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Overexpression of p53 mRNA in colorectal cancer and its relationship to p53 gene mutation.

We analysed the frequency of p53 mRNA overexpression in a series of 109 primary colorectal carcinomas and its association with p53 gene mutation, which has been correlated with short survival. Sixty-nine of the 109 cases (63%) demonstrated p53 mRNA overexpression, without any correlation with stage...

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Autores principales: el-Mahdani, N., Vaillant, J. C., Guiguet, M., Prévot, S., Bertrand, V., Bernard, C., Parc, R., Béréziat, G., Hermelin, B.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group|1 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2063311/
https://www.ncbi.nlm.nih.gov/pubmed/9052405
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author el-Mahdani, N.
Vaillant, J. C.
Guiguet, M.
Prévot, S.
Bertrand, V.
Bernard, C.
Parc, R.
Béréziat, G.
Hermelin, B.
author_facet el-Mahdani, N.
Vaillant, J. C.
Guiguet, M.
Prévot, S.
Bertrand, V.
Bernard, C.
Parc, R.
Béréziat, G.
Hermelin, B.
author_sort el-Mahdani, N.
collection PubMed
description We analysed the frequency of p53 mRNA overexpression in a series of 109 primary colorectal carcinomas and its association with p53 gene mutation, which has been correlated with short survival. Sixty-nine of the 109 cases (63%) demonstrated p53 mRNA overexpression, without any correlation with stage or site of disease. Comparison with p53 gene mutation indicated that, besides cases in which p53 gene mutation and p53 mRNA overexpression were either both present (40 cases) or both absent (36 cases), there were also cases in which p53 mRNA was overexpressed in the absence of any mutation (29 cases) and those with a mutant gene in which the mRNA was not overexpressed (four cases). Moreover, the mutant p53 tumours exhibited an increase of p53 mRNA expression, which was significantly higher in tumours expressing the mutated allele alone than in tumours expressing both wild- and mutated-type alleles. These data (1) show that p53 mRNA overexpression is a frequent event in colorectal tumours and is not predictive of the status of the gene, i.e. whether or not a mutation is present; (2) provide further evidence that p53 protein overexpression does not only result from an increase in the half-life of mutated p53 and suggest that inactivation of the p53 function in colorectal cancers involves at least two distinct mechanisms, including p53 overexpression and/or mutation; and (3) suggest that p53 mRNA overexpression is an early event, since it is not correlated with Dukes stage.
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spelling pubmed-20633112009-09-10 Overexpression of p53 mRNA in colorectal cancer and its relationship to p53 gene mutation. el-Mahdani, N. Vaillant, J. C. Guiguet, M. Prévot, S. Bertrand, V. Bernard, C. Parc, R. Béréziat, G. Hermelin, B. Br J Cancer Research Article We analysed the frequency of p53 mRNA overexpression in a series of 109 primary colorectal carcinomas and its association with p53 gene mutation, which has been correlated with short survival. Sixty-nine of the 109 cases (63%) demonstrated p53 mRNA overexpression, without any correlation with stage or site of disease. Comparison with p53 gene mutation indicated that, besides cases in which p53 gene mutation and p53 mRNA overexpression were either both present (40 cases) or both absent (36 cases), there were also cases in which p53 mRNA was overexpressed in the absence of any mutation (29 cases) and those with a mutant gene in which the mRNA was not overexpressed (four cases). Moreover, the mutant p53 tumours exhibited an increase of p53 mRNA expression, which was significantly higher in tumours expressing the mutated allele alone than in tumours expressing both wild- and mutated-type alleles. These data (1) show that p53 mRNA overexpression is a frequent event in colorectal tumours and is not predictive of the status of the gene, i.e. whether or not a mutation is present; (2) provide further evidence that p53 protein overexpression does not only result from an increase in the half-life of mutated p53 and suggest that inactivation of the p53 function in colorectal cancers involves at least two distinct mechanisms, including p53 overexpression and/or mutation; and (3) suggest that p53 mRNA overexpression is an early event, since it is not correlated with Dukes stage. Nature Publishing Group|1 1997 /pmc/articles/PMC2063311/ /pubmed/9052405 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
el-Mahdani, N.
Vaillant, J. C.
Guiguet, M.
Prévot, S.
Bertrand, V.
Bernard, C.
Parc, R.
Béréziat, G.
Hermelin, B.
Overexpression of p53 mRNA in colorectal cancer and its relationship to p53 gene mutation.
title Overexpression of p53 mRNA in colorectal cancer and its relationship to p53 gene mutation.
title_full Overexpression of p53 mRNA in colorectal cancer and its relationship to p53 gene mutation.
title_fullStr Overexpression of p53 mRNA in colorectal cancer and its relationship to p53 gene mutation.
title_full_unstemmed Overexpression of p53 mRNA in colorectal cancer and its relationship to p53 gene mutation.
title_short Overexpression of p53 mRNA in colorectal cancer and its relationship to p53 gene mutation.
title_sort overexpression of p53 mrna in colorectal cancer and its relationship to p53 gene mutation.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2063311/
https://www.ncbi.nlm.nih.gov/pubmed/9052405
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