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The significance of p53 codon 72 polymorphism for the development of cervical adenocarcinomas
Infection with the human papillomavirus is an important co-factor in the development of cervical carcinomas. Accordingly, HPV DNA is recognised in most of these tumours. Polymorphism of the p53 gene, codon 72, is also considered a risk factor in the development of cervical carcinoma. However, this f...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2001
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375157/ https://www.ncbi.nlm.nih.gov/pubmed/11710828 http://dx.doi.org/10.1054/bjoc.2001.2085 |
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author | Andersson, S Rylander, E Strand, A Sällström, J Wilander, E |
author_facet | Andersson, S Rylander, E Strand, A Sällström, J Wilander, E |
author_sort | Andersson, S |
collection | PubMed |
description | Infection with the human papillomavirus is an important co-factor in the development of cervical carcinomas. Accordingly, HPV DNA is recognised in most of these tumours. Polymorphism of the p53 gene, codon 72, is also considered a risk factor in the development of cervical carcinoma. However, this finding is contradicted by several observers. In the present investigation, 111 cases of adenocarcinoma of the cervix collected through the Swedish Cancer Registry and 188 controls (females with normal cytology at organised gynaecological screening) were analysed with regard to p53, codon 72, polymorphism using a PCR- and SSCP-based technique. In the controls, 9% showed pro/pro, 44% pro/arg and 47% arg/arg, whereas in the invasive adenocarcinomas, the corresponding figures were 0%, 29% and 71%, respectively. The difference was statistically significant (P = 0.001). HPV DNA was identified in 86 tumours (HPV 18 in 48, HPV 16 in 31 and HPV of unknown type in 7 cases) and 25 tumours were HPV negative. The p53, codon 72, genotypes observed in HPV-positive and HPV-negative cervical adenocarcinomas were not statistically different (P = 0.690). The results indicate that women homozygotic for arg/arg in codon 72 of the p53 gene are at an increased risk for the development of cervical adenocarcinomas. However, this genetic disposition seems to be unrelated to the HPV infection. © 2001 Cancer Research Campaign http://www.bjcancer.com |
format | Text |
id | pubmed-2375157 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2001 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23751572009-09-10 The significance of p53 codon 72 polymorphism for the development of cervical adenocarcinomas Andersson, S Rylander, E Strand, A Sällström, J Wilander, E Br J Cancer Regular Article Infection with the human papillomavirus is an important co-factor in the development of cervical carcinomas. Accordingly, HPV DNA is recognised in most of these tumours. Polymorphism of the p53 gene, codon 72, is also considered a risk factor in the development of cervical carcinoma. However, this finding is contradicted by several observers. In the present investigation, 111 cases of adenocarcinoma of the cervix collected through the Swedish Cancer Registry and 188 controls (females with normal cytology at organised gynaecological screening) were analysed with regard to p53, codon 72, polymorphism using a PCR- and SSCP-based technique. In the controls, 9% showed pro/pro, 44% pro/arg and 47% arg/arg, whereas in the invasive adenocarcinomas, the corresponding figures were 0%, 29% and 71%, respectively. The difference was statistically significant (P = 0.001). HPV DNA was identified in 86 tumours (HPV 18 in 48, HPV 16 in 31 and HPV of unknown type in 7 cases) and 25 tumours were HPV negative. The p53, codon 72, genotypes observed in HPV-positive and HPV-negative cervical adenocarcinomas were not statistically different (P = 0.690). The results indicate that women homozygotic for arg/arg in codon 72 of the p53 gene are at an increased risk for the development of cervical adenocarcinomas. However, this genetic disposition seems to be unrelated to the HPV infection. © 2001 Cancer Research Campaign http://www.bjcancer.com Nature Publishing Group 2001-10 /pmc/articles/PMC2375157/ /pubmed/11710828 http://dx.doi.org/10.1054/bjoc.2001.2085 Text en Copyright © 2001 Cancer Research Campaign 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 | Regular Article Andersson, S Rylander, E Strand, A Sällström, J Wilander, E The significance of p53 codon 72 polymorphism for the development of cervical adenocarcinomas |
title | The significance of p53 codon 72 polymorphism for the development of cervical adenocarcinomas |
title_full | The significance of p53 codon 72 polymorphism for the development of cervical adenocarcinomas |
title_fullStr | The significance of p53 codon 72 polymorphism for the development of cervical adenocarcinomas |
title_full_unstemmed | The significance of p53 codon 72 polymorphism for the development of cervical adenocarcinomas |
title_short | The significance of p53 codon 72 polymorphism for the development of cervical adenocarcinomas |
title_sort | significance of p53 codon 72 polymorphism for the development of cervical adenocarcinomas |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375157/ https://www.ncbi.nlm.nih.gov/pubmed/11710828 http://dx.doi.org/10.1054/bjoc.2001.2085 |
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