Galactosyltransferase (GalTase) has been discovered on a variety of ce
lls where it is believed to be involved in cell-cell adhesion and cell
-substratum adhesion as well as in metastasis of carcinoma cells. This
immunohistochemical study was undertaken to identify the topography a
nd the cellular distribution of GalTase in normal prostatic tissue, be
nign prostatic hyperplasia (11 cases), and prostatic carcinoma (26 cas
es). Immunoreactive GalTase was found to be exclusively associated wit
h carcinoma cells and with premalignant epithelial cells in prostatic
hyperplasia. In highly differentiated carcinomas, most of the carcinom
a cells are positive for GalTase, whereas in poorly differentiated tum
ors, GalTase immunoreactivity was restricted to a subset of carcinoma
cells with obviously invasive behavior At the cellular level, GalTase
was localized in the cytoplasm and at the cell membrane. In sections o
f normal prostatic tissue, as well as in unaltered acini of prostatic
hyperplasic tissue, GalTase was not expressed. Fibroblasts, smooth mus
cle cells, and endothelial cells of the prostatic stroma were also con
sistently negative. With the use of immunoblots, we could confirm the
presence of GalTase with a molecular mass of 45 kDa in the extracts of
benign prostatic hyperplasic tissue and in prostatic carcinoma tissue
bur not in normal prostatic tissue. The results of our immunohistoche
mical study suggest that GalTase is a valuable marker to diagnose neop
lastic transformation in prostatic tissue.