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Machine learning-assisted SERS-based dual-aptamer biosensor for ultrasensitive clinical screening of breast cancer.

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Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy 📖 저널 OA 4.7% 2023: 0/1 OA 2024: 0/1 OA 2025: 0/13 OA 2026: 3/49 OA 2023~2026 2026 Vol.344(Pt 1) p. 126640
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Xia H, Xiong L, Huang R, Liu N, Muhammad M, Hong J

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Breast cancer remains a global health challenge, with an increasing number of cases necessitating innovative approaches to streamline patient management prior to treatment.

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APA Xia H, Xiong L, et al. (2026). Machine learning-assisted SERS-based dual-aptamer biosensor for ultrasensitive clinical screening of breast cancer.. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 344(Pt 1), 126640. https://doi.org/10.1016/j.saa.2025.126640
MLA Xia H, et al.. "Machine learning-assisted SERS-based dual-aptamer biosensor for ultrasensitive clinical screening of breast cancer.." Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, vol. 344, no. Pt 1, 2026, pp. 126640.
PMID 40627939 ↗

Abstract

Breast cancer remains a global health challenge, with an increasing number of cases necessitating innovative approaches to streamline patient management prior to treatment. In this study, we present a comprehensive aptamer-involved surface-enhanced Raman spectroscopy (aptamer-SERS)-based protocol specifically designed for large-scale clinical screening of the circulating protein MUC1 overexpressed in the majority of breast cancer cases. Central to our approach was a "sandwich" assay, where MUC1 was anchored between aptamer-functionalized bimetallic core-shell nanoparticles (NPs) and magnetic nanobeads. The biosensor was applied to monitor MUC1 in serum samples through SERS signals from the reporter molecule 4-ATP, exhibiting a strong linear correlation across a wide dynamic range and the lower the limit of detection (LOD) of 2.96 fg/mL. To support clinical decision-making, the protocol was integrated with a machine learning (ML)model for the classification of SERS signal patterns, demonstrating performance metrics of 96% accuracy and 93.7% specificity when applied to diverse serum samples. This integration enabled robust, non-invasive preclinical screening that informs therapeutic regulation and patient monitoring long before clinical symptoms present. By establishing a scalable framework for continuous monitoring of MUC1 levels across large populations, our study offered a forward-thinking tool, namely, dual-aptamer-SERS biosensor, that may optimize individualized treatment planning and improve overall clinical management strategies.

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