Temozolomide-based sonodynamic therapy induces immunogenic cell death in glioma

被引:17
|
作者
Zhou, Yan [1 ]
Jiao, Jiji [1 ]
Yang, Rongyan [2 ]
Wen, Binli [1 ]
Wu, Qiaoli [3 ]
Xu, Lixia [1 ,3 ,4 ]
Tong, Xiaoguang [1 ,3 ,4 ]
Yan, Hua [1 ,3 ,4 ]
机构
[1] Tianjin Med Univ, Clin Coll Neurol Neurosurg & Neurorehabil, Tianjin 300350, Peoples R China
[2] Nankai Univ, Coll Environm Sci & Engn, Tianjin 300350, Peoples R China
[3] Tianjin Huanhu Hosp, Tianjin Neurosurg Inst, Tianjin Key Lab Cerebral Vasc & Neurodegenerat Dis, Tianjin 300350, Peoples R China
[4] Tianjin Huanhu Hosp, Tianjin Neurosurg Inst, Tianjin Key Lab Cerebral Vasc & Neurodegenerat Dis, 6 Jizhao Rd, Tianjin 300350, Peoples R China
基金
中国国家自然科学基金;
关键词
Temozolomide; Immunogenic cell death; Sonodynamic therapy; Glioblastoma; Nanoliposome; ENDOPLASMIC-RETICULUM STRESS; ADJUVANT TEMOZOLOMIDE; SERINE SYNTHESIS; GLIOBLASTOMA; ENHANCE; INFLAMMASOME; RADIOTHERAPY; CONCOMITANT; ULTRASOUND; EXPRESSION;
D O I
10.1016/j.clim.2023.109772
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: In our previous study, we found for the first time that temozolomide (TMZ), the first-line chemo-therapeutic agent for glioblastoma (GBM), can generate a large amount of reactive oxygen species (ROS) under ultrasound irradiation. Sonodynamic therapy (SDT) using TMZ as the sonosensitizer produced more potent antitumor effects than TMZ alone. Here, we further evaluate the effects of TMZ-based SDT on subcellular structures and investigate the immunogenic cell death (ICD)-inducing capability of TMZ-based SDT. Methods: The sonotoxic effects of TMZ were explored in LN229 and GL261 glioma cells. The morphology of endoplasmic reticulum and mitochondria was observed by transmission electron microscopy. The nuclear DNA damage was represented by gamma-H2AX staining. Bone marrow-derived dendritic cells (BMDCs) were employed to assess ICD-inducing capability of TMZ-based SDT. A cyclic arginine-glycine-aspartic (c(RGDyC))-modified nanoliposome drug delivery platform was used to improve the tumor targeting of SDT. Results: TMZ-based SDT had a greater inhibitory effect on glioma cells than TMZ alone. Transmission electron microscopy revealed that TMZ-based SDT caused endoplasmic reticulum dilation and mitochondrial swelling. In addition, endoplasmic reticulum stress response (ERSR), nuclear DNA damage and mitochondrial permeability transition pore (mPTP) opening were promoted in TMZ-based SDT group. Most importantly, we found that TMZ-based SDT could promote the "danger signals" produced by glioma cells and induce the maturation and acti-vation of BMDCs, which was associated with the mitochondrial DNA released into the cytoplasm in glioma cells. In vivo experiments showed that TMZ-based SDT could remodel glioma immune microenvironment and provoke durable and powerful anti-tumor immune responses. What's more, the engineered nanoliposome vector of TMZ conferred SDT tumor targeting, providing an option for safer clinical application of TMZ in combination with SDT in the future. Conclusions: TMZ-based SDT was capable of triggering ICD in glioma. The discovery of TMZ as a sonosensitizer have shown great promise in the treatment of GBM.
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页数:14
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