Immunohistochemical study of pS2 protein in gastric
carcinoma and normal gastric mucosa
Kominea A., Kapranos N., Vandoros G., Kokka E., Sotiropoulou
G.
Departments of Pathology Aegion General Hospital, and Amalia
Fleming Hospital, Melissia, Athens, Laboratory of Anatomy, Medical
School, University of Patras
The aim of the present study was to examine the expression of
pS2 protein in gastric carcinomas and normal gastric mucosa. Ninety
cases of gastric carcinoma surgically removed by total or partial
gastrectomy from 48 males and 42 females, 37-86 years old, were
included in this study. Detection of pS2 protein was performed immunohistochemically by the use of monoclonal antibody and
the staining was scored by an Histoscore system from 0 to 12 grades.
Cytoplasmic immunostaining was detected in 55 cases (61%) of
gastric carcinoma and in all examined cases of normal gastric
mucosa near the tumors. In normal gastric mucosa the immunoreaction
was localized in subnuclear and perinuclear region of the superficial epithelium and the upper two thirds of the foveolae, as well
as in luminal secretions, whereas the deeper glands were negative.
In the regions of epithelial dysplasia or intestinal metaplasia
which were coexistent with the tumors, the staining was weaker
than in normal epithelium or negative. In carcinomas the staining
was positive in 26 out of 45 (57,8%) intestinal, 13 out of 25
(52%) diffuse, 12 out of 13 (92,3%) mixed and 4 out of 7(57,2%)
mucinous type. Significantly higher H-score for pS2 protein was
observed in carcinomas stage III and in those with more than 3
metastatic lymph nodes (P=0.05). There was no significant correlation
of pS2 expression with clinical and pathological parameters such
as patient age or sex, tumor grade, size and location. In conclusion,
our findings indicate that: a. pS2 protein has constant expression
and disrtibution in the gastric epithelium which is probably related
to its putative physiological role in the cell renewal of gastric
mucosa, and b. high pS2 expression in gastric carcinomas may be
related to more aggressive biological behavior.
Key words: Gastric carcinoma, pS2, immunohistochemistry.
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