神经鞘瘤
胶体金
2型神经纤维瘤病
神经纤维瘤病
化学
蛋白酶
细胞外基质
癌症研究
连接器
纳米颗粒
生物物理学
肽
基质金属蛋白酶
基质(化学分析)
肿瘤进展
生物医学工程
分子生物学
材料科学
劈理(地质)
体内
聚乙二醇
医学
前庭神经鞘瘤
病理
酶谱
作者
Shimayali Kaushal,Han T. N. Nguyen,Melanie Fisher,Hsuan-Chih Kuo,Zachary D. Schultz,Yin Ren
标识
DOI:10.1021/acsanm.5c04657
摘要
Neurofibromatosis type 2-related schwannomatosis (NF2-SWN) is a devastating genetic tumor-disposition syndrome characterized by multiple nervous system neoplasms. A hallmark of NF2-SWN is bilateral vestibular schwannomas (VSs) that cause hearing loss, vertigo, and life-threatening brainstem compression. Current imaging methods detect NF2-associated VS often late in their development and could lead to delayed therapeutic interventions. Matrix metalloproteinase-9 (MMP-9) is a key protease involved in extracellular matrix remodeling and tumor progression in NF2-associated VS, making it an attractive molecular target for activity-based sensing. Here, we develop MMP-9 activatable gold nanoparticles (AuNPs) incorporating a protease-cleavable peptide to enable sensitive reporting of protease activity in VS tissue. Through systematic tuning of polyethylene glycol (PEG) linker length and peptide valency, we establish an AuNP configuration that exhibits both efficient enzymatic cleavage and selectivity for MMP-9 over other VS-associated proteases. In schwannoma tissue, nanoparticles distinguish tumor from healthy nerve with >95% accuracy and detect 2 mm tumorscorresponding, based on published VS growth rates, to detection approximately 23 months earlier than conventional MRIenabling substantially earlier intervention. Longitudinal measurement of nanoparticle activation further resolves changes in MMP-9 activity within the tumor in response to therapeutic intervention, illustrating the platform's capacity in monitoring treatment response. Together, these findings establish MMP-9 activatable AuNP as a sensitive, spatially resolved diagnostic tool for NF2-SWN that complements imaging by directly quantifying protease activity in tumors that are inaccessible to biopsy.
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