P-glycoprotein (P-gly), which is responsible for the phenotypic expres
sion of multidrug resistance in cancerous tissue was stained immunohis
tochemically in previously untreated alpha-fetoprotein (AFP)-producing
(n = 20) and nonproducing gastric cancers (n = 20). P-gly, AEP, and c
arcinoembryonic antigen(CEA) were stained in formalin-fixed paraffin-e
mbedded tissue sections immunohistochemically using the monoclonal ant
ibody JSB-1, anti-AFP, and anti-CEA, respectively. DNA ploidy pattern
was determined by Fluorescence Activated Cell Sorter (FAGS) analyzer.
P-gly was significantly overexpressed in AFP producing gastric cancers
(60%) than in AFP nonproducing ones (20%) (P < 0.01). When the result
of P-gly staining was analyzed among the AFP-positive cases, P-gly po
sitivity did not emerge either as a significant prognostic factor or a
s a predictor of the metastatic potentiality of the tumor. The intrins
ic overexpression of P-gly in AFP producing gastric cancers proves its
biological and morphological similarities to hepatocellular carcinoma
. The significantly (P < 0.05) higher incidence of P-gly in diploid tu
mors indicate that expression of this phenotype might be related to th
e differentiation of the tumor. P-gly was overexpressed in AFP produci
ng gastric carcinoma and the existing drug resistance, frequent recurr
ence, and poor prognosis might be explained by presence of P-gly in th
is carcinoma. (C) 1995 Wiley-Liss, Inc.