An MTT assay was carried out to examine cell viability to determine HCC cell proliferation. The cells (5×103 cells/ml) treated with different transfection were planted in 96-well plates and incubated for 48 h at 37°C with 5% CO2. Then, we added MTT reagent (20 ml) to each well at 0, 1, 2, 3 and 4 days followed by incubation for another 4 h. Dimethyl sulfoxide (150 ml) was added to dissolve the crystallization. The absorbance value of cells was measured at 490 nm using enzyme-linked immunoassay.
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