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Effect of Mel on the proliferation and apoptosis of HepG2 cells. A. The cells were treated with different concentrations of Mel for 24, 48 and 72 h, respectively. The cell viability measured by MTT indicated that Mel could inhibit cell proliferation, and the inhibition was increased along with the levels of Mel and treatment time (all P<0.05). B. Mel induces the apoptosis of HepG2 cells, and the induction was promoted with increasing concentration of Mel.
