Approximately, 2.0 × 105 Huh7 cells were seeded in 12-well plates and cultured until complete adherence. After that, actinomycin D (Abcam, United States) was added to the culture media at a final concentration of 2 μg/ml. Then, the cells in wells were collected for RNA extraction at 0, 3, 6, 12, and 24 h, respectively. The RNA samples were subjected to reverse transcription and RT-qPCR systems.
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