Yun-Shi Zhi , Tie Chen , Bin-Fa Liang , Shan Jiang , Da-Hong Yao , Zhen-Dan He , Chen-Yang Li , Liang He , Zheng-Yin Pan
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Mechanistic studies have revealed that complex <strong>Ir3</strong> induces characteristics of damage-related molecular patterns (DAMPs) in MDA-MB-231 breast cancer cells under light conditions. These include cell-surface calreticulin (CRT) eversion, extracellular high mobility group box 1 (HMGB1) and ATP release, accompanied by ER stress and increased reactive oxygen species (ROS). Consequently, complex <strong>Ir3</strong> promotes dendritic cell maturation and antigen presentation under light conditions, fully activates T cell-dependent immune response <em>in vivo</em>, and ultimately eliminates distant tumors while destroying primary tumors. In conclusion, immune regulation and targeted intervention mediated by metal complexes represent a new and promising approach to tumor therapy. This provides an effective strategy for the development of combined targeted therapy and immunotherapy.</p></div>","PeriodicalId":364,"journal":{"name":"Journal of Inorganic Biochemistry","volume":null,"pages":null},"PeriodicalIF":3.8000,"publicationDate":"2024-08-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Endoplasmic reticulum-targeted iridium(III) photosensitizer induces pyroptosis for augmented tumor immunotherapy\",\"authors\":\"Yun-Shi Zhi , Tie Chen , Bin-Fa Liang , Shan Jiang , Da-Hong Yao , Zhen-Dan He , Chen-Yang Li , Liang He , Zheng-Yin Pan\",\"doi\":\"10.1016/j.jinorgbio.2024.112695\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>An ideal tumor treatment strategy involves therapeutic approaches that can enhance the immunogenicity of the tumor microenvironment while simultaneously eliminating the primary tumor. 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Consequently, complex <strong>Ir3</strong> promotes dendritic cell maturation and antigen presentation under light conditions, fully activates T cell-dependent immune response <em>in vivo</em>, and ultimately eliminates distant tumors while destroying primary tumors. In conclusion, immune regulation and targeted intervention mediated by metal complexes represent a new and promising approach to tumor therapy. 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引用次数: 0
摘要
理想的肿瘤治疗策略包括既能增强肿瘤微环境的免疫原性,又能消除原发肿瘤的治疗方法。据报道,一种针对内质网(ER)的胆酸修饰铱(III)(Ir3)光敏剂对三阴性乳腺癌(MDA-MB-231)具有强效的 I 型和 II 型光动力治疗效果。这种光敏剂可通过光动力手段诱导由 gasdermin E(GSDME)介导的热跃迁细胞死亡,并增强肿瘤免疫疗法。机理研究发现,在光照条件下,复合物 Ir3 可诱导 MDA-MB-231 乳腺癌细胞出现损伤相关分子模式(DAMPs)的特征。其中包括细胞表面钙网蛋白(CRT)反转、细胞外高迁移率基团框 1(HMGB1)和 ATP 释放,同时伴有 ER 应激和活性氧(ROS)增加。因此,复合体 Ir3 在光照条件下促进树突状细胞成熟和抗原递呈,充分激活体内 T 细胞依赖性免疫反应,最终在摧毁原发肿瘤的同时消除远处的肿瘤。总之,由金属复合物介导的免疫调节和靶向干预是一种新的、有前景的肿瘤治疗方法。这为靶向治疗和免疫治疗的联合开发提供了有效的策略。
Endoplasmic reticulum-targeted iridium(III) photosensitizer induces pyroptosis for augmented tumor immunotherapy
An ideal tumor treatment strategy involves therapeutic approaches that can enhance the immunogenicity of the tumor microenvironment while simultaneously eliminating the primary tumor. A cholic acid-modified iridium(III) (Ir3) photosensitizer, targeted to the endoplasmic reticulum (ER), has been reported to exhibit potent type I and type II photodynamic therapeutic effects against triple-negative breast cancer (MDA-MB-231). This photosensitizer induces pyroptotic cell death mediated by gasdermin E (GSDME) through photodynamic means and enhances tumor immunotherapy. Mechanistic studies have revealed that complex Ir3 induces characteristics of damage-related molecular patterns (DAMPs) in MDA-MB-231 breast cancer cells under light conditions. These include cell-surface calreticulin (CRT) eversion, extracellular high mobility group box 1 (HMGB1) and ATP release, accompanied by ER stress and increased reactive oxygen species (ROS). Consequently, complex Ir3 promotes dendritic cell maturation and antigen presentation under light conditions, fully activates T cell-dependent immune response in vivo, and ultimately eliminates distant tumors while destroying primary tumors. In conclusion, immune regulation and targeted intervention mediated by metal complexes represent a new and promising approach to tumor therapy. This provides an effective strategy for the development of combined targeted therapy and immunotherapy.
期刊介绍:
The Journal of Inorganic Biochemistry is an established international forum for research in all aspects of Biological Inorganic Chemistry. Original papers of a high scientific level are published in the form of Articles (full length papers), Short Communications, Focused Reviews and Bioinorganic Methods. Topics include: the chemistry, structure and function of metalloenzymes; the interaction of inorganic ions and molecules with proteins and nucleic acids; the synthesis and properties of coordination complexes of biological interest including both structural and functional model systems; the function of metal- containing systems in the regulation of gene expression; the role of metals in medicine; the application of spectroscopic methods to determine the structure of metallobiomolecules; the preparation and characterization of metal-based biomaterials; and related systems. The emphasis of the Journal is on the structure and mechanism of action of metallobiomolecules.