糖酵解
癌症研究
免疫疗法
医学
癌症免疫疗法
奥沙利铂
癌症
转移
热疗
化疗
光热治疗
获得性免疫系统
活性氧
免疫原性细胞死亡
黑色素瘤
免疫检查点
联合疗法
先天免疫系统
化学
伊立替康
药理学
免疫系统
炎症
程序性细胞死亡
癌细胞
巴基斯坦卢比
DNA损伤
附带损害
靶向治疗
细胞因子
细胞毒性
作者
Henan Xu,Yuxin Jiang,Ruohao Zhang,Daguang Wang,Jing Feng,Hongjie Zhang
标识
DOI:10.1016/j.mtbio.2026.102790
摘要
-mediated Fenton-like reaction, OXP, and mPTT also induce immunogenic cell death (ICD) to boost adaptive immunity, as well as activate the cGAS-STING pathway through tumor DNA damage to reinforce innate immunity. The activation of both adaptive and innate immune responses triggers a potent antitumor immune reaction, which, combined with chemotherapy and enhanced mPTT, significantly suppresses tumor growth, metastasis and recurrence. This strategy not only enhances the targeting of chemotherapeutic drugs but also provides new possibilities for expanding the field of immunotherapy in gastric cancer by regulating tumor metabolism and enhancing mPTT.
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