In order to determine if telomerase activity contributes to the growth of g
lioma cells, we constructed an anti-telomerase vector to suppress telomeras
e expression in glioma cells. The human telomerase (hTR)-antisense vector s
howed a significant suppression effect. However it did not appear to induce
cell death as a stable population of cells survived more than two months f
ollowing transfection. These results provide evidence that reagents aimed a
t inhibiting telomerase may represent a useful strategy for suppressing the
growth of glioma cells. In addition to telomerase, another mechanism would
also maintain telomere length, thus supporting continuous cell proliferati
on.