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. 2020 Jan 31;39(13):2724–2740. doi: 10.1038/s41388-020-1178-7

Fig. 5. Effects of EPHA2 knockdown on gastric cancer cells in vitro and in vivo.

Fig. 5

a Western blots showing EPHA2 knockdown in AGS and MKN45 cells. b Cell viability was not significantly affected by EPHA2 knockdown in AGS and MKN45 cells analyzed by MTT assays. Cells were transfected with two independent siRNAs (si-EPHA2-1 and si-EPHA2-2) or nontargeting control siRNA (si-Control). Data are presented as mean (n = 3) ± SD. c Cell migration was analyzed using transwell migration assays. Data are presented as mean (n = 3) ± SD. *p < 0.05; **p < 0.01. d Cell invasion was analyzed using Matrigel invasion assays. Data are presented as mean (n = 3) ± SD. *p < 0.05. e Western blots showing stable EPHA2 knockdown in AGS and MKN45 cells. f Tumor sizes (left panel) and weights (right panel) were not significantly affected by EPHA2 knockdown in NOD/SCID mice subcutaneously injected with AGS cells. Mice were sacrificed at day 45 (n = 5 for each group). This experiment was conducted once. g Tumor sizes (left panel) and weights (right panel) were not significantly affected by EPHA2 knockdown in NOD/SCID mice subcutaneously injected with MKN45 cells. Mice were sacrificed at day 30. (n = 5 for each group) This experiment was conducted once. h EPHA2 knockdown decreased lung metastasis in NOD/SCID mice intravenously injected with AGS cells. Numbers of tumor nodules in lungs are shown as means ± SD. *p< 0.05. This experiment was conducted once. i Representative images of tumor formation in NOD/SCID mice intraperitoneally injected with MKN45 cells. Mice were sacrificed at day 30. Blue arrowheads indicate tumor nodules. j Statistical results of NOD/SCID mice intraperitoneally injected with MKN45 cells. EPHA2 knockdown significantly decreased numbers of tumor nodules (left panel) and total tumor weights (right panel). *p < 0.05. This experiment was conducted once. All statistical data were analyzed and obtained through Student’s t test.