Copyright: ©Author(s) 2026.
World J Gastroenterol. Apr 21, 2026; 32(15): 115226
Published online Apr 21, 2026. doi: 10.3748/wjg.v32.i15.115226
Published online Apr 21, 2026. doi: 10.3748/wjg.v32.i15.115226
Figure 2 Combinatorial therapy with high-frequency irreversible electroporation, BMS-1, and R848 prolongs survival and inhibits tumor growth in hepatoma 22 subcutaneous tumor-bearing mice.
A: Schematic of the hepatoma 22 subcutaneous tumor model and experimental treatment timeline; B: Kaplan-Meier survival curves across the different treatment groups (n = 8); C: Tumor growth kinetics presented as dynamic volume curves over the observation period (n = 8); D: Comparison of subcutaneous tumor volumes measured on day 21 post-treatment (n = 8). bP < 0.01, cP < 0.001, and dP < 0.0001. i.p.: Intraperitoneal; i.t.: Intratumoral; H-FIRE: High-frequency irreversible electroporation; H22: Hepatoma 22.
- Citation: Huang SM, Zhang XB, Li J, Zhang GH, Zhang X, Wei YT, Sun H, Ma L, Wang ZJ, Yao DX, Shi HJ, Wang T, Xiao YY. High-frequency irreversible electroporation synergizes with PD-1/PD-L1 inhibitor BMS-1 and TLR7/8 agonist R848 to potentiate liver cancer antitumor immunity. World J Gastroenterol 2026; 32(15): 115226
- URL: https://www.wjgnet.com/1007-9327/full/v32/i15/115226.htm
- DOI: https://dx.doi.org/10.3748/wjg.v32.i15.115226