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Relationship between codon 249 mutation in exon 7 of p53 gene and diagnosis of hepatocellular carcinoma

INTRODUCTION: Hepatocellular carcinoma (HCC) is one of the most common malignancies worldwide. Multiple genetic and epigenetic changes are involved in the molecular pathogenesis of HCC. Heat shock proteins have essential roles in protecting cells from the potentially lethal effects of stress. Among...

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Autores principales: El-Din, Hesham Gamal, Ghafar, Nagwa Abdel, Saad, Nevine E., Aziz, Mona, Rasheed, Dina, Hassan, Eman Mahmoud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3282511/
https://www.ncbi.nlm.nih.gov/pubmed/22371770
http://dx.doi.org/10.5114/aoms.2010.14254
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author El-Din, Hesham Gamal
Ghafar, Nagwa Abdel
Saad, Nevine E.
Aziz, Mona
Rasheed, Dina
Hassan, Eman Mahmoud
author_facet El-Din, Hesham Gamal
Ghafar, Nagwa Abdel
Saad, Nevine E.
Aziz, Mona
Rasheed, Dina
Hassan, Eman Mahmoud
author_sort El-Din, Hesham Gamal
collection PubMed
description INTRODUCTION: Hepatocellular carcinoma (HCC) is one of the most common malignancies worldwide. Multiple genetic and epigenetic changes are involved in the molecular pathogenesis of HCC. Heat shock proteins have essential roles in protecting cells from the potentially lethal effects of stress. Among them, HSP70 are often overexpressed in cells of various cancers and have been suggested to contribute to tumourigenesis. p53 mutations in codon 249 have also been identified in HCC. MATERIAL AND METHODS: Fifty patients with liver disease were enrolled in this study compared to 10 healthy volunteers. The studied patients were divided into 2 groups: group I includes those suffering from HCC, group II includes those suffering from post-hepatitis B and C liver cirrhosis. The presence of p53 gene mutation was detected by DNA extraction from whole blood of patients and controls followed by polymerase chain reaction then restriction fragment length polymorphism (RFLP) analysis of codon 249 of exon 7. We also studied the genotypes of the HSP70 gene by PCR followed by RFLP analysis. RESULTS: Our results revealed no statistical difference between group I, group II, and the control group as regards exon 7 mutation of the p53 gene. Also the frequency of polymorphic genotypes of HSP70 showed no significant difference between the 3 studied groups. CONCLUSIONS: The present study supports the view that the incidence of point mutation of p53 codon 249 mutations in exon 7 of the p53 gene may not play a role in carcinogenesis of HCC in Egyptian patients. Also, genetic polymorphism in HSP70 was not associated with high risk of future development of HCC.
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spelling pubmed-32825112012-02-27 Relationship between codon 249 mutation in exon 7 of p53 gene and diagnosis of hepatocellular carcinoma El-Din, Hesham Gamal Ghafar, Nagwa Abdel Saad, Nevine E. Aziz, Mona Rasheed, Dina Hassan, Eman Mahmoud Arch Med Sci Clinical Research INTRODUCTION: Hepatocellular carcinoma (HCC) is one of the most common malignancies worldwide. Multiple genetic and epigenetic changes are involved in the molecular pathogenesis of HCC. Heat shock proteins have essential roles in protecting cells from the potentially lethal effects of stress. Among them, HSP70 are often overexpressed in cells of various cancers and have been suggested to contribute to tumourigenesis. p53 mutations in codon 249 have also been identified in HCC. MATERIAL AND METHODS: Fifty patients with liver disease were enrolled in this study compared to 10 healthy volunteers. The studied patients were divided into 2 groups: group I includes those suffering from HCC, group II includes those suffering from post-hepatitis B and C liver cirrhosis. The presence of p53 gene mutation was detected by DNA extraction from whole blood of patients and controls followed by polymerase chain reaction then restriction fragment length polymorphism (RFLP) analysis of codon 249 of exon 7. We also studied the genotypes of the HSP70 gene by PCR followed by RFLP analysis. RESULTS: Our results revealed no statistical difference between group I, group II, and the control group as regards exon 7 mutation of the p53 gene. Also the frequency of polymorphic genotypes of HSP70 showed no significant difference between the 3 studied groups. CONCLUSIONS: The present study supports the view that the incidence of point mutation of p53 codon 249 mutations in exon 7 of the p53 gene may not play a role in carcinogenesis of HCC in Egyptian patients. Also, genetic polymorphism in HSP70 was not associated with high risk of future development of HCC. Termedia Publishing House 2010-06-30 2010-06-30 /pmc/articles/PMC3282511/ /pubmed/22371770 http://dx.doi.org/10.5114/aoms.2010.14254 Text en Copyright © 2010 Termedia & Banach http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Research
El-Din, Hesham Gamal
Ghafar, Nagwa Abdel
Saad, Nevine E.
Aziz, Mona
Rasheed, Dina
Hassan, Eman Mahmoud
Relationship between codon 249 mutation in exon 7 of p53 gene and diagnosis of hepatocellular carcinoma
title Relationship between codon 249 mutation in exon 7 of p53 gene and diagnosis of hepatocellular carcinoma
title_full Relationship between codon 249 mutation in exon 7 of p53 gene and diagnosis of hepatocellular carcinoma
title_fullStr Relationship between codon 249 mutation in exon 7 of p53 gene and diagnosis of hepatocellular carcinoma
title_full_unstemmed Relationship between codon 249 mutation in exon 7 of p53 gene and diagnosis of hepatocellular carcinoma
title_short Relationship between codon 249 mutation in exon 7 of p53 gene and diagnosis of hepatocellular carcinoma
title_sort relationship between codon 249 mutation in exon 7 of p53 gene and diagnosis of hepatocellular carcinoma
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3282511/
https://www.ncbi.nlm.nih.gov/pubmed/22371770
http://dx.doi.org/10.5114/aoms.2010.14254
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