Fig. 8: The combination of IR and MC4448 inhibitor induces DNA damage and impairs DNA repair.

A Representative immunofluorescence images of γH2AX (green, left) (n = 3 independent biological replicates) in MC4448 treated RH30 and RH4 cells 6 h post IR with 6 Gy. DAPI (blue) was used as nuclear counterstain. Scale Bar = 10 μm. Scatter plot of γH2AX average intensity per cell number (right) in MC4448 treated RH30 and RH4 cells after 6 h post IR with 6 Gy. Graph represents the mean of three independent experiments ±SEM, ANOVA one-way test. Exact p values are reported in the figure. B Analysis of DSBs accumulation by the neutral Comet assay. Representative images are reported above. RH30 and RH4 cells were treated with MC4448 and then exposed to 6 Gy of IR. After 6 h FP-RMS cells were subjected to the neutral Comet assay. In the scatter plot below, data are presented as mean tail moment ± SEM, ANOVA one-way test. Exact p values are reported in the figure. C Representative western blot (n = 2 independent biological replicates) of FP-RMS cells treated with MC4448 and IR (6 Gy). The cells were processed 6 h post IR to evaluate the effect of combination of treatments on DNA damage response. pATM (Ser 1981), total ATM, pDNA-PKcs (Thr2609), total pDNA-PKcs, Rad51, and Ku70 protein levels were detected. All protein levels were normalized on Vinculin.