Skip to main content
. 2019 Dec 13;34(5):1315–1328. doi: 10.1038/s41375-019-0677-4

Fig. 5. Effect of G2/M arrest inhibitors on cell proliferation and on cell cycle.

Fig. 5

Cell proliferation (flow cytometry) and CDK1 phosphorylation at Tyr15 and Thr14 (western blotting) were determined in a Rec-1, and b OCI-Ly8 cells during and after exposure to 0 (NT) and 6 MBq/mL 177Lu-lilotomab alone, or with 1 µM MK-1775 (WEE-1 inhibitor) or 1 µM PD-166285 (WEE-1 and MYT-1 inhibitor). Proliferation was calculated as the percentage of the value in nontreated cells (left black bar) set to 100%. Data are the mean ± SD of three independent experiments in triplicate (*p < 0.05). c The percentage of Ramos, DOHH2, Rec-1, and OCI-Ly8 cells in the G2/M cell cycle upon exposure or not (NT) to 177Lu-lilotomab, 177Lu-lilotomab + 1 µM MK-1775 (WEE-1 inhibitor), or PD-166285 (WEE-1 and MYT-1 inhibitor) was determined. Data are the mean ± SD of three independent experiments in triplicate.