We attempted to suppress glucose transporter 1 (GLUT1) expression by transf
ecting MKN45 cells with cDNA for antisense GLUT1. Glucose transport was: si
gnificantly decreased in cells with antisense GLUT1 compared with wild-type
cells or cells with vector, alone. Suppression of GLUT 1 mRNA resulted in
a decreased number of cells in the S phase. This was accompanied by overexp
ression of p21 protein. Tumorigenicity in the nude mice injected with antis
ense GLUT1 expressing cells was significantly slower than in those with wil
d-type MKN45 cells. These results suggest that antisense GLUT1 mRNA inhibit
s tumor growth through a G(1) arrest and that expression of antisense GLUT1
mRNA via gene therapy can be used as a tool in the treatment of cancer. (C
) 2000 Published by Elsevier Science Ireland Ltd. All rights reserved.