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Slug expression is an independent prognostic parameter for poor survival in colorectal carcinoma patients

Slug, a member of the Snail family of transcription factors, plays a crucial role in the regulation of epithelial-mesenchymal transition (EMT) by suppressing several epithelial markers and adhesion molecules including E-cadherin. Recently, several studies have reported Slug to be expressed in breast...

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Autores principales: Shioiri, M, Shida, T, Koda, K, Oda, K, Seike, K, Nishimura, M, Takano, S, Miyazaki, M
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361350/
https://www.ncbi.nlm.nih.gov/pubmed/16773075
http://dx.doi.org/10.1038/sj.bjc.6603193
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author Shioiri, M
Shida, T
Koda, K
Oda, K
Seike, K
Nishimura, M
Takano, S
Miyazaki, M
author_facet Shioiri, M
Shida, T
Koda, K
Oda, K
Seike, K
Nishimura, M
Takano, S
Miyazaki, M
author_sort Shioiri, M
collection PubMed
description Slug, a member of the Snail family of transcription factors, plays a crucial role in the regulation of epithelial-mesenchymal transition (EMT) by suppressing several epithelial markers and adhesion molecules including E-cadherin. Recently, several studies have reported Slug to be expressed in breast carcinoma, oesophageal carcinoma accompanied with shorter survival. In this study, we first investigated expression of Slug mRNA in five colorectal carcinoma cell lines by reverse transcription–polymerase chain reaction. Furthermore, we investigated Slug and E-cadherin expression by immunohistochemistry in 138 patients with colorectal carcinoma. Slug mRNA was clearly expressed in four out of five colorectal carcinoma cell lines. Positive expression of Slug and E-cadherin was observed in 37 and 58% of cases, respectively. The positive expression of Slug was significantly associated with Dukes stage and distant metastasis (P=0.0027 and 0.0007), and the positive expression of Slug had a significant impact on patient overall survival (P<0.0001, log-rank test). Moreover, patients with positive expression of Slug and reduced expression of E-cadherin showed the worst prognosis (P<0.0001, log-rank test). Multivariate analysis indicated that Slug expression was an independent prognostic factor. These results suggest that positive Slug expression in colorectal carcinoma patients may become a significant parameter of poor prognosis.
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spelling pubmed-23613502009-09-10 Slug expression is an independent prognostic parameter for poor survival in colorectal carcinoma patients Shioiri, M Shida, T Koda, K Oda, K Seike, K Nishimura, M Takano, S Miyazaki, M Br J Cancer Clinical Study Slug, a member of the Snail family of transcription factors, plays a crucial role in the regulation of epithelial-mesenchymal transition (EMT) by suppressing several epithelial markers and adhesion molecules including E-cadherin. Recently, several studies have reported Slug to be expressed in breast carcinoma, oesophageal carcinoma accompanied with shorter survival. In this study, we first investigated expression of Slug mRNA in five colorectal carcinoma cell lines by reverse transcription–polymerase chain reaction. Furthermore, we investigated Slug and E-cadherin expression by immunohistochemistry in 138 patients with colorectal carcinoma. Slug mRNA was clearly expressed in four out of five colorectal carcinoma cell lines. Positive expression of Slug and E-cadherin was observed in 37 and 58% of cases, respectively. The positive expression of Slug was significantly associated with Dukes stage and distant metastasis (P=0.0027 and 0.0007), and the positive expression of Slug had a significant impact on patient overall survival (P<0.0001, log-rank test). Moreover, patients with positive expression of Slug and reduced expression of E-cadherin showed the worst prognosis (P<0.0001, log-rank test). Multivariate analysis indicated that Slug expression was an independent prognostic factor. These results suggest that positive Slug expression in colorectal carcinoma patients may become a significant parameter of poor prognosis. Nature Publishing Group 2006-06-19 2006-06-13 /pmc/articles/PMC2361350/ /pubmed/16773075 http://dx.doi.org/10.1038/sj.bjc.6603193 Text en Copyright © 2006 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 Clinical Study
Shioiri, M
Shida, T
Koda, K
Oda, K
Seike, K
Nishimura, M
Takano, S
Miyazaki, M
Slug expression is an independent prognostic parameter for poor survival in colorectal carcinoma patients
title Slug expression is an independent prognostic parameter for poor survival in colorectal carcinoma patients
title_full Slug expression is an independent prognostic parameter for poor survival in colorectal carcinoma patients
title_fullStr Slug expression is an independent prognostic parameter for poor survival in colorectal carcinoma patients
title_full_unstemmed Slug expression is an independent prognostic parameter for poor survival in colorectal carcinoma patients
title_short Slug expression is an independent prognostic parameter for poor survival in colorectal carcinoma patients
title_sort slug expression is an independent prognostic parameter for poor survival in colorectal carcinoma patients
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361350/
https://www.ncbi.nlm.nih.gov/pubmed/16773075
http://dx.doi.org/10.1038/sj.bjc.6603193
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