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Reduced expression of Axin correlates with tumour progression of oesophageal squamous cell carcinoma

Axin is a negative regulator of the Wnt signalling pathway, and genetic alterations of AXIN1 have been suggested to be an important factor of carcinogenesis in some tumours. The objective of this study was to clarify the clinicopathologic and prognostic significance of Axin in oesophageal squamous c...

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Autores principales: Nakajima, M, Fukuchi, M, Miyazaki, T, Masuda, N, Kato, H, Kuwano, H
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2377153/
https://www.ncbi.nlm.nih.gov/pubmed/12771989
http://dx.doi.org/10.1038/sj.bjc.6600941
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author Nakajima, M
Fukuchi, M
Miyazaki, T
Masuda, N
Kato, H
Kuwano, H
author_facet Nakajima, M
Fukuchi, M
Miyazaki, T
Masuda, N
Kato, H
Kuwano, H
author_sort Nakajima, M
collection PubMed
description Axin is a negative regulator of the Wnt signalling pathway, and genetic alterations of AXIN1 have been suggested to be an important factor of carcinogenesis in some tumours. The objective of this study was to clarify the clinicopathologic and prognostic significance of Axin in oesophageal squamous cell carcinoma (SCC). Immunohistochemical staining for Axin was performed on surgical specimens obtained from 81 patients with oesophageal SCC. Western and Northern blottings were performed on proteins and RNA from oesophageal SCC cell lines. Then polymerase chain reaction–single-strand conformational analysis (PCR–SSCP) was performed on DNA from oesophageal SCC patients and cell lines. Axin expression was found to be correlated inversely with depth of invasion, lymph node metastasis, and lymphatic invasion. Although univariate analysis showed Axin to be a negative predictor, multivariate analysis showed that it was not an independent prognostic marker. In all but one of the seven cell lines examined, the levels of protein expression were equivalent to RNA expression. PCR–SSCP showed that five patients and three cell lines had polymorphisms in exon 4 or 5 of the AXIN1 gene, but none of the 81 patients with oesophageal SCC had mutations. Our findings suggest that reduced expression of Axin is correlated with tumour progression of oesophageal SCC. However, additional studies will be necessary to elucidate the mechanism responsible for loss of Axin expression in tumour cells.
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spelling pubmed-23771532009-09-10 Reduced expression of Axin correlates with tumour progression of oesophageal squamous cell carcinoma Nakajima, M Fukuchi, M Miyazaki, T Masuda, N Kato, H Kuwano, H Br J Cancer Molecular and Cellular Pathology Axin is a negative regulator of the Wnt signalling pathway, and genetic alterations of AXIN1 have been suggested to be an important factor of carcinogenesis in some tumours. The objective of this study was to clarify the clinicopathologic and prognostic significance of Axin in oesophageal squamous cell carcinoma (SCC). Immunohistochemical staining for Axin was performed on surgical specimens obtained from 81 patients with oesophageal SCC. Western and Northern blottings were performed on proteins and RNA from oesophageal SCC cell lines. Then polymerase chain reaction–single-strand conformational analysis (PCR–SSCP) was performed on DNA from oesophageal SCC patients and cell lines. Axin expression was found to be correlated inversely with depth of invasion, lymph node metastasis, and lymphatic invasion. Although univariate analysis showed Axin to be a negative predictor, multivariate analysis showed that it was not an independent prognostic marker. In all but one of the seven cell lines examined, the levels of protein expression were equivalent to RNA expression. PCR–SSCP showed that five patients and three cell lines had polymorphisms in exon 4 or 5 of the AXIN1 gene, but none of the 81 patients with oesophageal SCC had mutations. Our findings suggest that reduced expression of Axin is correlated with tumour progression of oesophageal SCC. However, additional studies will be necessary to elucidate the mechanism responsible for loss of Axin expression in tumour cells. Nature Publishing Group 2003-06-02 2003-05-27 /pmc/articles/PMC2377153/ /pubmed/12771989 http://dx.doi.org/10.1038/sj.bjc.6600941 Text en Copyright © 2003 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 and Cellular Pathology
Nakajima, M
Fukuchi, M
Miyazaki, T
Masuda, N
Kato, H
Kuwano, H
Reduced expression of Axin correlates with tumour progression of oesophageal squamous cell carcinoma
title Reduced expression of Axin correlates with tumour progression of oesophageal squamous cell carcinoma
title_full Reduced expression of Axin correlates with tumour progression of oesophageal squamous cell carcinoma
title_fullStr Reduced expression of Axin correlates with tumour progression of oesophageal squamous cell carcinoma
title_full_unstemmed Reduced expression of Axin correlates with tumour progression of oesophageal squamous cell carcinoma
title_short Reduced expression of Axin correlates with tumour progression of oesophageal squamous cell carcinoma
title_sort reduced expression of axin correlates with tumour progression of oesophageal squamous cell carcinoma
topic Molecular and Cellular Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2377153/
https://www.ncbi.nlm.nih.gov/pubmed/12771989
http://dx.doi.org/10.1038/sj.bjc.6600941
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