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Low E-cadherin expression in bladder cancer at the transcriptional and protein level provides prognostic information
We studied E-cadherin down-regulation at the protein level in frozen sections of 111 bladder tumours and 13 normal bladder specimens by means of immunohistochemistry, and at the mRNA level by semi-quantitative RT-PCR in 40 of the same tumours. Results indicate that E-cadherin expression detected by...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2000
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363483/ https://www.ncbi.nlm.nih.gov/pubmed/10901372 http://dx.doi.org/10.1054/bjoc.2000.1233 |
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author | Popov, Z Medina, S Gil-Diez de Lefrere-Belda, M-A Hoznek, A Bastuji-Garin, S Abbou, C C Thiery, J P Radvanyi, F Chopin, D K |
author_facet | Popov, Z Medina, S Gil-Diez de Lefrere-Belda, M-A Hoznek, A Bastuji-Garin, S Abbou, C C Thiery, J P Radvanyi, F Chopin, D K |
author_sort | Popov, Z |
collection | PubMed |
description | We studied E-cadherin down-regulation at the protein level in frozen sections of 111 bladder tumours and 13 normal bladder specimens by means of immunohistochemistry, and at the mRNA level by semi-quantitative RT-PCR in 40 of the same tumours. Results indicate that E-cadherin expression detected by immunohistochemistry correlated with both stage and grade (P< 0.0001 and P< 0.001, respectively). Analysis of recurrence, progression and survival over a mean period of 36 months after surgery in the entire cohort showed that abnormal E-cadherin immunoreactivity correlated strongly with poor outcome (log-rank test: P = 0.001, P = 0.0001 and P = 0.0003, respectively). In multistep logistic regression analysis, only E-cadherin status and stage had significant additional prognostic value (P = 0.008 and OR = 0.2;P = 0.03 and OR = 3.6, respectively). Survival estimates derived from RT-PCR transcript quantification differed significantly for low and high expression (log-rank test: P = 0.0006). These results suggest that the alteration occurs at the transcriptional level and support the clinical and biological relevance of cell adhesion molecules in bladder cancer. © 2000 Cancer Research Campaign |
format | Text |
id | pubmed-2363483 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23634832009-09-10 Low E-cadherin expression in bladder cancer at the transcriptional and protein level provides prognostic information Popov, Z Medina, S Gil-Diez de Lefrere-Belda, M-A Hoznek, A Bastuji-Garin, S Abbou, C C Thiery, J P Radvanyi, F Chopin, D K Br J Cancer Regular Article We studied E-cadherin down-regulation at the protein level in frozen sections of 111 bladder tumours and 13 normal bladder specimens by means of immunohistochemistry, and at the mRNA level by semi-quantitative RT-PCR in 40 of the same tumours. Results indicate that E-cadherin expression detected by immunohistochemistry correlated with both stage and grade (P< 0.0001 and P< 0.001, respectively). Analysis of recurrence, progression and survival over a mean period of 36 months after surgery in the entire cohort showed that abnormal E-cadherin immunoreactivity correlated strongly with poor outcome (log-rank test: P = 0.001, P = 0.0001 and P = 0.0003, respectively). In multistep logistic regression analysis, only E-cadherin status and stage had significant additional prognostic value (P = 0.008 and OR = 0.2;P = 0.03 and OR = 3.6, respectively). Survival estimates derived from RT-PCR transcript quantification differed significantly for low and high expression (log-rank test: P = 0.0006). These results suggest that the alteration occurs at the transcriptional level and support the clinical and biological relevance of cell adhesion molecules in bladder cancer. © 2000 Cancer Research Campaign Nature Publishing Group 2000-07 2000-06-15 /pmc/articles/PMC2363483/ /pubmed/10901372 http://dx.doi.org/10.1054/bjoc.2000.1233 Text en Copyright © 2000 Cancer Research Campaign 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 | Regular Article Popov, Z Medina, S Gil-Diez de Lefrere-Belda, M-A Hoznek, A Bastuji-Garin, S Abbou, C C Thiery, J P Radvanyi, F Chopin, D K Low E-cadherin expression in bladder cancer at the transcriptional and protein level provides prognostic information |
title | Low E-cadherin expression in bladder cancer at the transcriptional and protein level provides prognostic information |
title_full | Low E-cadherin expression in bladder cancer at the transcriptional and protein level provides prognostic information |
title_fullStr | Low E-cadherin expression in bladder cancer at the transcriptional and protein level provides prognostic information |
title_full_unstemmed | Low E-cadherin expression in bladder cancer at the transcriptional and protein level provides prognostic information |
title_short | Low E-cadherin expression in bladder cancer at the transcriptional and protein level provides prognostic information |
title_sort | low e-cadherin expression in bladder cancer at the transcriptional and protein level provides prognostic information |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363483/ https://www.ncbi.nlm.nih.gov/pubmed/10901372 http://dx.doi.org/10.1054/bjoc.2000.1233 |
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