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HQ, FMNT and CS significantly inhibited the ERK1/2 and PI3K-AKT signaling pathways. The protein levels of p-Erk1/2, ERK1/2, p-AKT and AKT in HT29 and Caco2 cells were detected after treatment with HQ (25, 50 and 100 mg/mL, 48 h) (A), FMNT (25, 50 and 100 μM, 48 h) (B) or CS (25, 50 and 100 μM, 48 h) (C), respectively. The data represent the mean ± SD (n = 3). * p < 0.05, ** p < 0.01 and *** p < 0.001 compared with the control group.
