Sp. Irazusta et al., THE VALUE OF PCNA AND AGNOR STAINING IN ENDOSCOPIC BIOPSIES OF GASTRIC-MUCOSA, Pathology research and practice, 194(1), 1998, pp. 33-39
The aim of the present study was to examine the usefulness of the quan
tification of PC10-positive-cells and of Argyrophilic Nucleolar Organi
zer Regions (AgNORs) in gastric biopsies for the identification of gas
tric mucosal proliferative lesions. Fifty seven paraffin-embedded endo
scopic biopsies were classified into four histologic groups: normal, i
nflammatory, dysplastic and neoplastic mucosa. The percentage of PC10-
positive cells was determined by immunohistochemistry. The AgNOR param
eters determined included the total number of all identifiable silver
precipitations in the nucleus, the mean number of silver precipitation
s per cluster, and the presence of morphologically heterogenous silver
precipitations. Group comparisons were performed using the Kruskall W
allis and Dunn non-parametric tests with a significance level of 5%. A
dicriminant analysis (followed by the jack-knife procedure) was perfo
rmed using the three AgNOR parameters plus the percentage of PCNA-posi
tive cells as the independent variables and histological groups as the
dependent variable. All three AgNOR parameters, as well as the percen
tage of PCNA-stained nuclei, showed their highest values in the carcin
oma group. However, no good differentiation among the four histologic
groups was obtained using only one of these parameters, since there wa
s always considerable overlap among them. By combining all the paramet
ers in a linear discriminant analysis, we obtained a correct classific
ation in 48 out of 57 cases. Within the classification errors there wa
s only one false positive carcinoma, which was in fact a dysplasia and
only one false negative carcinoma erroneously classified as dysplasia
. The number of cells with heterogenous AgNORs was the most important
parameter for the discriminant analysis. No correlation between PCNA v
alues and the AgNOR parameters could be found, thus indicating that th
ey do not represent the same phenomenon in the cell cycle. We conclude
d that the use of a combination of various proliferation parameters in
a linear discriminant analysis may be helpful for differentiating gas
tric mucosal lesions. The peculiar AgNOR morphology is an important va
riable which should be taken in consideration in quantitative studies.
PCNA and AgNORs seem to represent different physiological phenomena i
n the cell cycle.