Yang Chao, Wang Wenkuan, Gao Yunhao, Yin Lu, Pan Kehao, Chen Dong, Yang Feiya, Xing Nianzeng
Department of Urology/State Key Laboratory of Molecular Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
ACS Appl Mater Interfaces. 2025 Feb 12;17(6):9125-9139. doi: 10.1021/acsami.4c20545. Epub 2025 Jan 30.
Sonodynamic therapy, a treatment modality recently widely used, is capable of disrupting the tumor microenvironment by inducing immunogenic cell death (ICD) and enhancing antitumor immunity during immunotherapy. Erdafitinib, an inhibitor of the fibroblast growth factor receptor, has demonstrated potential benefits for treating bladder cancer. However, Erdafitinib shows effectiveness in only a small number of patients, and the majority of patients responding positively to the medication have "immune-cold" tumors. To increase the therapeutic efficacy of Erdafitinib, we have herein developed a biodegradable pseudoconjugate polymer (PSP) with sonodynamic capabilities. Erdafitinib could be efficiently encapsulated in nanoparticles (NP-PE) prepared through the self-assembly of PSP with an oxidation-sensitive polymer (P1). Under ultrasound conditions, NP-PE effectively induced cytotoxicity by producing reactive oxygen species and further triggering ICD. Compared with Erdafitinib, NP-PE inhibited the expression of FGFR3 to a higher extent. In animal models with bladder cancer, NP-PE inhibited tumor growth, stimulated antitumor immunity, and synergized with antiprogrammed cell death-ligand 1 (aPD-L1), offering a novel approach for the treatment of bladder cancer.
声动力疗法是一种最近被广泛应用的治疗方式,它能够通过诱导免疫原性细胞死亡(ICD)来破坏肿瘤微环境,并在免疫治疗期间增强抗肿瘤免疫力。厄达替尼是一种成纤维细胞生长因子受体抑制剂,已显示出治疗膀胱癌的潜在益处。然而,厄达替尼仅在少数患者中显示出疗效,并且大多数对该药物有阳性反应的患者患有“免疫冷”肿瘤。为了提高厄达替尼的治疗效果,我们在此开发了一种具有声动力能力的可生物降解假共轭聚合物(PSP)。厄达替尼可以有效地封装在通过PSP与氧化敏感聚合物(P1)自组装制备的纳米颗粒(NP-PE)中。在超声条件下,NP-PE通过产生活性氧并进一步触发ICD有效地诱导细胞毒性。与厄达替尼相比,NP-PE对FGFR3表达的抑制程度更高。在膀胱癌动物模型中,NP-PE抑制肿瘤生长,刺激抗肿瘤免疫力,并与抗程序性细胞死亡配体1(aPD-L1)协同作用,为膀胱癌的治疗提供了一种新方法。