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Expression of D-type cyclins in colon cancer and in cell lines from colon carcinomas
Cyclins D1, D2 and D3 play important roles in cell proliferation and differentiation. Although their abnormal expression has been linked to cancer development and progression in a number of tissues, the expression of cyclin D2 and D3 proteins in colon cancer has not yet been characterised. In this s...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2005
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361572/ https://www.ncbi.nlm.nih.gov/pubmed/16012517 http://dx.doi.org/10.1038/sj.bjc.6602709 |
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author | Mermelshtein, A Gerson, A Walfisch, S Delgado, B Shechter-Maor, G Delgado, J Fich, A Gheber, L |
author_facet | Mermelshtein, A Gerson, A Walfisch, S Delgado, B Shechter-Maor, G Delgado, J Fich, A Gheber, L |
author_sort | Mermelshtein, A |
collection | PubMed |
description | Cyclins D1, D2 and D3 play important roles in cell proliferation and differentiation. Although their abnormal expression has been linked to cancer development and progression in a number of tissues, the expression of cyclin D2 and D3 proteins in colon cancer has not yet been characterised. In this study, we examined cyclin D1, D2 and D3 protein expression by Western blot analysis in tumour and adjacent normal colon tissues of 57 patients. In addition, we examined D-type cyclins protein expression in HT29 and LoVo39 cell lines from colon carcinomas, as a function of induced proliferation and differentiation. In both cell lines, the expression of the three D-type cyclins increased as a result of induced proliferation, whereas the expression of cyclin D3 increased as a result of induced differentiation. In colon tumours, cyclin D1 was overexpressed in 44%, cyclin D2 was overexpressed in 53% and cyclin D3 was overexpressed in 35% of the cases. We also found that in 16% of the cases, cyclin D3 protein expression was reduced in the tumour, as compared to the adjacent normal tissue. Examination of D-type cyclin protein overexpression in relation to the TNM stage of the tumours revealed that overexpression of cyclins D1 and/or D2, but not cyclin D3, is linked to colon carcinogenesis and that overexpression of cyclin D2 may be related to a higher TNM stage of the tumour. |
format | Text |
id | pubmed-2361572 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23615722009-09-10 Expression of D-type cyclins in colon cancer and in cell lines from colon carcinomas Mermelshtein, A Gerson, A Walfisch, S Delgado, B Shechter-Maor, G Delgado, J Fich, A Gheber, L Br J Cancer Molecular Diagnostics Cyclins D1, D2 and D3 play important roles in cell proliferation and differentiation. Although their abnormal expression has been linked to cancer development and progression in a number of tissues, the expression of cyclin D2 and D3 proteins in colon cancer has not yet been characterised. In this study, we examined cyclin D1, D2 and D3 protein expression by Western blot analysis in tumour and adjacent normal colon tissues of 57 patients. In addition, we examined D-type cyclins protein expression in HT29 and LoVo39 cell lines from colon carcinomas, as a function of induced proliferation and differentiation. In both cell lines, the expression of the three D-type cyclins increased as a result of induced proliferation, whereas the expression of cyclin D3 increased as a result of induced differentiation. In colon tumours, cyclin D1 was overexpressed in 44%, cyclin D2 was overexpressed in 53% and cyclin D3 was overexpressed in 35% of the cases. We also found that in 16% of the cases, cyclin D3 protein expression was reduced in the tumour, as compared to the adjacent normal tissue. Examination of D-type cyclin protein overexpression in relation to the TNM stage of the tumours revealed that overexpression of cyclins D1 and/or D2, but not cyclin D3, is linked to colon carcinogenesis and that overexpression of cyclin D2 may be related to a higher TNM stage of the tumour. Nature Publishing Group 2005-08-08 2005-07-12 /pmc/articles/PMC2361572/ /pubmed/16012517 http://dx.doi.org/10.1038/sj.bjc.6602709 Text en Copyright © 2005 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 Mermelshtein, A Gerson, A Walfisch, S Delgado, B Shechter-Maor, G Delgado, J Fich, A Gheber, L Expression of D-type cyclins in colon cancer and in cell lines from colon carcinomas |
title | Expression of D-type cyclins in colon cancer and in cell lines from colon carcinomas |
title_full | Expression of D-type cyclins in colon cancer and in cell lines from colon carcinomas |
title_fullStr | Expression of D-type cyclins in colon cancer and in cell lines from colon carcinomas |
title_full_unstemmed | Expression of D-type cyclins in colon cancer and in cell lines from colon carcinomas |
title_short | Expression of D-type cyclins in colon cancer and in cell lines from colon carcinomas |
title_sort | expression of d-type cyclins in colon cancer and in cell lines from colon carcinomas |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361572/ https://www.ncbi.nlm.nih.gov/pubmed/16012517 http://dx.doi.org/10.1038/sj.bjc.6602709 |
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