Table 1.
all patients | p53 wild type | |||||||
p53 codon 72 Arg/Arg | p53 codon 72 Pro/Pro | p53 codon 72 Arg/Pro | p | p53 codon 72 Arg/Arg | p53 codon 72 Pro/Pro | p53 codon 72 Arg/Pro | p | |
γ-irradiation (% surviving cells) |
36.3 ± 4.7 (n = 49) |
50.0 ± 10.1 (n = 7) |
24.2 ± 4.8 (n = 26) |
0.099 | 30.6 ± 4.8 (n = 39) |
54.7 ± 13.4 (n = 5) |
22.9 ± 4.9 (n = 25) |
0.14 |
log10 LC90 chlorambucil | 0.73 ± 0.07 (n = 78) |
0.76 ± 0.19 (n = 9) |
0.62 ± 0.08 (n = 49) |
0.63 | 0.6 ± 0.08 (n = 61) |
0.76 ± 0.22 (n = 7) |
0.57 ± 0.08 (n = 46) |
0.70 |
log10 LC90 mafosfamide | 0.32 ± 0.05 (n = 75) |
0.37 ± 0.12 (n = 9) |
0.21 ± 0.05 (n = 47) |
0.39 | 0.3 ± 0.06 (n = 59) |
0.38 ± 0.16 (n = 7) |
0.21 ± 0.05 (n = 44) |
0.42 |
log10 LC90 fludarabine | 0.18 ± 0.08 (n = 78) |
0.13 ± 0.18 (n = 9) |
-0.32 ± 0.1 (n = 49) |
0.32 | 0.11 ± 0.1 (n = 61) |
0.22 ± 0.23 (n = 7) |
-0.06 ± 0.01 (n = 46) |
0.28 |
log10 LC90 cladribine | -0.76 ± 0.1 (n = 78) |
-0.85 ± 0.18 (n = 9) |
-1.0 ± 0.11 (n = 49) |
0.10 | -0.89 ± 0.1 (n = 61) |
-0.79 ± 0.22 (n = 7) |
-1.04 ± 0.11 (n = 46) |
0.22 |
log10 LC90 vincristine | 0.13 ± 0.1 (n = 55) |
0.01 ± 0.27 (n = 8) |
-0.22 ± 0.11 (n = 39) |
0.71 | -0.14 ± 0.11 (n = 40) |
0.05 ± 0.33 (n = 6) |
-0.25 ± 0.11 (n = 36) |
0.59 |
log10 LC90 doxorubicin | -0.55 ± 0.04 (n = 78) |
-0.52 ± 0.06 (n = 9) |
-0.61 ± 0.05 (n = 49) |
0.64 | -0.55 ± 0.05 (n = 61) |
-0.49 ± 0.07 (n = 7) |
-0.63 ± 0.05 (n = 46) |
0.35 |
log10 LC90 methylprednisolone | 0.99 ± 0.14 (n = 78) |
1.36 ± 0.45 (n = 9) |
0.95 ± 0.18 (n = 48) |
0.70 | 0.99 ± 0.16 (n = 61) |
1.52 ± 0.47 (n = 7) |
0.95 ± 0.18 (n = 45) |
0.57 |
For the cytostatic drugs (chlorambucil, mafosfamide, fludarabine, cladribine, vincristine, doxorubicin or methylprednisolone) log10 LC90 concentrations were compared. In case of ionizing γ-irradiation with a fixed dose of 2 Gy, percentages of surviving cells were compared. p53 WT: wild type p53 gene. Mean +/- SEM is given. Statistical significance was calculated by means of the Kruskal-Wallis test.