Cyclosporin A, an potent immunosuppressant, has been known to be one o
f the modulators of drug resistance as well as a cytostatic drug. Desp
ite many attempts to basic or clinical application of cyclosporin A, t
here are few reports on the inhibition of brain tumor cells. In the pr
esent experiment, the possibility of cyclosporin A as synergic adjuvan
t was investigated by MTT assay, [H-3] thymidine uptake and through fl
owcytometric anaysis. Sole treatment of cyclosporin A on the CRT and C
H235-MG glioma cell line revealed dose dependent cytotoxicity within a
range of tested dose. Combined treatment of cyclosporin A with ACNU,
BCNU and hydroxyurea on various glioma cancer cell line led to a signi
ficant synergistic cytotoxicity as well as inhibition of DNA synthesis
with dose-dependency. In addition, cyclosporin A alone or combined tr
eatment caused discernible changes of cell cycle in the tested cells.
These data provide that cyclosporin A could potentiate the effect of n
itrosourea compounds in vitro on human glioma cells.