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. 2018 Jul 11;37(46):6041–6053. doi: 10.1038/s41388-018-0403-0

Fig. 3.

Fig. 3

MUC20 knockdown suppresses PDAC tumour growth in immunodeficient mice. a Western blots showing stable MUC20 knockdown in HPAC and HPAF-II cells. MUC20 knockdown inhibited viability in HPAC and HPAF-II cells analysed by MTT assays. Cells were stably transfected with MUC20 shRNA (sh-MUC20) or non-targeting control shRNA (sh-Control). Data are presented as mean (n = 3) ± SD. b MUC20 knockdown decreased tumour sizes (upper) and weights (lower) compared with the control group (n = 5 for each group) after four weeks of intraperitoneal injection with HPAC or HPAF-II cells in nude mice. Data are presented as mean ± SEM. c MUC20 knockdown decreased tumour sizes (upper) and weights (lower) compared with the control group (n = 6 for each group) after four weeks of subcutaneous injection with HPAF-II cells in NOD/SCID mice. d The left panel shows MUC20 knockdown decreased tumour sizes (upper) and weights (lower) compared with the control group (n = 7 for each group) after four weeks of orthotopic injection with HPAF-II cells in NOD/SCID mice. The right panel shows representative images of IHC for MUC20 in control and MUC20 knockdown tumours. Data are presented as mean ± SEM. *P < 0.05; **P < 0.01