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. 2017 Sep 28;14(6):6477–6484. doi: 10.3892/ol.2017.7095

Table II.

Effects of HNF-4α on drug sensitivities of GC cells.

IC50 values, µg/ml

Cell line ADR 5-Fu CDDP VCR MMC
SGC7901 0.52±0.05 3.11±0.22 1.63±0.21 0.25±0.01 1.39±0.16
SGC7901-Ctrl 0.61±0.11 2.89±0.34 1.93±0.28 0.29±0.08 1.56±0.23
SGC7901-HNF4α 1.58±0.29a 6.98±0.73a 4.16±0.52a 1.73±0.31a 4.55±0.67a
SGC7901/VCR 5.44±0.47 9.17±1.15 7.65±0.94 5.86±0.69 8.22±1.03
SGC7901/VCR-siCtrl 6.21±0.79 10.83±1.57 7.02±0.86 6.29±0.88 9.03±1.27
SGC7901/VCR-siHNF4α 2.95±0.38b 8.21±0.93b 5.14±0.78b 3.46±0.52b 6.11±0.94b

HNF4α was overexpressed in SGC7901 cells and suppressed in SGC7901/VCR cells with lentiviruses expressing HNF-4α or its specific small interfering RNA (siHNF4α). The sensitivity of SGC7901 and SGC7901/VCR cells, and their variants, was determined in vitro using an MTT assay. SGC7901-Ctrl and SGC7901/VCR-siCtrl cells were infected with control lentiviruses.

a

P<0.01 vs. SGC7901 and SGC7901-Ctrl.

b

P<0.01 vs. SGC7901/VCR and SGC7901/VCR-siCtrl. Results are representative of 3 independent experiments. IC50, half-maximal inhibitory concentration; Ctrl, control; ADR, Adriamycin; 5-Fu, 5-fluorouracil; CDDP, cisplatin; VCR, vincristine; MMC, mitomycin; HNF-4α, hepatocyte nuclear factor-4α.