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. Author manuscript; available in PMC: 2009 Sep 1.
Published in final edited form as: Mol Pharmacol. 2008 Jun 5;74(3):863–871. doi: 10.1124/mol.107.043349

Table 1.

Effect of FdUrd on the sensitivity of HCT 116 0–1, HCT116 1–2 and SW620 cells to ionizing radiation.

MLH1 expression Cell line [FdUrd] Radiation Enhancement Ratio D-bar (no drug)
Inactivated HCT116 0–1 0.25µM (IC10) 1.8 ± 0.33
3.5 µM (IC50) 1.8 ± 0.28 3.1 ± 0.19
Wildtype HCT116 1–2 0.125 µM (IC10) 1.2 ± 0.03
0.75 µM (IC50) 1.1 ± 0.10 2.9 ± 0.14
3.5 µM (IC90) 1.4 ± 0.10*
Suppressed HCT116 1–2 + 0.75 µM 1.5 ± 0.06* 2.8 ± 0.21*
shRNA-MLH1 3.5 µM 1.7 ± 0.13*
2.8 ± 0.13*
Wildtype HCT116 1–2 +
shRNA-non-
specific
0.75 µM 1.1 ± 0.10*
wild-type SW620 0.35 µM (IC50) 1.2 ± 0.12
3.5 µM (IC90) 1.4 ± 0.04 2.2 ± 0.14
Suppressed SW620 + shRNA-MLH1 0.35 µM 1.6 ± 0.10 2.3 ± 0.24
3.5 µM 1.8 ± 0.03*
Wildtype SW620 + shRNA-non-specific 0.35 µM 1.2 ± 0.08 2.3 ± 0.17

Radiation enhancement ratios (mean ± SE) are shown for all cell lines after a 24 hr drug incubation followed by irradiation. Sensitivity to radiation in control cells (no drug) is shown as the D-bar.

Each value is an average of at least three separate (mean ± SE), or two separate (mean ± SD*) experiments.

significantly >1 (p < 0.05)