SNAI2 knockdown reduces tumorigenicity and resistance to gemcitabine in spheroids from human pancreatic cancer. A‐D, Control Vector and shSNAI2 from Sph were subcutaneously transplanted into NOD‐SCID mice (105 cells, 104 cells per site), respectively. shRNA was used shSNAI2_1. n = 6. A, Macroscopic images of formed tumor. B, Number of tumor‐forming mice per total transplanted mice at 8 wk after transplantation. C, H&E staining of formed tumors. Scale bars: 100 µm. D, Tumor growth curves. Mean + SE. **P < .01. E, Flow cytometric analysis of control vector and shSNAI2 from spheroids. shRNA was used shSNAI2_1. Two parameter plots: CD44‐FITC (X axis), CD24‐PE (Y axis), Numbers represent the CD44‐positive/CD24‐positive cell ratio. Histogram: EpCAM‐PECy7 (X axis), cell count (Y axis). CD44 and CD24 double analysis was performed for the blue colored fraction of the EpCAM panel. n = 2, each. Mean + SE. *P < .05. F, The relative viability of control vector versus shSNAI2 from spheroid 96 h after treating cells with gemcitabine. Viability curves at 0, 10, 50, 100 ng/mL gemcitabine. n = 5, each. Mean + SE. **P < .01