De. Burstein et al., GLUT1 GLUCOSE-TRANSPORTER - A HIGHLY SENSITIVE MARKER OF MALIGNANCY IN BODY CAVITY EFFUSIONS, Modern pathology, 11(4), 1998, pp. 392-396
Malignant cells exhibit increased rates of glycolysis and glucose upta
ke, and several types of cancer have been reported to overexpress the
GLUT1 glucose transporter. The diagnosis of malignancy in body cavity
effusions remains a dilemma in certain cases, despite recent progress
in diagnostic immunocytochemistry. We used immunostaining to detect th
e facilitative glucose transporter, GLUT1, in cytologic preparations o
f body cavity effusions and washes. With the use of standard avidin-bi
otin immunostaining for GLUT1, we examined cell blocks of body cavity
effusions or washings from 31 carcinomas, 1 lymphoma, and 25 benign ef
fusions or washes. GLUT1 staining occurred in the malignant cell popul
ation in 29 (93.5%) of 31 carcinomatous effusions or washes. The chara
cteristic staining pattern. consisted of dense, linear staining of the
plasma membrane, with accentuation at cell-cell borders, wills or wit
hout cytoplasmic staining. Erythrocytes showed positive GLUT1 membrane
staining, consistent with previous reports. Of 25 benign effusions, 2
0 were nonstaining (excepting erythrocytes), and 5 contained rare sing
le mesothelial cells, with equivocal to very weak membrane staining. S
taining of these cells was readily distinguishable from the characteri
stic strong staining of malignant cells, and these cells were easily d
istinguished from tumor cells by their benign morphologic characterist
ics. At least three of these latter five specimens were from patients
with cirrhosis, In all of the other eases, mesothelial cells, histiocy
tes, and other inflammatory cells did not stain. These findings sugges
t that GLUT1 immunostaining could be useful in diagnostic cytopatholog
y. The findings also suggest that enhanced glycolysis, which requires
increased glucose transport, might be a survival adaptation for tumor
cells in effusions, a significant number of which are hypoxic.