Fig. 2: Cytotoxicity and interaction of HDACis and TLR7as in ovarian carcinoma cells. | Communications Biology

Fig. 2: Cytotoxicity and interaction of HDACis and TLR7as in ovarian carcinoma cells.

From: Enhanced antitumoral activity of TLR7 agonists via activation of human endogenous retroviruses by HDAC inhibitors

Fig. 2

a The cytotoxicity of the HDACis vorinostat and romidepsin in SKOV3WT and OvCa236 primary ovarian carcinoma cells was determined using the MTT proliferation assay after 72 h of drug exposure. Vorinostat and romidepsin are very cytotoxic in ovarian carcinoma cells (IC50 ~ 4 nM). b The TLR7as imiquimod and vesatolimod were tested in the same manner as the HDACis proved less cytotoxic in these carcinoma cell types, with IC50 values between 23 and 32 µM. These values were employed as reference in all subsequent biochemical experiments. The graphs are representative of n = 5 experiments. c HDACi/TLR7a interaction was analysed using isobolographic methods in SKOV3WT and OvCa236 primary ovarian carcinoma cells isolated from ascites. The combination of HDACis and TLR7as produces a synergistic effect regardless of pairing (green arrows). Results are representative of n = 5 experiments.

Back to article page