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©2009 The WJG Press and Baishideng.
World J Gastroenterol. Nov 28, 2009; 15(44): 5541-5548
Published online Nov 28, 2009. doi: 10.3748/wjg.15.5541
Published online Nov 28, 2009. doi: 10.3748/wjg.15.5541
Figure 2 Effects of rhMIF and LY294002 on cell cycle of MGC-803 cells.
With or without 1-h pretreatment with 25 μmol/l LY294002, MGC-803 cells were exposed to 50 μg/L rhMIF for 24 h. A vehicle control of DMSO (less than 0.1%) was included. Cell lysates were prepared for the cell cycle detection. The cell cycle distribution was analyzed using an Eics-XL II flow cytometer. A: Control; B: MIF group; C: LY+MIF group; D: DMSO+MIF group; E: LY group; F: Quantification of G1/S viability(%) analysis of MGC-803 cells. Data were represented as mean ± SD of three independent experiments. aP < 0.05 vs control group; cP < 0.05 vs MIF group; eP < 0.05 vs LY+MIF group. DMSO (the menstruum of LY294002, less than 0.1%) had little impact on the rhMIF effect.
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Citation: Li GQ, Xie J, Lei XY, Zhang L. Macrophage migration inhibitory factor regulates proliferation of gastric cancer cells
via the PI3K/Akt pathway. World J Gastroenterol 2009; 15(44): 5541-5548 - URL: https://www.wjgnet.com/1007-9327/full/v15/i44/5541.htm
- DOI: https://dx.doi.org/10.3748/wjg.15.5541