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Factors that contribute to faecal cyclooxygenase-2 mRNA expression in subjects with colorectal cancer
BACKGROUND: We previously reported that a faecal cyclooxygenase-2 (COX-2) mRNA assay was useful for identifying colorectal cancer (CRC). This study sought to investigate the factors that contribute to faecal COX-2 mRNA expression in subjects with CRC. METHODS: The study cohort comprised 78 patients...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2833255/ https://www.ncbi.nlm.nih.gov/pubmed/20145612 http://dx.doi.org/10.1038/sj.bjc.6605564 |
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author | Hamaya, Y Yoshida, K Takai, T Ikuma, M Hishida, A Kanaoka, S |
author_facet | Hamaya, Y Yoshida, K Takai, T Ikuma, M Hishida, A Kanaoka, S |
author_sort | Hamaya, Y |
collection | PubMed |
description | BACKGROUND: We previously reported that a faecal cyclooxygenase-2 (COX-2) mRNA assay was useful for identifying colorectal cancer (CRC). This study sought to investigate the factors that contribute to faecal COX-2 mRNA expression in subjects with CRC. METHODS: The study cohort comprised 78 patients with CRC and 36 control subjects. The expressions of COX-2, β-2-microglobulin (B2M), carcinoembryonic antigen (CEA), E-cadherin (E-cad), and CD45 mRNA in faeces and COX-2 mRNA expression in tissue were determined by quantitative real-time RT–PCR. RESULTS: The level of faecal expression of COX-2 mRNA in CRC was significantly higher than that in controls. A significant correlation was found between faecal COX-2 mRNA expression and faecal B2M, CEA, E-cad, or CD45 mRNAs, markers of exfoliated total cells, colonocytes, and leukocytes, respectively. A significant correlation was found between the expression of COX-2 mRNA in faeces and tumour surface area, COX-2 mRNA expression in primary tumour. There was no difference in faecal COX-2 mRNA expression between proximal CRC and distal CRC. CONCLUSION: COX-2 mRNA expression in faeces seems to originate from tumour lesion and to be affected by factors such as the number of exfoliated cells, exfoliation of inflammatory cells, COX-2 mRNA expression in tumour, and tumour size. |
format | Text |
id | pubmed-2833255 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-28332552011-03-02 Factors that contribute to faecal cyclooxygenase-2 mRNA expression in subjects with colorectal cancer Hamaya, Y Yoshida, K Takai, T Ikuma, M Hishida, A Kanaoka, S Br J Cancer Molecular Diagnostics BACKGROUND: We previously reported that a faecal cyclooxygenase-2 (COX-2) mRNA assay was useful for identifying colorectal cancer (CRC). This study sought to investigate the factors that contribute to faecal COX-2 mRNA expression in subjects with CRC. METHODS: The study cohort comprised 78 patients with CRC and 36 control subjects. The expressions of COX-2, β-2-microglobulin (B2M), carcinoembryonic antigen (CEA), E-cadherin (E-cad), and CD45 mRNA in faeces and COX-2 mRNA expression in tissue were determined by quantitative real-time RT–PCR. RESULTS: The level of faecal expression of COX-2 mRNA in CRC was significantly higher than that in controls. A significant correlation was found between faecal COX-2 mRNA expression and faecal B2M, CEA, E-cad, or CD45 mRNAs, markers of exfoliated total cells, colonocytes, and leukocytes, respectively. A significant correlation was found between the expression of COX-2 mRNA in faeces and tumour surface area, COX-2 mRNA expression in primary tumour. There was no difference in faecal COX-2 mRNA expression between proximal CRC and distal CRC. CONCLUSION: COX-2 mRNA expression in faeces seems to originate from tumour lesion and to be affected by factors such as the number of exfoliated cells, exfoliation of inflammatory cells, COX-2 mRNA expression in tumour, and tumour size. Nature Publishing Group 2010-03-02 2010-02-09 /pmc/articles/PMC2833255/ /pubmed/20145612 http://dx.doi.org/10.1038/sj.bjc.6605564 Text en Copyright © 2010 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 Diagnostics Hamaya, Y Yoshida, K Takai, T Ikuma, M Hishida, A Kanaoka, S Factors that contribute to faecal cyclooxygenase-2 mRNA expression in subjects with colorectal cancer |
title | Factors that contribute to faecal cyclooxygenase-2 mRNA expression in subjects with colorectal cancer |
title_full | Factors that contribute to faecal cyclooxygenase-2 mRNA expression in subjects with colorectal cancer |
title_fullStr | Factors that contribute to faecal cyclooxygenase-2 mRNA expression in subjects with colorectal cancer |
title_full_unstemmed | Factors that contribute to faecal cyclooxygenase-2 mRNA expression in subjects with colorectal cancer |
title_short | Factors that contribute to faecal cyclooxygenase-2 mRNA expression in subjects with colorectal cancer |
title_sort | factors that contribute to faecal cyclooxygenase-2 mrna expression in subjects with colorectal cancer |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2833255/ https://www.ncbi.nlm.nih.gov/pubmed/20145612 http://dx.doi.org/10.1038/sj.bjc.6605564 |
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