Abstract
BACKGROUND
Currently, there is a surge of interest on the possible relationship between cancer and acid phosphatase locus 1 (ACP(1)),
an enzyme involved in the modulation of growth factors and cellular metabolism. As far as the authors know, the possible relationship
between ACP(1) genetic variability and cancer grading has not yet been considered. In this article, the authors have studied
the relationship between ACP(1) genotype and grade in colon and endometrium cancers.
METHODS
Seventy-one patients with colon cancer and 71 patients with endometrium cancer were studied. ACP(1) genotype was determined
by DNA analysis. Three-way contingency table analysis was carried out according to Sokal and Rohlf. Other statistical analyses
were performed using SPSS programs.
RESULTS
There is a significant association between ACP(1) and cancer grade mainly due to ACP(1) genotypes carrying the *C allele that
are much less represented in patients with low grade when compared with those with high grade. In both cancers, the concentration
of S isoform is significantly lower in low grade than in high grade. The relationship between ACP(1) and grade is the same
in the 2 cancers.
CONCLUSIONS
Assuming the presence of diverse classes of cancer, the role of ACP(1) in the modulation of growth factors and cellular metabolism
could have significant effects in less aggressive forms but not in more aggressive ones.
Links
Authors
Gloria-Bottini F, Spina C, Nicotra M, Saccucci P, Ambrosi S, Bottini E
Institution
Division of Human Populations Biopathology and Environmental Pathology, Department of Biopathology and Imaging Diagnostics, School of Medicine, University of Rome Tor Vergata, Rome, Italy. gloria@med.uniroma2.it
Source
The American journal of the medical sciences 344:1 2012 Jul pg 32-4MeSH
AgedColonic Neoplasms
Endometrial Neoplasms
Female
Genetic Predisposition to Disease
Humans
Male
Middle Aged
Neoplasm Grading
Odds Ratio
Polymorphism, Genetic
Protein Isoforms
Protein Tyrosine Phosphatases
Proto-Oncogene Proteins
Rome
Pub Type(s)
Journal ArticleLanguage
eng
PubMed ID
22692348
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