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Coexpression of cdk2/cdc2 and retinoblastoma gene products in colorectal cancer.
The retinoblastoma gene (Rb gene) is a tumour-suppressor gene and its product (pRB) is known to act as a negative regulator of the cell cycle. Although lack of pRB expression resulting from gene alterations is considered to be responsible for the genesis of several human malignancies, increased expr...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1995
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033831/ https://www.ncbi.nlm.nih.gov/pubmed/7779716 |
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author | Yamamoto, H. Monden, T. Ikeda, K. Izawa, H. Fukuda, K. Fukunaga, M. Tomita, N. Shimano, T. Shiozaki, H. Monden, M. |
author_facet | Yamamoto, H. Monden, T. Ikeda, K. Izawa, H. Fukuda, K. Fukunaga, M. Tomita, N. Shimano, T. Shiozaki, H. Monden, M. |
author_sort | Yamamoto, H. |
collection | PubMed |
description | The retinoblastoma gene (Rb gene) is a tumour-suppressor gene and its product (pRB) is known to act as a negative regulator of the cell cycle. Although lack of pRB expression resulting from gene alterations is considered to be responsible for the genesis of several human malignancies, increased expression of pRB has been demonstrated in a majority of colorectal cancer cases. In the present study, we investigated the expression of pRB as well as that of its related kinases, cdk2 and cdc2, in colorectal cancer, since these kinases have been reported to phosphorylate and inactivate pRB. Western blot analysis revealed that colorectal cancer expressed higher levels of cdk2 and cdc2 than did normal mucosa and that the ratio of the hyperphosphorylated form of pRB was higher in colorectal cancer. Furthermore, immunohistochemical studies showed that cdk2/cdc2 was expressed exclusively in the cancer cells positive for pRB. These results suggest that an increase in the expression of cdk2/cdc2 in colorectal cancer may have prevented pRB from braking the cell cycle through phosphorylation. IMAGES: |
format | Text |
id | pubmed-2033831 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1995 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20338312009-09-10 Coexpression of cdk2/cdc2 and retinoblastoma gene products in colorectal cancer. Yamamoto, H. Monden, T. Ikeda, K. Izawa, H. Fukuda, K. Fukunaga, M. Tomita, N. Shimano, T. Shiozaki, H. Monden, M. Br J Cancer Research Article The retinoblastoma gene (Rb gene) is a tumour-suppressor gene and its product (pRB) is known to act as a negative regulator of the cell cycle. Although lack of pRB expression resulting from gene alterations is considered to be responsible for the genesis of several human malignancies, increased expression of pRB has been demonstrated in a majority of colorectal cancer cases. In the present study, we investigated the expression of pRB as well as that of its related kinases, cdk2 and cdc2, in colorectal cancer, since these kinases have been reported to phosphorylate and inactivate pRB. Western blot analysis revealed that colorectal cancer expressed higher levels of cdk2 and cdc2 than did normal mucosa and that the ratio of the hyperphosphorylated form of pRB was higher in colorectal cancer. Furthermore, immunohistochemical studies showed that cdk2/cdc2 was expressed exclusively in the cancer cells positive for pRB. These results suggest that an increase in the expression of cdk2/cdc2 in colorectal cancer may have prevented pRB from braking the cell cycle through phosphorylation. IMAGES: Nature Publishing Group 1995-06 /pmc/articles/PMC2033831/ /pubmed/7779716 Text en 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 | Research Article Yamamoto, H. Monden, T. Ikeda, K. Izawa, H. Fukuda, K. Fukunaga, M. Tomita, N. Shimano, T. Shiozaki, H. Monden, M. Coexpression of cdk2/cdc2 and retinoblastoma gene products in colorectal cancer. |
title | Coexpression of cdk2/cdc2 and retinoblastoma gene products in colorectal cancer. |
title_full | Coexpression of cdk2/cdc2 and retinoblastoma gene products in colorectal cancer. |
title_fullStr | Coexpression of cdk2/cdc2 and retinoblastoma gene products in colorectal cancer. |
title_full_unstemmed | Coexpression of cdk2/cdc2 and retinoblastoma gene products in colorectal cancer. |
title_short | Coexpression of cdk2/cdc2 and retinoblastoma gene products in colorectal cancer. |
title_sort | coexpression of cdk2/cdc2 and retinoblastoma gene products in colorectal cancer. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033831/ https://www.ncbi.nlm.nih.gov/pubmed/7779716 |
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