Macrophage migration inhibitory factor regulates proliferation of gastric cancer cells via the PI3K/Akt pathway

Figure 5 Effects of rhMIF on the expression of p-Akt and Akt in MGC-803 cells. Cell lysates were isolated for Western blotting to detect the expression of p-Akt and Akt (A, B). A: MGC-803 cells were treated with 25, 50 and 100 μg/L rhMIF for 30 min. ^aP < 0.05 vs control group; ^cP < 0.05 vs 25 μg/L MIF group; ^eP < 0.05 vs 50 μg/L MIF group; B: MGC-803 cells were treated with 50 μg/L rhMIF at different time points (5, 15, 30 and 60 min). ^aP < 0.05 vs control group; ^cP < 0.05 vs 5 min group; ^eP < 0.05 vs 15 min and 60 min groups; C: With or without 1-h pretreatment with 25 μmol/L LY294002, MGC-803 cells were exposed to 50 μg/L rhMIF for 30 min with a vehicle control of DMSO (less than 0.1%) included, and then the expression of p-Akt and Akt was determined by Western blotting. ^aP < 0.05 vs control group; ^cP < 0.05 vs MIF group; ^eP < 0.05 vs LY+MIF group; D: The arrow symbols represent immunocytochemical staining for nuclear and cytoplasmic expression of p-Akt (original magnification, × 200) in MGC-803 cells. The results were represent as mean ± SD of three independent experiments. DMSO (the menstruum of LY294002, less than 0.1%) had little impact on the rhMIF effect.