O. Nativ et al., ANTINEOPLASTIC ACTIVITY OF PACLITAXEL ON EXPERIMENTAL SUPERFICIAL BLADDER-CANCER - IN-VIVO AND IN-VITRO STUDIES, International journal of cancer, 70(3), 1997, pp. 297-301
The effects of intravesical administration of paclitaxel (taxol) in a
bladder tumor model in mice, as well as the drug's in vitro activity o
n the same tumor cells, have been studied. Two cell lines, derived fro
m MBT-2 cells, were employed in these experiments. The T50 line (obtai
ned by many passages in mice) was much more aggressive in vivo than th
e T5 line. In vivo paclitaxel treatment for 3 days after T5 implantati
on resulted in a considerable retardation of tumor growth, whereas und
er the same conditions the T50 line was much less, although still sign
ificantly, affected. When treatment was started 1 day after tumor impl
antation, both tumor variants were affected by paclitaxel to the same
extent. The in vitro experiments utilized the MiCK assay, which allows
continuous recording of the kinetics of cell growth. These studies re
vealed a 39.8% inhibition of cell growth by 2.10(-8)M paclitaxel in th
e T50 line and a 30-fold increase in concentration had only a small ad
ditional effect on the degree of inhibition. At 2.10(-8)M paclitaxel,
growth of T5 was inhibited by 21.7%, which increased to 35.2% at 6.10(
-7)M. The treated cells displayed bundles of microtubuli, as described
for other paclitaxel-treated cells. (C) 1997 Wiley-Liss, Inc.