Compound 16 induces EZH2 degradation in a time- and
concentration-dependent manner. (A) Western blots of EZH2, SUZ12,
EED, and H3K27me3 post-treatment of MDA-MB-453 cells with DMSO (48
h) or compound 16 (1 μM) at the indicated time
points. β-Actin and H3 were used as the loading controls. (B)
Quantification of EZH2 blots in (A) and their replicates. (C) Western
blots of EZH2, SUZ12, and EED post-treatment of MDA-MB-453 cells with
DMSO or compound 16 at the indicated concentrations for
48 h. β-Actin was used as the loading control. (D) Quantification
of EZH2 blots in (C) and their replicate. (E) DC50 curve
of 16, generated using the data in (D).