p53 codon 72 polymorphism and coronary artery disease: evidence of interaction with ACP₁

Med Sci Monit. 2012 Dec;18(12):CR712-5. doi: 10.12659/msm.883597.

Abstract

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 (ACPACP₁) is a polymorphic gene that controls the synthesis of an enzyme involved in important metabolic functions. Since ACPACP₁ 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 ACPACP₁ 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 ACPACP₁ wherein a positive effect of the p53 *Pro allele on susceptibility to CAD occurs, but only in the presence of the ACPACP₁ genotype characterized by high enzymatic activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Alleles
  • Codon / genetics*
  • Coronary Artery Disease / genetics*
  • Female
  • Genetic Predisposition to Disease*
  • Hospitalization
  • Humans
  • Infant, Newborn
  • Male
  • Polymorphism, Single Nucleotide / genetics*
  • Protein Tyrosine Phosphatases / metabolism*
  • Proto-Oncogene Proteins / metabolism*
  • Tumor Suppressor Protein p53 / genetics*

Substances

  • Codon
  • Proto-Oncogene Proteins
  • Tumor Suppressor Protein p53
  • ACP1 protein, human
  • Protein Tyrosine Phosphatases