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p53 codon 72 polymorphism and coronary artery disease: Evidence of interaction with ACP(1)

BACKGROUND: Common biological features between cancer and atherosclerosis suggest possible association of p53 with atherosclerotic diseases, but data on such a relationship are controversial, suggesting interactions with other variables. Acid phosphatase locus 1 (ACP(1)) is a polymorphic gene that c...

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Autores principales: Gloria-Bottini, Fulvia, Banci, Maria, Saccucci, Patrizia, Neri, Anna, Bottini, Egidio, Magrini, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3560788/
https://www.ncbi.nlm.nih.gov/pubmed/23197232
http://dx.doi.org/10.12659/MSM.883597
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author Gloria-Bottini, Fulvia
Banci, Maria
Saccucci, Patrizia
Neri, Anna
Bottini, Egidio
Magrini, Andrea
author_facet Gloria-Bottini, Fulvia
Banci, Maria
Saccucci, Patrizia
Neri, Anna
Bottini, Egidio
Magrini, Andrea
author_sort Gloria-Bottini, Fulvia
collection PubMed
description BACKGROUND: Common biological features between cancer and atherosclerosis suggest possible association of p53 with atherosclerotic diseases, but data on such a relationship are controversial, suggesting interactions with other variables. Acid phosphatase locus 1 (ACP(1)) is a polymorphic gene that controls the synthesis of an enzyme involved in important metabolic functions. Since ACP(1) is associated with coronary artery disease (CAD), we searched for possible interactions between this enzyme and p53 codon 72 polymorphism with regard to their effects on susceptibility to CAD. MATERIAL/METHODS: The study included 381 patients admitted to the hospital for cardiovascular disease (232 patients with CAD and 149 with other cardiovascular problems) and 97 healthy newborns. RESULTS: The proportion of subjects carrying the *Pro allele of p53 codon 72 and the high activity *B*C genotype of ACP(1) is higher in CAD (10.3%) than in non-CAD patients (2.0%) and in healthy newborns (6.2%). CONCLUSIONS: The data suggest an interaction between p53 codon 72 and ACP(1) wherein a positive effect of the p53 *Pro allele on susceptibility to CAD occurs, but only in the presence of the ACP(1) genotype characterized by high enzymatic activity.
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spelling pubmed-35607882013-04-24 p53 codon 72 polymorphism and coronary artery disease: Evidence of interaction with ACP(1) Gloria-Bottini, Fulvia Banci, Maria Saccucci, Patrizia Neri, Anna Bottini, Egidio Magrini, Andrea Med Sci Monit Clinical Research BACKGROUND: Common biological features between cancer and atherosclerosis suggest possible association of p53 with atherosclerotic diseases, but data on such a relationship are controversial, suggesting interactions with other variables. Acid phosphatase locus 1 (ACP(1)) is a polymorphic gene that controls the synthesis of an enzyme involved in important metabolic functions. Since ACP(1) is associated with coronary artery disease (CAD), we searched for possible interactions between this enzyme and p53 codon 72 polymorphism with regard to their effects on susceptibility to CAD. MATERIAL/METHODS: The study included 381 patients admitted to the hospital for cardiovascular disease (232 patients with CAD and 149 with other cardiovascular problems) and 97 healthy newborns. RESULTS: The proportion of subjects carrying the *Pro allele of p53 codon 72 and the high activity *B*C genotype of ACP(1) is higher in CAD (10.3%) than in non-CAD patients (2.0%) and in healthy newborns (6.2%). CONCLUSIONS: The data suggest an interaction between p53 codon 72 and ACP(1) wherein a positive effect of the p53 *Pro allele on susceptibility to CAD occurs, but only in the presence of the ACP(1) genotype characterized by high enzymatic activity. International Scientific Literature, Inc. 2012-12-01 /pmc/articles/PMC3560788/ /pubmed/23197232 http://dx.doi.org/10.12659/MSM.883597 Text en © Med Sci Monit, 2011 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License.
spellingShingle Clinical Research
Gloria-Bottini, Fulvia
Banci, Maria
Saccucci, Patrizia
Neri, Anna
Bottini, Egidio
Magrini, Andrea
p53 codon 72 polymorphism and coronary artery disease: Evidence of interaction with ACP(1)
title p53 codon 72 polymorphism and coronary artery disease: Evidence of interaction with ACP(1)
title_full p53 codon 72 polymorphism and coronary artery disease: Evidence of interaction with ACP(1)
title_fullStr p53 codon 72 polymorphism and coronary artery disease: Evidence of interaction with ACP(1)
title_full_unstemmed p53 codon 72 polymorphism and coronary artery disease: Evidence of interaction with ACP(1)
title_short p53 codon 72 polymorphism and coronary artery disease: Evidence of interaction with ACP(1)
title_sort p53 codon 72 polymorphism and coronary artery disease: evidence of interaction with acp(1)
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3560788/
https://www.ncbi.nlm.nih.gov/pubmed/23197232
http://dx.doi.org/10.12659/MSM.883597
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