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. Author manuscript; available in PMC: 2021 Dec 13.
Published in final edited form as: Curr Med Chem. 2020;27(24):4016–4038. doi: 10.2174/0929867326666190228120908

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
a

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].

b

1 μM entinostat

c

2.5 μM entinostat.

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