
format | Text |
id | pubmed-32171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2001 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-321712001-06-01 Expression of nm23-H1 gene product in esophageal squamous cell carcinoma and its association with vessel invasion and survival Tomita, Masaki Ayabe, Takanori Matsuzaki, Yasunori Edagawa, Masao Maeda, Masayuki Shimizu, Tetsuya Hara, Masaki Onitsuka, Toshio BMC Cancer Research Article BACKGROUND: We assessed the nm23-H1 gene product expression and its relationship with lymphatic and blood vessel invasion in patients with esophageal squamous cell carcinoma. METHODS: Formalin-fixed and paraffin-embedded tissue sections from 45 patients who were treated surgically were used in this study. Pathologists graded lymphatic and blood vessel invasion in each of the tissue samples. Expression of nm23-Hl gene product was determined using a specific monoclonal antibody. RESULTS: Expression of nm23-H1 gene product was present in 17 (37.8%) cases. We found an inverse correlation between nm23-H1 gene product expression and lymphatic vessel invasion, whereas no correlation between nm23-H1 gene product expression and blood vessel invasion. Overall survival rate was not different between nm23-H1 gene product positive and negative patients (p = 0.21). However, reduced expression of nm23-H1 gene product was associated with shorter overall survival in patients with involved lymph nodes (p < 0.05), but not in patients without involved lymph nodes (p = 0.87). CONCLUSIONS: In patients with esophageal squamous cell carcinoma, there appears to be an inverse relationship between nm23-H1 gene product expression and lymphatic vessel invasion. Furthermore, nm23-H1 gene product expression might be a prognostic marker in patients with involved lymph nodes. Our data does not demonstrate any correlation between nm23-H1 gene product expression and blood vessel invasion. BioMed Central 2001-04-19 /pmc/articles/PMC32171/ /pubmed/11319942 http://dx.doi.org/10.1186/1471-2407-1-3 Text en Copyright © 2001 Tomita et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. |
spellingShingle | Research Article Tomita, Masaki Ayabe, Takanori Matsuzaki, Yasunori Edagawa, Masao Maeda, Masayuki Shimizu, Tetsuya Hara, Masaki Onitsuka, Toshio Expression of nm23-H1 gene product in esophageal squamous cell carcinoma and its association with vessel invasion and survival |
title | Expression of nm23-H1 gene product in esophageal squamous cell carcinoma and its association with vessel invasion and survival |
title_full | Expression of nm23-H1 gene product in esophageal squamous cell carcinoma and its association with vessel invasion and survival |
title_fullStr | Expression of nm23-H1 gene product in esophageal squamous cell carcinoma and its association with vessel invasion and survival |
title_full_unstemmed | Expression of nm23-H1 gene product in esophageal squamous cell carcinoma and its association with vessel invasion and survival |
title_short | Expression of nm23-H1 gene product in esophageal squamous cell carcinoma and its association with vessel invasion and survival |
title_sort | expression of nm23-h1 gene product in esophageal squamous cell carcinoma and its association with vessel invasion and survival |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC32171/ https://www.ncbi.nlm.nih.gov/pubmed/11319942 http://dx.doi.org/10.1186/1471-2407-1-3 |
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