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Protein kinase A (PK-A) regulatory subunit expression in colorectal cancer and related mucosa.
Photoaffinity labelling (PAL) with [32P]8-azido-cAMP and polyacrylamide gel electrophoresis (PAGE) has been used to identify three specific cAMP-binding proteins (cAMP-BPs) within cytosols derived from the centre and periphery of 32 human colorectal cancers and from related adjacent (less than 5 cm...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1994
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1968829/ https://www.ncbi.nlm.nih.gov/pubmed/8142263 |
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author | Bradbury, A. W. Carter, D. C. Miller, W. R. Cho-Chung, Y. S. Clair, T. |
author_facet | Bradbury, A. W. Carter, D. C. Miller, W. R. Cho-Chung, Y. S. Clair, T. |
author_sort | Bradbury, A. W. |
collection | PubMed |
description | Photoaffinity labelling (PAL) with [32P]8-azido-cAMP and polyacrylamide gel electrophoresis (PAGE) has been used to identify three specific cAMP-binding proteins (cAMP-BPs) within cytosols derived from the centre and periphery of 32 human colorectal cancers and from related adjacent (less than 5 cm from the tumour) and distant (more than 5 cm from the tumour) microscopically benign mucosa. By immunoprecipitation with specific anti-RI and anti-RII antibodies these proteins have subsequently been characterised as a single form of RI (48 kDa) and two forms of RII (50 and 52 kDa). The relative expression of isoforms in each specimen has been quantified by laser densitometry. There was significantly more RI expressed in both tumour centre and periphery than in either adjacent or distant mucosa (P < 0.008 by Wilcoxon signed-rank test). There was no significant difference in relative RI expression between tumour centre and periphery, or between adjacent and distant mucosa. There was no association between relative RI expression and Dukes' stage. Poorly differentiated tumours expressed significantly more RI than those that were either moderately or well differentiated (P = 0.016 by Mann-Whitney U-test). This study is the first to have characterised cAMP-BPs within human colorectal tissues and has demonstrated that colorectal cancers, and in particular those of poor histological grade, relatively overexpress RI when compared with related benign mucosa. IMAGES: |
format | Text |
id | pubmed-1968829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1994 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-19688292009-09-10 Protein kinase A (PK-A) regulatory subunit expression in colorectal cancer and related mucosa. Bradbury, A. W. Carter, D. C. Miller, W. R. Cho-Chung, Y. S. Clair, T. Br J Cancer Research Article Photoaffinity labelling (PAL) with [32P]8-azido-cAMP and polyacrylamide gel electrophoresis (PAGE) has been used to identify three specific cAMP-binding proteins (cAMP-BPs) within cytosols derived from the centre and periphery of 32 human colorectal cancers and from related adjacent (less than 5 cm from the tumour) and distant (more than 5 cm from the tumour) microscopically benign mucosa. By immunoprecipitation with specific anti-RI and anti-RII antibodies these proteins have subsequently been characterised as a single form of RI (48 kDa) and two forms of RII (50 and 52 kDa). The relative expression of isoforms in each specimen has been quantified by laser densitometry. There was significantly more RI expressed in both tumour centre and periphery than in either adjacent or distant mucosa (P < 0.008 by Wilcoxon signed-rank test). There was no significant difference in relative RI expression between tumour centre and periphery, or between adjacent and distant mucosa. There was no association between relative RI expression and Dukes' stage. Poorly differentiated tumours expressed significantly more RI than those that were either moderately or well differentiated (P = 0.016 by Mann-Whitney U-test). This study is the first to have characterised cAMP-BPs within human colorectal tissues and has demonstrated that colorectal cancers, and in particular those of poor histological grade, relatively overexpress RI when compared with related benign mucosa. IMAGES: Nature Publishing Group 1994-04 /pmc/articles/PMC1968829/ /pubmed/8142263 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 Bradbury, A. W. Carter, D. C. Miller, W. R. Cho-Chung, Y. S. Clair, T. Protein kinase A (PK-A) regulatory subunit expression in colorectal cancer and related mucosa. |
title | Protein kinase A (PK-A) regulatory subunit expression in colorectal cancer and related mucosa. |
title_full | Protein kinase A (PK-A) regulatory subunit expression in colorectal cancer and related mucosa. |
title_fullStr | Protein kinase A (PK-A) regulatory subunit expression in colorectal cancer and related mucosa. |
title_full_unstemmed | Protein kinase A (PK-A) regulatory subunit expression in colorectal cancer and related mucosa. |
title_short | Protein kinase A (PK-A) regulatory subunit expression in colorectal cancer and related mucosa. |
title_sort | protein kinase a (pk-a) regulatory subunit expression in colorectal cancer and related mucosa. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1968829/ https://www.ncbi.nlm.nih.gov/pubmed/8142263 |
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