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Table 1 IC50 (µM) values and fold decrease in drug sensitivity (RI) of parental (CEM) versus resistant (CEM-VCR R and CEM/2ME2 28.8R) human acute lymphoblastic leukemia cell lines treated with microtubule targeting agents

From: N-alkylisatin-based microtubule destabilizers bind to the colchicine site on tubulin and retain efficacy in drug resistant acute lymphoblastic leukemia cell lines with less in vitro neurotoxicity

IC50 (µM) ± SDa

Resistance Index (RI)b

Compound

CEM

CEM-VCR R

CEM/2ME2-28.8R

CEM-VCR R:CEM

CEM/2ME2-28.8 R:CEM

Vincristine

0.08 (± 0.05)

8.11 (± 1.62)

0.41 (± 0.19)

101.4 < 0.05

5.1 > 0.05

Vinblastine

0.13 (± 0.06)

1.12 (± 0.16)

0.39 (± 0.13)

8.6 < 0.05

3.0 > 0.05

2-Methoxy-estradiol

0.08 (± 0.04)

4.07 (± 1.34)

8.52 (± 1.38)

50.9 < 0.05

106.5 < 0.05

Colchicine

0.32 (± 0.21)

1.01(± 0.36)

0.56 (± 0.19)

3.2 < 0.05

1.8 > 0.05

Paclitaxel

0.15 (± 0.09)

1.11 (± 0.36)

0.25 (± 0.12)

7.4 < 0.05

1.7 > 0.05

HMB-isatin

1.02 (± 0.32)

1.07 (± 0.37)

1.29 (± 0.41)

1.0 > 0.05

1.3 > 0.05

I4M-isatin

1.07 (± 0.44)

1.26 (± 0.19)

1.16 (± 0.46)

1.2 > 0.05

1.1> 0.05

N2M-isatin

0.36 (± 0.19)

0.49 (± 0.36)

0.46 (± 0.32)

1.4 > 0.05

1.3 > 0.05

  1. aValues are the mean of three independent experiments, performed in triplicate (n = 9) ± SD
  2. bThe RI was calculated to determine the degree of acquired resistance of each cell line to the various drug treatments and was determined using the following equation:\(RI = \frac{{IC50 \left( {resistant\,subline} \right)}}{{IC50 \left( {sensitive\,subline} \right)}}\). P-values < 0.05 were considered significant