外体
唾液酸
卵巢癌
化学
纳米传感器
微泡
表面增强拉曼光谱
癌症研究
卵巢肿瘤
临床诊断
拉曼光谱
拉曼散射
纳米技术
前列腺癌
生物化学
生物物理学
纳米颗粒
癌症
计算生物学
分析物
上皮性卵巢癌
微泡
浆液性卵巢癌
作者
Lili Cong,Jiaqi Wang,Sijun Huang,Xiaxia Man,Yi Guo,Shuping Xu,Songling Zhang
标识
DOI:10.1002/advs.202518190
摘要
ABSTRACT Currently, the absence of ovarian cancer (OC)‐specific biomarkers impedes the development of precise noninvasive diagnostic and monitoring strategies. Exosomal surface sialic acid (SA), a key mediator of intercellular communication and disease progression, emerges as a promising biomarker, though its role in OC remains unclear. Conventional exosome isolation and detection methods exhibit limited clinical utility. Herein, we developed a CD63 aptamer‐functionalized gold array chip integrated with a surface‐enhanced Raman scattering (SERS) nanosensor for sensitive SA analysis. The chip efficiently isolated exosomes from clinical serum, while the nanosensor selectively bound exosomal SA via molecular recognition, thereby altering the SERS intensity ratio of the nanosensor. More importantly, machine learning can discern SA signatures from SERS spectra, achieving 93% accuracy in OC diagnosis. The longitudinal monitoring of SA throughout the entire treatment period (preoperative, postoperative, and chemotherapy) revealed a potential correlation with treatment response as indicated by clinical markers (CA125, HE4), demonstrating the utility of exosomal SA in precision treatment evaluation. This provides a powerful tool for the diagnosis and treatment monitoring of OC and plays a critical role in precision medicine.
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