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. 2017 Aug 8;9(11):9608–9617. doi: 10.18632/oncotarget.20033

Figure 4. Knockdown of any of several key SWI/SNF subunits sensitizes human pancreatic ductal epithelial cells to oxaliplatin.

Figure 4

(A) siRNA knockdown of SMARCA2, ARID1A and ARID1B in HPDE cells, confirmed by western blot, compared to non-targeting control (NTC); GAPDH serves as a loading control. (B) Bar graph summarizing fold-reductions in IC50 with knockdown of SMARCA4 (from Figure 1D), SMARCA2, ARID1A, and ARID1B (vs. NTC), for oxaliplatin. (CE) Dose-response curves comparing HPDE cell viability following knockdown of (C) SMARCA2, (D) ARID1A, and (E) ARID1B (vs. NTC), for oxaliplatin. IC50 values indicated.