癌症研究
免疫疗法
骨肉瘤
渗透(HVAC)
Pet成像
上睑下垂
糖酵解
正电子发射断层摄影术
体内
化学
Hsp90抑制剂
免疫原性
恶性肿瘤
医学
边距(机器学习)
抑制器
细胞
肿瘤细胞
放射治疗
作者
Kaiyuan Liu,Ruotong Li,Li Zhang,Hengli Lu,Binhui Yang,Qian Hu,Yining Tao,Haoran Mu,Jing Han,Pengfei Zan,Jiakang Shen,Dongqing Zuo,Hongsheng Wang,Wei Sun,Xingjun Zhu
标识
DOI:10.1002/advs.202516035
摘要
In advanced osteosarcoma, tumor invasion often prevents complete resection, and immunotherapy is limited by the tumor's immunosuppressive nature, making residual lesions a key source of recurrence. To address this, we developed an ALP-responsive theranostic nanoplatform (SGPF) integrating an AIEgens (STEA) and HSP90 inhibitor (Ganetespib) for imaging-guided resection and multimodal therapy. Selenium-doped STEA enables NIR-IIb imaging and enhanced phototherapy via narrowed HOMO-LUMO gaps and nonradiative decay optimization. At tumor sites, ALP-triggered nanomicelle cleavage releases STEA and Ganetespib while vaporizing perfluorohexane to relieve hypoxia. NIR irradiation induces pyroptosis via caspase-3/GSDME activation and immunogenic cell death, while Ganetespib suppresses glycolysis (HK2/PKM2 downregulation) to reverse lactate-driven immunosuppression. This dual-action strategy synergistically enhances T-cell infiltration and ablates residual/metastatic lesions, offering a transformative approach for unresectable Osteosarcoma.
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