Suppr超能文献

一种用于协同癌症免疫治疗的诱导焦亡的三价砷纳米胶束平台。

A Pyroptosis-Inducing Arsenic(III) Nanomicelle Platform for Synergistic Cancer Immunotherapy.

作者信息

Wang Xing, Tang Yuqi, Li Yuanhang, Qi Zhengjian

机构信息

School of Chemistry and Chemical Engineering, Southeast University, Nanjing, 211189, P. R. China.

Institute of Advanced Materials, School of Chemistry and Chemical Engineering, Southeast University, Nanjing, 211189, P. R. China.

出版信息

Adv Healthc Mater. 2024 Dec;13(30):e2401904. doi: 10.1002/adhm.202401904. Epub 2024 Aug 5.

Abstract

Immunogenic cell death (ICD) could activate anti-tumor immune responses, which is highly attractive for improving cancer treatment effectiveness. Here, this work reports a multifunctional arsenic(III) allosteric inhibitor Mech02, which induces excessive accumulation of O through sensitized biocatalytic reactions, leading to cell pyroptosis and amplified ICD effect. After Mech02 is converted to Mech03, it could actualize stronger binding effects on the allosteric pocket of pyruvate kinase M2, further interfering with the anaerobic glycolysis pathway of tumors. The enhanced DNA damage triggered by Mech02 and the pyroptosis of cancer stem cells provide assurance for complete tumor clearance. In vivo experiments prove nanomicelle Mech02-HA NPs is able to activate immune memory effects and raise the persistence of anti-tumor immunity. In summary, this study for the first time to introduce the arsenic(III) pharmacophore as an enhanced ICD effect initiator into nitrogen mustard, providing insights for the development of efficient multimodal tumor therapy agents.

摘要

免疫原性细胞死亡(ICD)可激活抗肿瘤免疫反应,这对于提高癌症治疗效果极具吸引力。在此,本研究报告了一种多功能砷(III)变构抑制剂Mech02,它通过敏化生物催化反应诱导O的过度积累,导致细胞焦亡并放大ICD效应。Mech02转化为Mech03后,可对丙酮酸激酶M2的变构口袋实现更强的结合作用,进一步干扰肿瘤的无氧糖酵解途径。Mech02引发的增强的DNA损伤和癌症干细胞的焦亡为完全清除肿瘤提供了保证。体内实验证明纳米胶束Mech02-HA NPs能够激活免疫记忆效应并提高抗肿瘤免疫的持久性。总之,本研究首次将砷(III)药效基团作为增强ICD效应的引发剂引入氮芥,为开发高效的多模式肿瘤治疗药物提供了思路。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验