Table 3.
HDAC inhibition of human ovarian cancer cells leads to increased expression of the mAb 376.96 defined B7-H3 epitope.a
Number of B7-H3 binding sites/cell (×104) | Entinostat/control ratio | ||
---|---|---|---|
Control | Entinostat | ||
Adherent Hey-A8 | 6.54 | 30.8b | 4.71 |
CIC Hey-A8 | 6.07 | 22.0b | 3.62 |
Adherent ES-2 | 9.48 | 55.3c | 5.83 |
CIC ES-2 | 10.4 | 27.7c | 2.66 |
Adherent SKOV3.ip1 | 16.7 | 25.1c | 1.50 |
CIC SKOV3.ip1 | 19.7 | 38.3c | 1.94 |
Adherent SKOV3-TR | 24.4 | 40.0c | 1.64 |
CIC SKOV3-TR | 13.7 | 27.7c | 2.02 |
Scatchard results from binding assays with 99mTc-376.96 and ovarian cancer cell lines cultured with or without entinostat for 3 days. At 24 h after seeding ovarian cancer cell lines in culture as adherent monolayers (Adherent) or as non-adherent tumorspheres with enriched CIC characteristics (CIC), vehicle (control) or entinostat at the indicated concentration was added to the cells for 3 days. After the 3-day treatment period, adherent monolayers or dissociated CICs in suspension were incubated with dilutions of 99mTc-376.96 with or without unlabeled mAb 376.96 as a blocking agent for 1 h at 37 °C in Scatchard cell binding assays. The data were analyzed as previously described to determine the number of binding sites per cell [25].
1 μM entinostat
2.5 μM entinostat.