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. 2018 Sep 3;26(6):591–598. doi: 10.4062/biomolther.2018.061

Table 1.

Antiproliferative activity of 5-Aza-CdR, FK228 and oxaliplatin in SNU-638 and SNU-719 human gastric cancer cells

SNU-638 24 h 48 h 72 h
5-Aza-CdR IC50 4.52 ± 0.27 1.01 ± 0.13 0.89 ± 0.21
R 36.1 ± 9.9 33.9 ± 4.2 30.3 ± 5.8
FK228 IC50 16.4 ± 8.9 3.72 ± 0.03 2.68 ± 0.13
R 31.7 ± 1.9 4.11 ± 4.00 2.56 ± 2.24
Oxaliplatin IC50 35.4 ± 7.3 6.63 ± 1.24 0.68 ± 0.15
R 39.6 ± 6.6 15.2 ± 18.2 13.0 ± 6.15
SNU-719 24 h 48 h 72 h
5-Aza-CdR IC50 ND 7.72 ± 0.01 5.76 ± 3.44
R 52.7 ± 1.9 48.1 ± 3.1 47.8 ± 1.9
FK228 IC50 ND 5.61 ± 0.08 3.06 ± 0.004
R 55.3 ± 4.2 25.5 ± 2.05 2.67 ± 2.03
Oxaliplatin IC50 ND 328 ± 3.9 1.24 ± 0.07
R 72.7 ± 5.07 47.8 ± 2.0 36.6 ± 0.76

Cell viability was determined using the MTS assay. IC50, the drug concentration that produces a 50% of the drug’s maximum effect following 48 or 72 h of continuous exposure; expressed in nM for FK228 and μM for 5-Aza-CdR and oxaliplatin. R, the residual unaffected fraction (resistance fraction); IC50 and R values were determined from dose-response curves analyzed using Eq. 1 and Eq. 2 (see Materials and Methods). Data are presented as the mean ± SD from at least three independent experiments. ND, not determined.