M. Nozue et al., 5-FU DOSE-DEPENDENCY IN MTX S-FU SEQUENTIAL THERAPY ASSESSED BY IN-VITRO ASSAY USING GASTRIC-CANCER CELL-LINES/, Oncology Reports, 2(5), 1995, pp. 737-740
The sequential administration of methotrexate (MTX) and 5-fluorouracil
(5-FU) (MTX/5-FU therapy) on gastric cancers has shown higher respons
e rates than standard chemotherapy. The response rate of these cancers
, however, still showed from 18 to 48%. The purpose of this study was
to determine the appropriate interval time and doses of MTX/5-FU thera
py using a panel of 4 cell lines originated from the poorly-differenti
ated gastric cancers. The (4,5-dimethylthiazol-2-yl)-2,5-diphenyltetra
zolium bromide (MTT) assay was used as the chemosensitivity test. The
sequential administration of MTX and 5-FU inhibited the growth of 2 ce
ll lines more than 5-FU alone. In one cell line (GCIY), it inhibited t
he growth 6 times, and the longest interval time (6 h) was the most ef
fective. In the other cell line (KATOIII), it inhibited growth 3 times
, and the shortest interval time (O h) was the most effective. The gro
wth inhibition in these cases did not depend on the dose of MTX (0.01
mu g/ml to 100 mu g/ml), but on the dose of 5-FU. In conclusion, 2 out
of 4 cell lines showed a synergic effect between MTX and 5-FU. While
the appropriate interval time between the two drugs varied between two
cell lines, 5-FU dose was more critical than that of MTX. If 5-FU dos
e were to be increased in future trials with MTX, its efficacy might b
e higher. This model should also be good to screen other anti cancer d
rugs combined with MTX/5-FU therapy.