# Machine Learning‐Enhanced Analysis of Exosomal Surface Sialic Acid Using Surface‐Enhanced Raman Spectroscopy for Ovarian Cancer Diagnosis and Therapeutic Monitoring

**Authors:** Lili Cong, Jiaqi Wang, Sijun Huang, Xiaxia Man, Yi Guo, Shuping Xu, Songling Zhang

PMC · DOI: 10.1002/advs.202518190 · Advanced Science · 2026-01-21

## TL;DR

This paper introduces a machine learning-enhanced method using Raman spectroscopy to analyze exosomal sialic acid for diagnosing ovarian cancer and monitoring treatment response.

## Contribution

A CD63 aptamer-functionalized gold chip with a SERS nanosensor and machine learning for sensitive and accurate exosomal sialic acid analysis in ovarian cancer.

## Key findings

- The method achieved 93% accuracy in diagnosing ovarian cancer using machine learning on SERS spectra.
- Exosomal sialic acid levels correlated with treatment response across preoperative, postoperative, and chemotherapy stages.
- The approach offers a noninvasive tool for ovarian cancer diagnosis and precision treatment monitoring.

## 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.

Machine learning‐assisted surface‐enhanced Raman spectroscopy analysis of exosomal sialic acid for ovarian cancer diagnosis, as well as independent monitoring of exosomal sialic acid expression levels across different treatment periods, reveals a potential correlation with treatment response.

## Linked entities

- **Proteins:** CD63 (CD63 molecule)
- **Chemicals:** sialic acid (PubChem CID 445063)
- **Diseases:** ovarian cancer (MONDO:0005140)

## Full-text entities

- **Genes:** WFDC2 (WAP four-disulfide core domain 2) [NCBI Gene 10406] {aka BENP, EDDM4, HE4, WAP5, dJ461P17.6}, CD63 (CD63 molecule) [NCBI Gene 967] {aka AD1, HOP-26, ME491, MLA1, OMA81H, Pltgp40}, MUC16 (mucin 16, cell surface associated) [NCBI Gene 94025] {aka CA125}
- **Diseases:** OC (MESH:D010051)
- **Chemicals:** gold (MESH:D006046), SA (MESH:D019158)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13042971/full.md

## References

62 references — full list in the complete paper: https://tomesphere.com/paper/PMC13042971/full.md

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Source: https://tomesphere.com/paper/PMC13042971