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. 2017 Dec 1;92(3):1323–1340. doi: 10.1007/s00204-017-2115-6

Fig. 8.

Fig. 8

PARP inhibition potentiates BPDE-induced mutagenicity. An HPRT mutagenicity assay with BPDE-treated CHO cells was performed in the absence or presence of 10-µM ABT888. a Representative cell culture dishes of the HPRT assay. A BPDE dose-dependent increase in colony numbers (mutant frequency) was observed. PARP inhibition further increased BPDE-induced mutagenicity. b, c Quantification of (a) increasing concentrations of BPDE resulted in increased numbers of mutations of the HPRT gene. b BPDE treatment with concentrations of up to 500 nM. c Magnification of insert in B showing data of the low-dose range, with BPDE concentrations of up to 50 nM. When PARP activity was inhibited, an even higher mutation rate was observed. Data represent means ± SEM of four independent experiments. Statistical evaluation was performed using two-way ANOVA analysis followed by Sidak’s multiple comparison testing. *p < 0.05, **p < 0.01