TY - JOUR
T1 - Plasma-activated saline hyperthermic perfusion-induced pyroptosis boosts peritoneal carcinomatosis immunotherapy
AU - Qi, Miao
AU - Zhao, Xinyi
AU - Fan, Runze
AU - Lin, Jiao
AU - Li, Zhuo
AU - Liu, Na
AU - Sun, Xuejun
AU - Xu, Dehui
AU - Zheng, Jianbao
AU - Liu, Dingxin
AU - Zhou, Renwu
AU - Rong, Mingzhe
AU - Ostrikov, Kostya (Ken)
N1 - Publisher Copyright:
© 2025
PY - 2025/3/16
Y1 - 2025/3/16
N2 - Peritoneal carcinomatosis (PC) is a common metastatic cancer with limited treatment options. Herein, we present a novel strategy for the combined treatment of PC involving plasma-activated saline (PAS) and hyperthermic intraperitoneal perfusion. PAS revealed a strong cytotoxic effect because of reactive oxygen species (ROS) in two-dimensional cultures and three-dimensional tumor spheroids of PC-related cell lines. Notably, PAS induced Gasdermin E (GSDME)-dependent pyroptosis and immunogenic cell death in vitro. PAS-enhanced hyperthermic intraperitoneal perfusion (PE-HIP) increased the number of CD3+, CD4+ and CD8+ T cells, while decreased the number of regulatory T cells, indicating that PAS stimulated T cell-based immune responses in vivo. Moreover, PE-HIP significantly inhibited tumor growth and improved survival in a PC-mice model, with no significant toxic side effects. Meanwhile, vaccination with PAS-induced cell pyroptosis activated systemic antitumor immunity to prevent subcutaneous tumor growth. Overall, PE-HIP can serve as a new approach for PC treatment by ROS-assisted cancer immunotherapy.
AB - Peritoneal carcinomatosis (PC) is a common metastatic cancer with limited treatment options. Herein, we present a novel strategy for the combined treatment of PC involving plasma-activated saline (PAS) and hyperthermic intraperitoneal perfusion. PAS revealed a strong cytotoxic effect because of reactive oxygen species (ROS) in two-dimensional cultures and three-dimensional tumor spheroids of PC-related cell lines. Notably, PAS induced Gasdermin E (GSDME)-dependent pyroptosis and immunogenic cell death in vitro. PAS-enhanced hyperthermic intraperitoneal perfusion (PE-HIP) increased the number of CD3+, CD4+ and CD8+ T cells, while decreased the number of regulatory T cells, indicating that PAS stimulated T cell-based immune responses in vivo. Moreover, PE-HIP significantly inhibited tumor growth and improved survival in a PC-mice model, with no significant toxic side effects. Meanwhile, vaccination with PAS-induced cell pyroptosis activated systemic antitumor immunity to prevent subcutaneous tumor growth. Overall, PE-HIP can serve as a new approach for PC treatment by ROS-assisted cancer immunotherapy.
KW - Hyperthermic intraperitoneal perfusion
KW - Immunotherapy
KW - Peritoneal carcinomatosis
KW - Plasma-activated saline
KW - Pyroptosis
UR - https://www.scopus.com/pages/publications/85217954240
U2 - 10.1016/j.freeradbiomed.2025.02.002
DO - 10.1016/j.freeradbiomed.2025.02.002
M3 - 文章
C2 - 39914684
AN - SCOPUS:85217954240
SN - 0891-5849
VL - 230
SP - 177
EP - 189
JO - Free Radical Biology and Medicine
JF - Free Radical Biology and Medicine
ER -